Jose L. Martinez - Amner Muñoz-Acevedo - Mahendra Rai - Ethnobotany - Local Knowledge and Traditions-CRC Press (2019)
Jose L. Martinez - Amner Muñoz-Acevedo - Mahendra Rai - Ethnobotany - Local Knowledge and Traditions-CRC Press (2019)
Editors
José L. Martinez
Vice Rectory of Research
Development and Innovation
Universidad de Santiago de Chile
Santiago, Chile
Amner Muñoz-Acevedo
Chemistry and Biology Research Group
Department of Chemistry and Biology
Universidad del Norte
Barranquilla, Colombia
Mahendra Rai
Department of Biotechnology
SGB Amravati University
Amravati, Maharashtra, India
p,
p,
A SCIENCE PUBLISHERS BOOK
A SCIENCE PUBLISHERS BOOK
Cover credit: Reproduced by kind courtesy of Prof. Amner Muñoz-Acevedo (co-editor)
CRC Press
Taylor & Francis Group
6000 Broken Sound Parkway NW, Suite 300
Boca Raton, FL 33487-2742
Except as permitted under U.S. Copyright Law, no part of this book may be reprinted, reproduced, transmitted,
or utilized in any form by any electronic, mechanical, or other means, now known or hereafter invented, includ-
ing photocopying, microfilming, and recording, or in any information storage or retrieval system, without written
permission from the publishers.
For permission to photocopy or use material electronically from this work, please access www.copyright.com
(http://www.copyright.com/) or contact the Copyright Clearance Center, Inc. (CCC), 222 Rosewood Drive, Danvers,
MA 01923, 978-750-8400. CCC is a not-for-profit organization that provides licenses and registration for a variety
of users. For organizations that have been granted a photocopy license by the CCC, a separate system of payment
has been arranged.
Trademark Notice: Product or corporate names may be trademarks or registered trademarks, and are used only for
identification and explanation without intent to infringe.
The local knowledge or indigenous knowledge of the use of plants is based on the
wisdom and experience of the local community since ancient time. In due course
of time, this knowledge becomes the tradition of the local community or tribes.
Such knowledge is passed from one generation to another generation and is applied
in agriculture, medicines and other household activities. In the past decade, the
botanists have made tremendous efforts to gather this knowledge, and eventually,
a new branch of botany known as ‘Ethnobotany’ has originated.
Ethnobotany has always been used as primary source to search biologically
active molecules (ca. 60%) from nature and at the same time, it has contributed to
the development of drugs (pharmaceutical industry) that have improved the quality
of human life. However, some active constituents found within those plants are
not the result of the scientific validations based on traditional medicinal uses of
plants containing them. On the other hand, there are a few documents/books on
ethnobotany (e.g., WHO monographs) containing information about plant-based
treatment for specific chronic diseases such as hypertension, cancer, CNS disorders,
psoriasis, and urolithiasis, etc.
Most of the plants described in the present book have been used in traditional
medicine by local community for specific ailments and the biological activities
related to each “sickness” have been scientifically verified.
We hope that the present book will be an appropriate consultation tool for
scientists/professionals/experts such as ethnobotanists, botanists, cell/molecular
biologists, chemists, pharmacists, pharmacologists, and environmentalists/
ecologists. It will also be useful for undergraduate and postgraduate students from
the same areas and for the pharmaceutical industries.
José L. Martinez
Amner Muñoz-Acevedo
Mahendra Rai
Contents
Preface iii
1. Mururé (Brosimum acutifolium Huber) in the Treatment of 1
Syphilis in Colonial Amazonia: From Historical Data to the
Actual Contribution in Treatment
Erika Fernanda de Matos Vieira, Maria da Graça Ribeiro Campos
and Flávia Cristina Araújo Lucas
2. Agroecology, Local Knowledge and Participatory Research: 19
Articulation of Knowledge for Sustainable Use of Plant
Resources in Agroecosystems
Santiago Peredo Parada and Claudia Barrera
3. The Path of Ethnopharmacobotany: From Economic Botany 34
to Ethnobotany
Marcelo L. Wagner, Leonardo M. Anconatani, Rafael A. Ricco,
Beatriz G. Varela and Gustavo C. Giberti
4. Patagonian Berries: An Ethnobotanical Approach to Exploration 50
of their Nutraceutical Potential
Melina F. Chamorro, Ana Ladio and Soledad Molares
5. Status of Research on Medicinal Plants in the Cajamarca’s 70
Region, Peru
Juan F. Seminario Cunya, Berardo Escalante Zumaeta and
Alejandro Seminario Cunya
6. Recent Reports on Ethnopharmacological and Ethnobotanical 90
Studies of Valeriana carnosa Sm. (Valerianaceae)
Soledad Molares, Ana H. Ladio and Nicolás Nagahama
7. Traditional Knowledge of Antivenom Plants: Bioactive 103
Compounds and Their Antiophidic Properties
Carolina Alves dos Santos, Marco V. Chaud, Valquíria Miwa Hanai Yoshida,
Raksha Pandit, Mahendra Rai and Yoko Oshima-Franco
vi ETHNOBOTANY: Local Knowledge and Traditions
Introduction
Studying the historical ethnobotany of medicinal plants is a new method of
obtaining information about plants and people derived from historical records,
including documents about botany, anthropology, ecology, and history that are still
used and relevant today (Prance 2000, Medeiros 2009). Living and learning with
diverse ethnic groups have provided valuable contributions to the development of
research about natural products, as well as knowledge about the close relationship
The aim of this chapter is to share a case study that can be used as an example
of the tools and the various steps that should be followed in ethnobotanical research.
Based on this, the ethnopharmacology of mururé since the 18th century for the
treatment of syphilis will be described. A correlation of the past-present therapeutic
use and contribution of historical records in the use of natural products will also
be discussed.
This was interpreted as an indicator of the effect of the medicinal plant. Similar
urinary tract laden with concentrated sediments also occurs when syphilis patients
use current medicines for this pathology (Neves and Araújo 2013, Anvisa 2016b).
Other effects noted were neurological disorders described by the priest as chills,
tremors, and seizures that arise immediately after ingestion, which were treated
by placing a warm cloth on the stomach.
João Daniel also verified the performance of the plant for cases of neurosyphilis,
which could appear in 12 to 18 months after infection and could be asymptomatic.
He noted a small amount is enough to get rid of the disease and bad mood from
the bones and nerves in one night (“[...] e basta esta pequena quantidade para
dos mesmos ossos e nervos arrancar em uma noute toda doença, e mau humor”).
For neurosyphilis, Vargas et al. (2000) affirmed the strong psychological effect on
the patient, and Barros et al. (2005) characterized it as an infection that affects the
nervous system and can cause lesions on the brain and spinal cord. These clinical
observations were similar to what the Father reported. Neurosyphilis had great
repercussions before the use of penicillin and resurged in the late 20th century,
mainly in HIV patients who were more susceptible to the disease (Neves and Araújo
2013, Caixeta et al. 2014).
Mururé was also prescribed for other illnesses: it treated alporcas, and all
the Gallic diseases “[...] Da mesma sorte cura alporcas, e todas as doenças que
pecam de gálico” (Daniel 2004). Alporca is a term that signifies scrofula, where
there is swelling in the lymph nodes, and is associated with tuberculosis (Sayahi
and Thomas 2005, Capone 2006, Almeida 2012). Carrara (1996) reported that in
the past syphilis was considered by the medical community as an aggravating agent
of tuberculosis. Evidence of this was reported after Father started administering
the milk when there were clinical symptoms of tuberculosis and considered the
treatment very effective.
The experience and effectiveness of using mururé in the missions, on both
Indians and Caucasians, impressed João Daniel who soon saw the export potential
of the species to use as a medicine in Europe. Introducing this plant to Europe would
be the beginning of its wide dissemination throughout the world. The articulation
of knowledge, healing practices, and market views by the Jesuits was discussed
by Pinto (2005), who analyzed the transfer of natural resources and traditional
knowledge to other parts of the world and promoted advances in the sciences
(Calainho 2005, Medeiros 2009, Laws 2013). In relation to this, João Daniel was
a visionary by promoting the value and use of the riches in the region. Studying
mururé and other plants did not simply occur because people were searching for
knowledge about specific plant species, but was instead driven by the fact that these
plants were potentially useful to the colony and cities abroad (Costa 2007, Santos
2013, São Bento and Santos 2015).
Based on tests using mururé to treat syphilis in the 20th century, in the year
1918 there was an elevated number of reported cases (about 6 million people) of
the disease throughout the country. Due to this health crisis, drugstores popularized
Mururé in the Treatment of Syphilis 5
Fig. 1.1. Advertisement for syphilis treatment using mururé in a magazine published in 1918. Source:
Revista Careta, 1918, edition 502.
Fig. 1.2. Advertisement for syphilis treatment using mururé in a magazine published in 1918. Source:
Revista Careta, 1918, edition 501.
6 ETHNOBOTANY: Local Knowledge and Traditions
a medicinal product in the largest open fair in Latin America, Ver-o-Peso Fair in
Belém, Pará (Iphan 2017), with similar indications as the historical records from
the 18th century and the 1918 advertisements (Fig. 1.3). The herbalists at Ver-o-
Peso, who are considered holders and transmitters of traditional knowledge in an
urban environment (Dantas and Ferreira 2013), continue to promote mururé as a
curative and therapeutic product for syphilis.
Fig. 1.3. Mururé bark for sale by herbalists at the Ver-o-Peso Fair in 2017.
source of this study. Father Daniel was a naturalist, who wrote this work in Lisboa
while in prison (due to Pombaline orders), which became a massive codex that is
considered by many historians as a significant document about Amazonia during
the colonial period (Salles 2004). It is the most comprehensive record and most
complete source of knowledge about Amazonia during the 18th century because
the information in it is the result of extensive fieldwork and vast cataloging of data,
especially about the flora of the region (Siewierski 2014). According to Tocantins
(1976), although there are other publications in the same genus, this book is the
“Ecological bible of Amazonia,” and is a complete, well-researched work about
the region produced by a member of the Society of Jesus.
Species definition
The species was identified using the taxonomic clues method in Identificação de
termos oitocentistas relacionados às plantas medicinais usadas no Mosteiro de
São Bento do Rio de Janeiro, Brasil, by Medeiros (2010). To properly confirm the
8 ETHNOBOTANY: Local Knowledge and Traditions
scientific nomenclature, the following criteria were used: (1) text search of the
common name “moruré” and “mururé”; (2) detailed examination of morphological
descriptions and life form of mururé, both by the Father and other authors; (3)
confirmation of the botanical identification using scientific articles and specimens
listed in virtual herbaria (www.tropicos.org) and the “List of Species of Flora of
Brazil” in “Flora do Brasil 2020 Project” (floradobrasil.jbrj.gov.br)”.
For the writing in older works, spelling and punctuations were modified based
on the current norms for Portuguese. Transcription into Portuguese and identifying
characteristic linguistic terms of the period were based on Estratégia e Táctica da
Transcrição (Castro and Ramos 1986). For quotes by some authors, the vocabulary
used was absolutely respected.
commercialization because they were rare, came from America, and could boost
the economy of the 18th century.
The advancement of religious and exploratory missions in Amazonia favored
greater rapprochement and contact between different peoples and ethnicities. This
period, comprising the 18th century, recorded significant documentary data about
diseases of various natures that proliferated during these encounters (Veríssimo and
Pereira 2014). Sexually transmitted diseases, such as syphilis, became worrying
and resulted in strong social consequences that included a change in behavior in
the population, for example, the use of condoms made of sheep intestines (Veloso
2001). Guilherme Piso, in História Natural do Brasil Ilustrada (1648), highlighted
the venereal evil (“mal venéreo”) in Africans, Indians, Dutch and Portuguese due
to contagion from intercourse. He considered this disease as endemic to the region
and noted the efficiency of treating it with indigenous remedies (“[...] sara logo,
só com os remédios indígenas”).
The increased incidence of diseases resulted in a search for treatments using
tests and formulas with therapeutic plants, which took place at houses built by the
Jesuits near forests. According to Father João Daniel (1722–1776), the traditional
pharmacies of the Jesuits were supplied with precious woods, miraculous barks,
large forests of copaiba, umeri balsams, and the leaves and bark of cinnamon
and quina, among other plants. This allowed them to take advantage of these
natural resources and, with the help of the American Indians that were deeply
knowledgeable about the forest and extremely skilled at extracting the resources,
to use medicines in the missions and give them to white settlers so they would be
sent to Europe where they were needed (Daniel 2004).
The commercial potential of Amazonian natural products was frequently
valorized by João Daniel who, according to Pinto (2005), had a very peculiar
intellectual and scientific vision for the formation of the missionaries that made
up the religious order due to the importance of this knowledge as a mechanism of
exploitation and power.
Fig. 1.4. Specimen of mururé, donated by the “Rio de Janeiro Botanical Garden” to “The New York
Botanical Garden”, collected in the state of Pará in 1927 (Source: www.nybg.org).
average temperature is between 22°C and 30°C, and prefers sandy and clayey sand
soils with an average amount of organic matter (Revilla 2001, apud Pinagé 2011).
process, especially because of the diversity of plants. In this context, the present
traditional and popular knowledge, as well as information from communities that
have produced this type of knowledge in the past, remain valuable resources for
identifying medicinally useful plants (Pereira and Cardoso 2012, Medeiros 2009).
Ratifying this, the WHO (2011) reported that the amount of modern medicines from
plants is significant and could reach 60% for antitumor and antibacterial drugs.
Mururé (Brosimum acutifolium Huber), despite being used for other purposes
(e.g., in cosmetics and food), is mostly employed medicinally because its latex
and bark efficiently act against many illnesses and its sap has antiarthritic and
antisyphilitic properties (Rodrigues 1989, Pinagé 2011). For treating syphilis,
a daily dose of the sap should be used that does not exceed 8 g since an excess
amount produces side effects, such as joint pain, polyuria (increased amount of
urine), nausea and dizziness; however, literature also mentions the use of the bark
prepared as a tea (Matta 2003, apud Pinagé 2011), contrary to João Daniel who
only mentioned the sap.
Works reported the use of the species in Amazonian communities. According
to Coelho-Ferreira et al. (2005), B. acutifolium is one of the 228 species that
comprise the phytopharmacopoeia of the Marudá fishing community in the interior
of Pará. In addition, Monteles and Pinheiro (2007) documented its use as a blood
purifier (by preparing bottles with its bark) by a Quilombola community in the
municipality of Presidente Juscelino which, according to IBGE (2016), is part of
Maranhão in Amazonia.
In pharmacological studies, the flavonoid BAS1 (4’-hydroxy,7,8-(2’’,2”-
dimethyl-pyran)-flavan) was isolated from Brosimum acutifolium (Moraes 2011).
In this work, the mechanism of anti-inflammatory action of BAS1 in stimulated
murine macrophages was characterized. The results demonstrated that BAS1, at
high concentrations, had a cytotoxic effect. In addition, there was a reduction in
the factors leading to inflammation and the flavonoid exhibited anti-inflammatory
activity.
The antiproliferative and antineoplastic activities of four flavonoids
from B. acutifolium were investigated by Maués (2013), who isolated
two flavans, 4’-hydroxy-7,8-(2”,2”-dimethylpyran)-flavan (BAS-1) and
7,4’-dihydroxy-8,(3,3-dimethylallil)-flavan (BAS-4), and two chalcones,
4,2’-dihydroxy-3’,4’-(2”,2”-dimethylpyran)-chalcone (BAS-6) and
4,2’,4’-trihydroxy-3’-(3,3-dimethylallil)-chalcone (BAS-7), and verify the effects
on rat glioblastomas in vitro. The study concluded that the BAS-1, BAS-4 and
BAS-7 flavonoids had antineoplastic potential as an agent in therapy, and that the
BAS-4 flavonoid was the most promising because its action on tumor cells was
more efficient and its cytotoxic activity was the least harmful to healthy cells.
Other studies indicated the presence of various flavonoids in the bark of mururé
(Torres et al. 2000, Takashima and Ohsaki 2002, Takashima et al. 2005). The latter
study evaluated the activity of four flavonoids against leukemia cells, which had a
cytotoxic effect on cells resistant to vincristine (the drug used to treat the illness).
12 ETHNOBOTANY: Local Knowledge and Traditions
Thus, some chemicals’ structures of the isolated compounds from mururé sap/bark,
e.g., flavans (BAS-1, and BAS-4), and chalcone (BAS-7) can be seen.
Baptista (2007), did ethnobotanical studies in the interior of Amazonia,
as “Selected Concentrated Brosimum acutifolium (SCBA)”, and used the sap
for phytochemical experiments testing the antinociceptive (analgesia) and
antiedematogenic actions in mice. This work reported that at certain doses SCBA
prevented the development of edema in mices. The study also investigated the
phytochemical constituents of B. acutifolium latex and found the presence of
saponins, proteins and amino acids, phenols, and alkaloids. The results demonstrated
that the analgesia promoted by SCBA is due to one or more secondary metabolites,
such as saponin, which exhibit anti-inflammatory activity. The anti-oedematous
activity was verified and explained by the action of the sap on the chemical mediators
that promote an inflammatory state. According to Cruvinel et al. (2010), edema is
a clinical sign of inflammation.
Baptista (2007) also studied the acute and sub-acute toxicity and the metabolites
present in mururé bark. The work identified saponins that damage cells by altering
the permeability of membranes, which destroys them. This type of alteration can
be explained by the amphiphilic behavior of saponins, which can form complexes
with steroids, proteins and membrane phospholipids that have a variable number of
biological properties, including actions on cell membranes (Schenkel et al. 2004).
In a study about takini, a hallucinogen used by shamans in Amazonia that is
prepared from the sap of B. acutifolium, Moretti et al. (2006) identified the presence
of the alkaloid bufotenin (5-hydroxy-dimethyltryptamine) that is a compound with
psychotrophic properties. This alkaloid is present in other species of Brosimum as
B. utile (Kunth) Pittier and has been studied for its antifungal and antibacterial
activities due to the toxic effect on the DNA of microorganisms (Haro 2015,
Manotoa 2015).
Overall, saponins are important because in addition to their action on
membranes, they help in the absorption of other compounds, which increases the
immune response (Schenkel et al. 2004), and the alkaloid bufotenine promotes
bactericidal activity.
Conclusions
Current treatment methods for syphilis mostly involve the use of penicillin with
no reference of using Brosimum acutifolium, although there are historical medical
records that note mururé is effective. The search for new medicines and the value
of Father João Daniel’s documents are evidence of the great naturalistic ability of a
plant that, due to the success of its medicinal effects, elevated mururé in the Tesouro
Descoberto do Máximo Rio Amazonas to the potential drug category. Countries that
currently lead the world in syphilis cases and suffer from elementary social problems
(e.g., related to the production and distribution of medicines) should note this fact.
The search for medicinal properties in plants as a solution to the unavailability
of medicine, mainly using past evidence, strengthens the relationship between
people and plants, and is important to science today. The analysis made in this work
show that the study of historical documents can be an important tool to develop
medicine because these works are potential resources to find new drugs.
Mururé in the Treatment of Syphilis 15
References
Almeida, L.F. 1976. Aclimatação de plantas do Oriente no Brasil durante o século XVII e XVIII. Revista
portuguesa de História. 15: 339–431.
Almeida, M.A.P. 2012. O Porto e as epidemias: saúde e higiene na imprensa diária em períodos de crise
sanitária, 1854–56, 1899 e 1918. Revista de História da Sociedade e da Cultura 12: 371–391.
Avelleira, J.C.R. and Botino, G. 2006. Sífilis: Diagnóstico, tratamento e controle. An. Bras. Dermatol.
81: 111–126.
Anvisa. 2016a. III Antimicrobianos - principais grupos disponíveis para uso clínico: ß-Lactâmicos
– Penicilinas: Propriedades Farmacológicas. http://www.anvisa.gov.br/servicosaude/controle/
rede_rm/cursos/rm_controle/opas_web/modulo1/penicilinas2.htm Consultado em: 11 de outubro
de 2016.
Anvisa. 2016b. III Antimicrobianos - principais grupos disponíveis para uso clínico: ß-Lactâmicos –
Penicilinas: Efeitos colaterais. http://www.anvisa.gov.br/servicosaude/controle/rede_rm/cursos/
rm_controle/opas_web/modulo1/penicilinas10.htm Consultado em: 11 de outubro de 2016.
Anvisa. 2016c. III Antimicrobianos - principais grupos disponíveis para uso clínico: ß-Lactâmicos –
Penicilinas: Indicações clínicas. http://www.anvisa.gov.br/servicosaude/controle/rede_rm/cursos/
rm_controle/opas_web/modulo1/penicilinas6.htm Consultado em: 09 de outubro de 2016.
Anvisa. 2016d. Anvisa. III Antimicrobianos - principais grupos disponíveis para uso clínico: ß. http://
www.anvisa.gov.br/servicosaude/controle/rede_rm/cursos/rm_controle/opas_web/modulo1/
penicilinas10.htm Consultado em: 11 de outubro de 2016.
Baptista, E.R. 2007. Conhecimentos e práticas de cura em comunidades rurais amazônicas: recursos
terapêuticos vegetais. Tese de Doutorado. Universidade Federal do Pará, Brasil.
Barros, A.M., Cunha, A.P., Lisboa, C., Sá, M.J. and Resende, C. 2005. Neurossífilis: Revisão Clínica
e Laboratorial. ArquiMed. 19: 121–129.
Bessa, N.F.G., Borges, J.C.M., Beserra, E.P., Carvalho, R.H.A., Pereira, M.A.B., Fagundes, R. Campos,
S.L., Ribeiro, L.U., Quirino, M.S., Chagas Junior, A.F. and Alves, A. 2013. Prospecção fitoquímica
preliminar de plantas nativas do cerrado de uso popular medicinal pela comunidade rural do
assentamento vale verde – Tocantins. Rev. Bras. Plantas Med. 15: 692–707.
Berg, C.C. and DeWolf, G.P. 1975. Moraceae. pp. 173–299. In: Lanjouw, J. and Stoffers, A.L. (eds.).
Flora of Suriname. Vol. 5. Part 1. E.J. Brill, Leiden, Holanda.
Brasil. Ministério da Saúde. Secretaria de Vigilância em Saúde. Programa Nacional de DST e Aids.
2006. Manual de Bolso das Doenças Sexualmente Transmissíveis. Brasília, Brasil.
Brasil. Ministério da Saúde. 2010. Caderno 6: Aids, Hepatites Virais, Sífilis Congênita e Sífilis
em Gestantes. pp. 1–60. In: Brasil. Ministério da Saúde. Secretaria de Vigilância em Saúde.
Departamento de Vigilância Epidemológica. Guia de Vigilância Epidemiológica. Brasília.
Brasil. Ministério da Saúde. 2012. Práticas Integrativas e Complementares: Plantas Medicinais e
Fitoterapia na Atenção Básica. Ministério da Saúde, Brasília, Brasil.
Brasil. Ministério da Saúde. Secretaria de Vigilância em Saúde. 2015a. Departamento de DST, Aids
e Hepatites Virais. Boletim Epidemiológico: Sífilis 2015. Ministério da Saúde, Brasília, Brasil.
Brasil. Ministério da Saúde. Secretaria de Vigilância em Saúde. 2015b. Nota Informativa Conjunta nº
109/105/GAB/SVS/MS, GAB/SCTIE/MS. Ministério da Saúde, Brasília, Brasil.
Brasil. Ministério da saúde. 2016. Portal da Saúde, Ministério da Saúde - Tratamento. http://portalsaude.
saude.gov.br/index.php/tratamento Consultado em: 11 de outubro de 2016.
Capone, D., Mogami, R., Lopes, A.J., Tessarollo, B., Cunha, D.L., Capone, R.B., Siqueira, H.R. and
Jansen, J.M. 2006. Tuberculose Extrapulmonar. Revista Hope 5: 54–67.
Caixeta, L., Soares, V.L.D., Reis, G.D., Costa, J.N.L. and Vilela, A.C.M. 2014. Neurosífilis: Uma Breve
Revisão. Rev. Soc. Bras. Med. Trop. 43: 121–129.
Calainho, D.B. 2005. Jesuítas e Medicina no Brasil Colonial. Tempo 10: 61–75.
Carrara, S. 1996. Tributo a vênus: a luta contra a sífilis no Brasil, da passagem do século aos anos 40.
Editora Fiocruz, Rio de Janeiro, Brasil.
Castro, I. and Ramos, M.A. 1986. Estratégia e Táctica da Transcrição. pp. 99–122. In: Critique Textuelle
Portugaise, Actes du Coloque. Fondation Calouste Gulbenkian, Paris, França.
Costa, K.S. 2007. Natureza, colonização e utopia na obra de João Daniel. Hist. Cienc. Saúde Manguinhos
14: 95–12.
16 ETHNOBOTANY: Local Knowledge and Traditions
Veríssimo, T.C. and Pereira, J. 2014. Floresta Habitada: História da ocupação humana na Amazônia.
Imazon, Belém, Brasil.
Viegas Júnior, C., Bolzani, V.S. and Barreiro, E.J. 2006. Os produtos naturais e a química medicinal
moderna. Quím. Nova 29: 326–337.
World Health Organization. 2011. The world medicines situation 2011: traditional medicines: global
situation issues and challenges. Who, Geneva, Suiça.
World Health Organization. 2016. Who guidelines for the treatment of Treponema pallidum (syphilis).
Who, Geneva, Suíça.
WRB. 1918. Careta. Ano IX. Edição 501. Rio de Janeiro, Brasil.
WRB. 1918. Careta. Ano IX. Edição 552. Rio de Janeiro, Brasil.
CHAPTER 2
Introduction
Sustainable management and conservation of natural resources fulfill the
requirements of the rural communities involved and the necessities of the joint
work among the different actors of a territory. For that, it is imperative to use an
integrated approach, with established strategies allowing the deployment of all the
ecological and social-cultural potential that a community has in the environment
in which it is developed.
In this context, the local knowledge of peasants is fundamental because it
represents a collective learning process mediated by the environment in which they
live. This experiential knowledge has allowed, many times, to develop survival
strategies based on the multifunctionality of their farms as a result of their capacity
for cognitive adaptation.
Hence, it is necessary to promote space for the active participation of people
through dynamic processes in which individuals are part of the decisions that affect
them. Participatory research constitutes a methodology that seeks the participation
of the community for its own benefit establishing a new relationship between
theory and practice.
1
Department of Agricultural Management, Universidad de Santiago de Chile, Chile.
2
Agroecology and Environment Group, Universidad de Santiago de Chile, Chile.
* Corresponding author: [email protected]
20 ETHNOBOTANY: Local Knowledge and Traditions
4. The experimental nature of traditional knowledge based not only on the acute
observation but also on the experimental learning, such as the selection of seed
varieties for specific environments, new agricultural methods to overcome
the biological or socioeconomic particular limitations, among many others.
The characteristic of local knowledge pointed out by Gómez-Benito (2001)
shows the close relation between the local culture and its environment that, through
the appropriation processes of nature, has been configuring new landscapes evident
in highly complex agroecosystems. However, this knowledge is not the result of
a merely empirical exercise, but rather as a multipurpose strategy that seeks to
maximize the benefit of the social group and thereby guarantee the conditions,
allowing its social and material reproduction. As stated by van der Ploeg (1990),
this knowledge has an internal organization. This local knowledge is transferred by
way of language (Toledo and Barrera-Nassols 2008) and therefore, it is transmitted
along the spatio-temporal structure using a different logic, that is, the orality.
In the second stage, the interviews are performed with specific members of
the community, chosen for the detailed and precise knowledge they have about
the attributes of the species of interest for the community. The application of this
technique (in-depth interviews) is recommended among older adults (men/women)
as it allows the establishment of symmetrical relationships enriching the horizontal
dialogue, thereby expanding the research scope on the “secrets” of local wisdom.
Using the aforementioned methodological strategy allows an approach to
work with agricultural communities in order to diagnose its biocultural potential;
24 ETHNOBOTANY: Local Knowledge and Traditions
the manner in which these techniques are articulated enables the expansion of the
known and unknown information by the different members of the community. The
simultaneity in the application of the techniques, in addition, allows to connect and
complement the quantitative antecedents with those of qualitative nature. On the
other hand, the complementarity of the techniques (in quali- and quantitative terms)
permits to extend the previously established attributes (characteristics, variables)
of the study. The combination of the techniques, consequently, is indispensable
insofar as the agroecosystem is an agrarian unit where both sociocultural and
biophysical elements converge.
It is convenient to reinforce that in the proposed methodology the main actors
are the community members, which acquire a decisive role for the achievement of
the final objectives through the execution of concrete actions. The methodological
design, therefore, requires that the strategies be established, adjusted, and modified
as a result of this interaction and as an emerging product during the development
of the research (Peredo and Barrera 2002a). Pursuant to Guber (2004), the research
process is flexible, creative, and heterodox because it is joined to the constant and
parallel relationship between observation and elaboration, obtaining information
and data analysis. This process generates new concepts and explanatory connections
based on initial assumptions, which are reformulated and enriched by the actors’
categories and contextualized in the social life. For this, times and spaces are made
more flexible by obeying the reason (rationality) of life in the countryside (Toledo
1993), where the different tasks and the time distribution are managed on the basis
of the daily activity of each one.
DM CP ME EE P TA CF ADF NDF
M SD M SD M SD M SD M SD M SD M SD M SD M SD
Shoot 39.95 1.52 a 7.76 0.15 a 2.49 0.02 a 2.36 0.07 a 0.13 0.004 a 11.11 0.45 a 23.53 0.56 a 32.91 0.92 a 39.42 0.82 a
Leaf 39.49 1.52 a 8.72 0.25 b 2.68 0.03 b 2.78 0.25 a 0.15 0.004 b 13.34 0.68 a 19.15 0.68 b 32.38 0.82 a 36.68 0.18 a
Steam 46.53 1.08 b 5.03 0.10 c 1.94 0.05 c 2.28 0.27 a 0.10 0.01 c 5.33 0.22 b 35.97 1.06 c 46.38 0.25 c 57.15 0.21 c
Mean Value 41.78 1.06 7.23 0.36 2.38 0.07 2.46 0.12 0.13 0.01 10.04 0.78 25.95 1.62 35.09 1.64 42.15 2.32
DM = dry matter; CP = crude protein; ME = metabolizable energy; EE = ether extract; P = phosphorus; TA = total ash; CF = fiber crude; ADF = acid detergent fiber;
NDF = neutral detergent fiber. a, b, c: significantly different (p ≤ 0.05). M = mean; SD = standard deviation.
Agroecology, Local Knowledge and Participatory Research
27
28 ETHNOBOTANY: Local Knowledge and Traditions
(Maytenus boaria), etc. Moreover, the results of the survey showed the presence
and/or use of species that had not been reported for this area but for other places
within the region studied by San Martín, such as linden (Tilia cf. europeae L.),
medlar (Eriobotrya japonica), culén (Psoralea glandulosa), plantain (Plantago
major), paico (Chenopodium ambrosioides), among others.
Other plants registered in the surveys, which San Martín (1983) mentioned for
medicinal uses but the surveyed population did not tie-in, were concli (Xanthium
spinosum) for stomach pain, the diuretic character of quinchamalí (Quinchamalium
majus), and the aphrodisiac properties of the herb of nail (Geum chiloense Bald),
inter alia. In a like manner, the surveys identified uses that were not reported
by San Martín, such as the properties attributed to cachanlahue (Centaurium
cachanlahuen), plantain (Plantago major) and avocado (Persea americana), to
name a few.
Of the species used by the locality, only 50% are available all through the year.
The remaining 50% are characterized by being seasonal products. Regarding this
particularity and based on the background obtained by the surveys, the community
established three categories: (a) those with permanent availability, (b) those with
marked seasonality and sporadic availability, and (c) those of seasonality and
permanent availability. From the first category (a), some herbs can be mentioned
such as pennyroyal (Mentha pulegium), mint (Mentha piperita), plantain (Plantago
major), and horizon (Tetraglochin alatum). With regard to those species defined as
marked seasonality and sporadic availability [second category (b)], other plants can
be named, e.g., cohile (Lardizabala bitermata), avocado (Persea americana), nalca
(Gunnera chilensis), medlar (Eriobotrya japonica), and prickly pear (Opuntia ficus-
indica), etc. Finally, for those species defined as seasonal and having a permanent
availability (category c), some plants can be included such as walnut (Junglans
regia), linden (Tilia cf. europaea L.), pile-pile (Modiola caroliniana), chamomile
(Matricaria chamomilla) and blackberry (Rubus ulmifolius). The condition of
permanent availability of this last group is due to how different peasant families
have developed multiple strategies that have allowed them to prolong the availability
of those resources that have a marked seasonality. One of these strategies has been
to apply/use various conservation techniques such as drying or the preparation of
preserves in the cases of leaves, and fruits, respectively. Other technique consists,
for example, in the application of some forced cultivation practices in the backyard
of the houses, which represents the prolongation of the forest ecosystem, also
contributing to the conservation of biodiversity. In this way, the products are
obtained out of season, which in no way implies the intensification of production,
since most of them are obtained from the collection and natural reproduction.
On the subject of the socialization of traditional knowledge, Fig. 2.2 clearly
shows that there was little exchange between families regarding the uses of non-
traditional products, since none of the reported species was known by all of the
families surveyed. In general, knowledge about the attributes and properties of
these species is exchanged (socialized) among family groups in which there is
some link or degree of friendship.
30 ETHNOBOTANY: Local Knowledge and Traditions
Grouping the species according to the number of families that knew its use, only
one of them—rue (Ruta graveolens)—turned out to be the species whose attributes
were known by the greatest number of families. On the other hand, a total of 26
species were only known individually by the families, but they were not necessarily
the same species for each family. Some examples of these species were pile-pile
(Modiola caroliniana), bailahuén (Haplopappus baylahuen), donkey tea (Viviania
marifolia), culén (Psoralea glandulosa), perlilla (Margyricarpus pinnatus), etc.
From the results, it was observed that of the all the families surveyed, there was
none who knew the use or properties of all the species registered.
The mechanism of assimilation and transfer of this knowledge is focused on
what is transmitted orally from generation to generation. This clearly shows that
the main socialization agency is the family, where the person from childhood is
able to know the forms of culture in which he/she was born.
was designed, including the selection of the relevant indicators, up to the evaluation
of the impact that such projects had on the quality of life and the sustainability of
their territories, among others.
In this way, it was possible to observe, from the developed experiences, the
relevance of the selection of indicators in a participatory mode (Peredo and Barrera
2016) because, fundamentally, these must exactly correspond (or fit) to concrete (or
specific) needs in a precise historical context, that is, the indicators are the “reflection
of the certain interests” of an evaluation in a “particular historical moment”. This
condition acquires greater relevance when the categories and ranges of valuation
have also been established in a participatory manner (Peredo et al. 2016) due to
the valuation exercises which achieve a sense of belonging to the community
through processes of permanent iteration in which the elements of subjectivity are
considered (Peredo and Barrera 2005).
As a final point, a special mention is made of the collective learning process
that was generated during these processes amongst the different actors, promoting a
real dialogue of knowledge. From the academic point of view, the multidisciplinary
integration carried out by professionals and undergraduates of diverse curricular
formations, who participated in research with rural communities, confirmed the
importance of dialogue between different perspectives, the cost of the reductionist
vision when dealing with complex phenomena (in terms of loss of diversity to
address the phenomenon), the inseparable relationship between theory and practice,
and the importance of a critical look at the modern perspective of development
(Peredo and Aedo 2016, Aedo et al. 2017).
Acknowledgements
The authors thank Dr. Amner Muñoz (Universidad del Norte, Colombia) for his
comments and reviews that improved the text, and to Vice Rectory of Research,
Development and Innovation (Universidad de Santiago de Chile) to support a stay
in the Agroecosystems History Lab (Universidad Pablo de Olavide, Sevilla-Spain).
References
Abarzúa, A., Donoso, P. and Donoso, C. 2007. Dasyphylum diacanthoides (Asteráceas). Trevo, tayo,
tevo, palo santo, palo blanco, Familia Asteraceae (Compositae). In: Donoso, C. (ed.). Las Especies
Arbóreas de los Bosques Templados de Chile y Argentina. Autoecología. Marisa Cueno Ediciones,
Valdivia, Chile.
Aedo, M.P., Peredo, S. and Schaeffer, C. 2017. From an essential being to an actor’s becoming: political
ecology transformational learning experiences in adult education. Environm. Educ. Res.
Altieri, M. and Nichols, C. 2000. Agroecología: teoría y práctica para una agricultura sustentable. Serie
Formación Ambiental Programa de la Naciones Unidas para el Medio Ambiente. PNUMA México.
Anrique, R., Molina, X., Alfaro, M. and Saldaña, R. 2014. Composición de alimentos para el ganado
bovino. Cuarta Edición. Universidad Austral de Chile-Inia, Valdivia, Chile.
Ardón, M. 2001. Métodos e instrumentos para la etnoecología participativa. Etnoecología 6: 129–143.
Ayala, A., Capetillo, C., Cetina, R., Sandoval, C. and Zapata, C. 2006. Composición química-nutricional
de árboles forrajeros. 1ªEd. Facultad de Medicina Veterinaria y Zootecnia, Universidad Autónoma
de Yucatán, Mérida, México.
32 ETHNOBOTANY: Local Knowledge and Traditions
Rodríguez, P., Fernández, M., Pacheco, J. and Cañal, M.J. 2005. Envejecimiento vegetal, una barrera a
la propagación. Alternativas. In: Sánchez-Olate, M.E. and Ríos-Leal, D.G. (eds.). Biotecnología
Vegetal en Especies Leñosas de Interés Forestal. Concepción, Chile.
San Martín, J. 1983. Medicinal plants in Central Chile. Econ. Bot. 37: 216–227.
Santelices, R. and Bobadilla, C. 1997. Arraigamiento de estacas de Quillaja saponaria Mol y Peumus
boldus Mol. Bosque 18: 77–85.
Santelices, R. and García, C. 2003. Efecto del ácido indolbutírico y la ubicación de la estaca en el
rebrote de tocón sobre la rizogénesis de Nothofagus alessandri Espinoza. Bosque 24: 53–61.
Santelices, R. 2005. Efecto del árbol madre sobre la rizogénesis de Nothofagus alessandri. Bosque
26: 133–136.
Taiz, L. and Zeiger, E. 1991. Plant physiology. The Benjamin/Cummings Publishing Company Inc.,
Los Angeles, California.
Toledo, V. 1993. La racionalidad ecológica de la producción campesina. In: Sevilla y González de
Molina (eds.). Ecología, campesinado e historia. La Piqueta, Madrid.
Toledo, V. and Barrera-Bassols, N. 2008. La memoria biocultural. La importancia ecológica de las
sabidurías tradicionales. Serie Perspectivas agroecológicas. Editorial Icaria, Barcelona, España.
Valencia, E. 2013. Validación y actualización del uso de plantas medicinales presentes en la selva
valdiviana. Tesis Químico Farmacéutico, Universidad Austral de Chile.
Van der Ploeg, J.D. 1990. Sistemas de conocimiento, metáfora y campo de interacción: el caso del
cultivo de la patata en el altiplano peruano. Agricultura y Sociedad 56: 143–166.
Zampini, I., Cudmani, N. and Isla, M.I. 2007. Actividad antimicrobiana de plantas medicinales argentinas
sobre bacterias antibiótico-resistentes. Acta Bioquim. Clin. Latinoam. 41: 385393.
Zea, J. and Díaz, M. 1990. Producción de carne con pastos forrajes. Centro de Investigaciones Agrarias
de Mabegondo. Xunta de Galicia, Santiago de Compostela, España.
CHAPTER 3
The Path of
Ethnopharmacobotany
From Economic Botany to Ethnobotany
Marcelo L. Wagner,* Leonardo M. Anconatani, Rafael A. Ricco,
Beatriz G. Varela and Gustavo C. Giberti †
Introduction
A transformation of knowledge is happening in the scientific field. There is a fresh
look where western science is not the only theoretical-practical model of assuming
reality. Other ways of knowing and perceiving nature are being raised. We started
studying how knowledge is passed on and has been passed on from generation to
generation, millenium to millenium, town to town, person to person. Therefore, other
kind of realities and other truths come together, prevail, are kept, are reproduced
and give rise to new knowledge, new perceptions, and cosmovisions about the
world, life, and nature.
This knowledge or “folk wisdoms” or “traditional knowledge” are the subject
of study of almost all scientific disciplines. Natural science is the most developed
area; fields like Ethnography, Ethnology, Antrophology, and Sociology have been
focusing on the study of the peoples and their associated knowledge. It is thus that
the prefix ethnos makes reference to human aspects and specific knowledge of the
peoples and ethnic groups, i.e., to the knowledge of groups of individuals of the
same culture (Arenas and Martínez 2013).
Nevertheless, we must bear in mind that human groups neither parcel nor
sectorize their knowledge, but have a general worldview, i.e., they do not have a
unidirectional view “the whole makes the part of the whole”. Therefore, they have
a holistic view of the world, they join past and future, lifeless with life, material
with spiritual, they link norms, values, nature, traditions, health, sickness, and
many other concepts with magic, legends, and myths that are an indissoluble part
of their knowledge and their daily practices (Arenas and Martínez 2013, Rengifo-
Salgado et al. 2017).
Let’s consider as premise that “traditional knowledge” is the practical
knowledge of ethnic groups or local communities which is based upon accumulated
and selected experience throughout thousands of years to obtain the best results in
the utilization of natural resources and their survival (Arenas and Martínez 2013).
As mentioned above, this knowledge must be grasped not only in a utilitarian
view, for example, when Botany investigates these sources of knowledge it
gives shape and sense to many of these concepts in Economic Botany, Medicine,
Agriculture, and Ecology, but we should take into account the worldview of the
community, who provided that knowledge. Thus, new fields of research are created,
such as Ethnobotany, Ethnomedicine, Agroecology, and Ethnoecology (Reyes
García and Martí Sanz 2007, Nolan and Turner 2011, Johnson and Davison-Hunt
2011).
At an early stage, information about medicinal flora, its usefulness, and ways
of usage were collected without considering the cultural setting in which that
knowledge was produced. Then, there was a progress towards a multidisciplinary
study, where humankind and the plants that they use to heal and the different
ways of usage were taken into account according to their worldview. We suggest
a journey through the history of different fields to disentangle the path towards
Ethnopharmacobotany and the importance of herbaria so that we can document
this ride.
Ethnoscience
Ethnoscience (or cognitive anthropology) is relatively young and it is placed on
the border of natural and social sciences. The term ethnoscience first appeared
in 1950, in the book Outline of Cultural Materials, where the author, George
Murdock, intended to make a thorough list of all the elements constituting human
culture. He subdivided this field of science in Ethnometeorology, Ethnophysics,
Ethnogeography, Ethnobotany, Ethnozoology, Ethnoanatomy, Ethnophysiology,
Ethnopsychology, and Ethnosociology (Murdock 1950). In this first stage, western
science is seen as superior with regard to cultures that were called “primitive”
back then. In such manner, he calls “exact sciences” to western knowledge while
he defines traditional knowledge as “non-systematized ideas about nature and
humankind” or “speculative and popular notions” (Beaucage 2000).
Stephen Tyler (1969) considered the ethnosciences as the study of the native
speech, not placing it within a western scientific order but to reinforce the ability that
36 ETHNOBOTANY: Local Knowledge and Traditions
Ethnobotany
Ethnobotany is the scientific study of the relationship between human groups
and their natural environment, whose name comes from the combination of two
fields of study: Ethnology (the study of culture) and Botany (the study of plants).
Researchers focus on the topic of this field from two perspectives. The first one
pursues a practical or utilitarian ideology and the second one is of philosophical
character. The most quoted definitions of this field are stressed in the research of
the relationship or interaction between humankind and the plant world (Jones 1941,
Ford and Jones 1978, Schultes and Von Reis 1995), in the impact that plants have
on human culture (Balick and Cox 1997), or a full record of the uses and concepts
of the plant kingdom in societies (Berlin 2014, Plotkin and Famolare 1992).
The term “Ethnobotany” was used for the first time in 1895 by John William
Harshberger, during his classes in the University of Pennsylvania (Harshberger
1895). However, the history of this academic field starts long before, since the
interest in Ethnobotany goes from the beginning of civilization, when human
beings perceived plants as a source of survival. Thus, the first men are practically
considered ethnobotanists, since they classified plants in different categories and
were capable of distinguishing those species that are beneficial from those which are
harmful (Choudhary et al. 2008). Teofrasto (c. 370–285 BC), the father of Botany,
The Path of Ethnopharmacobotany: From Economic Botany to Ethnobotany 37
describes the uses of economically important plants and sets the generic names
(for example: Crataegus, Daucus, and Asparagus) which are still being used. On
the other hand, Caius Plinius Secundus, better known as Plinio el Viejo, collected
information about the growth of medicinal plants in his work “Historia Natural”
(Bennet 2013). In the year 77, the Greek philosopher Dioscorides publishes the
work “De Materia Medica”, a record of around 600 plants of the Mediterranean
watershed that includes information related to the use (specially medicinal),
collection, toxicity, and edibility of such plants. Dioscorides also specifies the
economic potential of plants, anticipating in this way, the creation of Economic
Botany, interested in the use of plants which are useful to human beings and their
economic value (Wickens 2001).
The information of the classical age was repeated for over 1500 years. It was
only in the sixteenth century that European herbalists recorded new observations
about the use of plants. In 1542, a Renaissance artist, Leonhart Fuchs, listed 400
native plants from Germany and Austria in his book “De Historia Stirpium”,
followed by “Historia Plantarum” by John Ray, where the first definition of
“species” was published and subsequently, “Species Plantarum” by Carl Linnee,
which includes related information of about 5900 plants.
The collection of data about the use of plants was not only a European interest.
In the sixteenth century, Martín de la Cruz wrote the Aztec herbarium. His book,
known as “Manuscrito Badianus”, contains a description about the therapeutical
and psychoactive properties of 251 Mexican plants. This manuscript symbolizes
the first herbarium of medicinal plants written in the New World (Pease et al.
2000). Hipólito Ruiz López and José Antonio Pavón y Jiménez, Spanish botanists,
collected plant species in the viceroyalty of Peru and published them in “Flora
Peruviana et chilensis” (1798–1802). It is important to know that Chinese, Arab,
and Indian texts are produced in parallel, generally less known in the western
world, with valuable descriptions of the plant kingdom. However, the study of
this historical material is the subject of analysis of Historical Botany and not that
of Ethnobotany (Bennet 2013).
Linnee, whose latinized name represents the synonym of modern taxonomy,
was famous for the invention of the binomial method of nomenclature, where
the scientific name assigned to a species is made up by the combination of two
words (genus, species) (Loonen 2008). Linnee was also a pioneer of modern
Ethnobotany studies because he published “A tour in Lapland” where he made
detailed observations about the use of plants by the Sami peoples in Laponia
(Wickens 2001). Linnee’s successors did not limit their investigations to taxonomy,
for example, Alphonse de Candolle, wrote “Origen of cultivated plants” in 1885,
a classical work related to the origin of cultivated plants.
The Summit of botanical exploration took place in the eighteenth and nineteenth
century. It is worth mentioning the trips of Alexander von Humboldt and Aimé
Bonpland, and James Cook. On the other hand, the English botanist Richard
Spruce, one of the great Victorian botanist explorers, took 15 years to explore
the Amazon (mainly all Brazil). His collections, indexed in the Royal Botanical
38 ETHNOBOTANY: Local Knowledge and Traditions
Fig. 3.1. Cover of the Spanish version of the book “Natural History” of Cayo Plinio (1624).
Fig. 3.2. Cover of the Speech by Pierre Andrea Matthioli on the work of Dioscoride (1568).
“native botany” (which is devoted to the research of those types of plants used
by natives aimed, among others, to the obtention of food, medicine, and fabrics)
(Fig. 3.4). The term “native botanical” was used for the first time in 1874 by
Stephen Powers. An essential part of study in this field is called “folk” or popular
taxonomy, referring to the method used to ease the recognition and designation of
plants used by members of a certain linguistic community (Sánchez et al. 2007,
Berlin 2014). Sometimes, native nomenclature tells a lot about the characteristics of
the plant, vegetation, or its effects (if it is toxic or nutritious, or laxative, astringent,
sedative, or without any active ingredient) (Powel 1877). A publication of Leopold
Glueck, a German physician who worked in Sarajevo, which is about traditional
medicine and the plants used by rural population in Bosnia from an emic point of
view (created from phonemes), is considered to be the first modern ethnobotanical
40 ETHNOBOTANY: Local Knowledge and Traditions
work (Cunningham 2001). “Emic” and “ethic” are technical terms originally derived
from the suffixes of the words ‘phonemic’ and ‘phonetic’ suggested by the linguist
Kenneth Pike in 1967. The first term relates to any unit of sound in a particular
language and the second, to the system of notations cross-culturally useful which
those “vowel sounds” represent (McCutcheon 1999).
At the beginning of the twentieth century, the neologism by Harsberger
“Ethnobotany” is approved, although it is only about a semantic replacement.
The change of paradigm that gave rise to a more conceptual and methodological
The Path of Ethnopharmacobotany: From Economic Botany to Ethnobotany 41
in which they are. Later, the Ethnobotany becomes a cultural topic and currently,
scientists are trying to understand it from this perspective. Lastly, the scope of
this field redefines “humankind” and creates a new concept. At present, the term
“traditional” is used since it is less derogatory than the one used before, that is,
“primitive” (Ford and Jones 1978, Cotton 1996).
An important point is to know if there is a key difference between the traditional
and modern use and handling of plants. This distinction can be artificial, since
etymologically, there is no reason to restrict Ethnobotany from traditional societies.
The prefix “ethno” refers to any people or cultural group, not only traditional
societies (Rodríguez-Echeverry 2010, Bennet 2013).
The current frame of Ethnobotany emphasizes the different skills needed by the
scientists of this field: a necessary botanical background to identify and preserve
plant samples, an anthropological training that helps the researcher understand
cultural concepts, and a linguistic background that allows the researcher to be able
to transcribe terms and understand the morphology, syntax, and native semantics
(Choudhary et al. 2008). The investigation of the practical functions of plants
dominates the research agenda. The Ethnobotany, as discipline, is oriented to the
exploration of new plant resources, the collection of genetic material, the discovery
of drugs or medicines resulting from plants, and the development of new natural
products (Plotkin et al. 1992, Schultes and Von Reis 1995, Balick and Cox 1997).
Ethnopharmacology
The term Ethnopharmacology was used for the first time by Efron et al. (1967).
It was implemented in the title of the book Ethnopharmacological Search for
Psychoactive Drugs, which deals with the ethnopharmacological search of
psychoactive drugs (Efron et al. 1970, Holmstedt 1967).
Ethnopharmacology is, by definition, a scientific approach to the study of the
biological activities of any preparation used by human beings traditionally, which
have in a broad sense, beneficial, toxic or other pharmacological direct effects. As
such, we do not attempt to describe uses (generally local or traditional) but some
characteristics about the large antrophological and pharmaco-toxicological study
of these preparations.
Furthermore, studies that describe the medicinal use of plants are generally
included in this definition, but these studies are performed with the aim of leading
to an experimental investigation of medicinal plants, in other words, validating the
use that one human group gives to plants (Heinrich et al. 2009).
The study of traditional drugs by ethnopharmacologists does not have the
purpose to advocate for a return to the use of these remedies as used by communities,
nor to promote traditional medicine. The objective is, thus, to rescue and document
a cultural heritage before it gets lost to be able to investigate and evaluate it.
Therefore, Ethnopharmacology involves a multidisciplinary work in which
botanists, phytochemists, and pharmacologists are found, and where anthropologists
have an active participation. The first investigation with this multidisciplinary
The Path of Ethnopharmacobotany: From Economic Botany to Ethnobotany 43
Fig. 3.6. Herbarium of Pharmacobotany Museum “Juan Aníbal Domínguez”, Buenos Aires,
Argentina.
The Path of Ethnopharmacobotany: From Economic Botany to Ethnobotany 45
housed in great herbaria are plants of useful or symbolic value to human beings. An
interesting work would be an ethnopharmaceutical investigation of the botanical
collections of herbaria placed in museums or academic institutions (Bebber et al.
2010, Nesbitt 2014).
During the twentieth century, herbaria were driven away from their roots since
they went from collections of useful plants to be the material used by taxonomists
for alpha taxonomy, detection, description, and classification of taxa. Researchers
lost their interest in human interaction with plants (Anderson 1952). Perhaps, this
was not by chance. Towards the end of the twentieth century, a crisis in the botanical
collections was recorded which gave rise to a decrease of funding and a lack of
confidence in the value of the collections of the museums (Clifford et al. 1990).
At present, opinion has changed since there is, as mentioned before, an
important source of information which revalues the importance of herbaria (Funk
2003, Suarez and Tsutsui 2004).
It is important to keep in mind that herbarium samples fulfil three vital functions:
they allow the identification of the specimen botanically, they allow identifications
to be controlled by other researchers, and they allow updating the work in the light
of new taxonomical concepts. Why are these functions so important?
Most of the plants that are found in the ethnobiological field of work, certainly,
already have an identification in the form of a local vernacular name. As far as
preservation of traditional knowledge and record of ethnotaxa goes, vernacular
names are essential. However, the identification of a species by botanical name
(latin) is also essential since it allows to have a comprehensive knowledge of the
plant, for example, the uses that it might have in other cultures, phytochemical,
pharmacological, ecological studies, and plant growing (Bennett and Balick 2013).
Botanical names are also, in theory, less bound to ambiguity than vernacular names;
they can often be written in different ways when they are registered and the same
name can be used for more than one species (Bennet and Balick 2013). On the
other hand, the identification of a plant requires that the material contains flowers
or fruits to use the standard botanical tools such as the flora or the comparison with
samples of reference herbaria, that are often missing in the ethnopharmacological
specimens, such as the plant drug formed by some of the vegetative organs of the
plant or exudates (Eisenman et al. 2012). In many cases, the identification is made
in the field, for which handbooks or the botanical expertise of the researcher are
used, but there is a risk of confusing the well-known species with new species
that have a similar aspect. Field identifications are uncertain and it is necessary to
confirm them with morphological studies in the laboratory, and many times it is
necessary to resort to chemical studies or to DNA molecular biology to confirm
them (Eisenman et al. 2012).
In genetics, herbarium samples have allowed the reinterpretation of results
of hybridization experiments decades after they had occurred, in light of new
taxonomical arrangements (Sauer 1953, Barkworth and Jacobs 2001). Likewise,
the new taxonomical work of Schmidt-Lebuhn (2008) about the aromatic gender
46 ETHNOBOTANY: Local Knowledge and Traditions
Conclusion
Traditional medicine, just like folk medicine, is a system of practices and own
remedies proper of native societies, even if in certain cases and for geographical
reasons it is possible to isolate their components. Traditional medicine as well
as folk medicine contain an indeterminate number of followers and mostly
non-explicitly written rules. In general, the historical information known comes
from secondary testimonies.
The limits among the three medical systems (scientific, traditional, and folk)
are not very clear, though. Clarity is blurred inasmuch as their study is deepened,
contacts and conceptual confluences appearing as a consequence. Adoption and use
of different remedies and medical practices encourage to reflect on the similarities
and not only on differences and contrasts.
It is necessary to keep in mind that the three great medical groups–scientific
medicine, folk medicine, and traditional medicine—share a common characteristic:
rational thinking. This is not a privilege of western societies but it is also observed
in different contexts. Lévi-Strauss expressed that conceptual proliferation is not an
exclusive heritage of the “civilized” but that the “primitive” thinking also introduces
abstract and complex elements, led by an interest in classifying and organizing
the environment. In other words, there is a systematically developed knowledge
among the people we call “primitive”, even without a practical utility, i.e., it is
not related to vital needs, such as food or medicine, but with previous intellectual
requirements. The will to introduce an order, a taxonomy, is a common point with
modern science and it is found in the basis of all human thought (Di Liscia 2003).
The Path of Ethnopharmacobotany: From Economic Botany to Ethnobotany 47
References
Anderson, E. 1952. Plants, Man and Life. Little, Brown and Company, Boston.
Arenas, P. and Martínez, G.J. 2013. Estudio etnobotánico en Regiones Áridas y Semiáridas de Argentina
y zonas limítrofes. Experiencias y reflexiones metodológicas de un grupo de investigación.
pp. 11–43. In: Arenas, P. (ed.). Etnobotánica en Zonas Áridas y Semiáridas del Conosur de
Sudamérica., CONICET, Buenos Aires.
Balick, M.J. and Cox, P.A. 1997. Plants, People, and Culture: The Science of Ethnobotany. New York,
EEUU: Scientific American Library.
Beaucage, P. 2000. La etnociencia, su desarrollo y sus problemas actuales. Cronos 3(1): 47–92.
Bebber, D.P., Carine, M.A., Wood, J.R.I., Wortley, A.H., Harris, D.J., Prance, G.T., Davidse, G., Paige,
J., Pennington, T.D., Robson, N.K.B. and Scotland, R.W. 2010. Herbaria are a major frontier for
species discovery. PNAS 107(51): 22169–22171.
Bell, S. 2010. A Life in Shadow. Aimé Bonpland in Southern South America, 1817–1858. Stanford
University Press.
Bennet, B.C. 2013. Economic botany—Ethnobotany and economic botany: Subjects in search of
definitions. In: Encyclopedia of Life Support Systems. (EOLSS). Paris, Francia: EOLSS Publishers.
Bennett, B.C. and Balick, M.J. 2013. Does the name really matter? The importance of botanical
nomenclature and plant taxonomy in biomedical research. J. Ethnopharmocol. 152(3): 387–392.
Berlin, B. 2014. Ethnobiological classification: principles of categorization of plants and animals in
traditional societies. Princeton, New Jersey: Princeton University Press.
Clifford, H.T., Rogers, R.W. and Dettmann, M.E. 1990. Where now for taxonomy? Nature 346: 602.
Cotton, C.M. 1996. Ethnobotany: Principles and applications. Chichester, West Sussex, UK: Wiley.
Cristofolini, G., Mossetti, U. and Bonfiglioli, C. 1993. Pre-Linnean herbaria in Bologna: some newly
discovered collectors from time of Ulisses Aldavani. Webbia 48: 555–565.
Cunningham, A.B. 2001. Applied ethnobotany: People, wild plant use and conservation. London, UK:
Earthscan Publishing Limited.
de Candolle, A. 1885. Origin of cultivated plants. Nueva York, EEUU: D. Appleton.
Choudhary, K., Singh, M. and Pillai, U. 2008. Ethnobotanical survey of Rajasthan—An update. AEJB
1(2): 38–45.
EFSA. 2011. Scientific opinion on pyrrolizidine alkaloids in food and feed. EFSA Journal 9(11): 1–134.
Eichele, K. 2010. Phytotherapy—An introduction. The Journal of the European Medical Writers
Association 19(1): 67.
Eisenman, S.W., Tucker, A.O. and Struwe, L. 2012. Voucher specimens are essential for documenting
source material used in medicinal plant investigations. Journal of Medicinally Active Plants 1: 8.
Fertig, W. 2016. Are Herbaria Still relevant in the 21st Century? https://biokic.asu.edu/blog/are-herbaria-
still-relevant-21st-century (September 2017).
Ford, R.I. and Jones, V.H. 1978. The nature and status of ethnobotany. Ann Arbor, MI: Museum of
Anthropology, University of Michigan.
Fresquet Febrer, J.L. 1994. Guía para la realización de trabajos de folkmedicina y otros sistemas
médicos. Cuadernos Valencianos de Historia de la Medicina y de la Ciencia. Seria A (monografías).
48 ETHNOBOTANY: Local Knowledge and Traditions
Sequeira, L. 2006. Richard Evans Schultes: January 12, 1915–April 10, 2001 (A Biographical memoir).
Washington, D. C., USA: National Academy Press.
Shirwaikar, A., Verma, R. and Lobo, R. 2009. Phytotherapy—Safety aspects. Nat. Prod. Rad. 8(1): 55–63.
Schultes, R.E. and Von Reis, S. 1995. Ethnobotany: Evolution of a discipline. New York, USA:
Dioscorides Press.
Stafleu, F.A. and Cowan, R.S. 1976–1988. Taxonomic Literature (2º edition) Vol. 1-7. Regnum Vegetabile
94, 98, 105, 110, 112, 115, 116. Bohn, Scheltema & Holkema, Utrecht.
Suarez, A.V. and Tsutsui, N.D. 2004. The value of museum collections for research and society.
BioScience 54: 66–74.
Thoreau, H.D. 1906. Walden. La vida en los bosques. http://consumoetico.webs.uvigo.es/textos/
walden.pdf.
Thoreau, H.D. 1906. The writings of Henry David Thoreau (B. Torrey, Ed.). Boston, New York:
Houghton, Mifflin and Company.
Tyler, S. 1969. Cognitive Anthropology. New York, Holt, Rinehart, and Winston.
Wickens, G.E. 2001. Economic Botany. Principles and Practices. Kluwer Academic Publishers.
CHAPTER 4
Patagonian Berries
An Ethnobotanical Approach to Exploration of
their Nutraceutical Potential
Melina F. Chamorro,1 Ana Ladio1,* and Soledad Molares2
Introduction
Inhabitants of rural communities in Argentine-Chilean Patagonia are mainly
of Mapuche-Tehuelche origin, while others have Creole ancestry and/or are
descendants of different waves of settlers who arrived in the región more than a
century ago (Ladio and Molares 2014). The vast Patagonian territory is characterised
by its great environmental diversity, including mountainous regions, steppe, forests
and ecotones, which have provided inhabitants with subsistence resources since
ancient times (Vignati 1941, Nacuzzi and Perez de Micou 1984, Prattes 2009,
Llano and Barberena 2013). Even today, despite the marked increase experienced
in urbanisation and markets, inhabitants of rural Patagonia continue to make use of
the different ecological environments, and have therefore accumulated extensive
knowledge of their plant surroundings (Ladio and Lozada 2001, 2008, Richeri et
al. 2013). The close relationship they have established with plants is particularly
evident when considering the species used by local families to treat illness and
provide food (Ladio 2001, Ladio and Lozada 2004, Ladio 2005, Molares and Ladio
2009b, Ochoa and Ladio 2015).
Native fruits have been much used by local populations as part of their diet,
according to archaeological and recent records (Martínez-Crovetto 1982, Dillehay
1
INIBIOMA.Quintral 1250-S.C. de Bariloche, Río Negro, Argentina.
2
CIEMEP, CONICET-Universidad Nacional de la Patagonia San Juan Bosco. Roca 780, Esquel (9200),
Chubut, Argentina.
* Corresponding author: [email protected]
Patagonian Berries 51
1988, Rapoport and Ladio 1999). In this work, we are particularly interested in
the berries which are native to this región. Pochettino (2015) proposed that berries
correspond principally to the fleshy fruits of trees and shrubs of temperate areas,
generally red to violet in colour, and are also called “soft fruits”. In their natural
state they normally contain more than 50% water, which they contribute to the
people’s diet, and are low in calorific value. The sugars they contain are easily
digested and absorbed by the body, and they also enrich the diet with fibre, minerals
and vitamins (Hurrell et al. 2010). Berries can be classified generally into simple
fruits, with pips (pome fruit), stones (drupes and polydrupes) and aggregate fruits
(thickened receptacles containing partial fruits).
Most of the best known species throughout the world were domesticated a
long time ago, and have become valued resources in the international and the local
market for Argentina and Chile: strawberry (Fragaria x ananassa), raspberry (Rubus
idaeus), highbush blueberry (Vaccinium corymbosum) and cherry (Prunus avium),
among others (Hurrell et al. 2010). In Northwestern Patagonia, there is a sizeable
market for food products based on exotic berries, which provides work for the local
population and also migrant workers who come from other localities to work on the
cultivation and harvesting of the soft fruit (Ladio et al. 2013). However, there are
also numerous wild or semi domesticated “berries” which have been little studied,
as in the case of the native Patagonian species.
In addition to their attraction as edible fruits, berries have become recognised
on a global level as conferring health benefits, which has led to research on their
bioactive compounds (Szajdek and Borowska 2008). Epidemiological evidence
demonstrates that certain plant compounds are related to effects that protect against
the development of cancer, cardiovascular disease, diabetes, osteoporosis and
neurodegenerative illnesses (Pandey and Rizvi 2009). New concepts arise from the
perspective that considers there to be a strong link between diet and health, such as
functional foods and nutraceuticals. Functional foods are those which, in addition to
their nutritional properties, also contribute to the prevention of disease. The name
“nutraceutical” is generally given to a product that takes on a pharmaceutical form
(e.g., capsules, pills, granules), whose production is based on a food substance, or
part of one (Mahabir 2014). In this text, we use “nutraceutical potential” to refer
to any foodstuff that may provide the dual benefit of nutrition and health.
On studying the reasons behind many of the beneficial effects of diets rich
in fruit and vegetables, it was found that their antioxidant properties were mainly
responsible for providing these benefits (Szajdek and Borowska 2008). An
antioxidant substance has a high capacity for absorption of free radicals, even at a
low concentration. These are radical oxygen and nitrogen species, highly reactive
molecules which can damage different cell components (Shahidi and Naczk
2004). In our diet we can find natural antioxidants made up mainly of phenolic
and polyphenolic compounds, such as anthocyanins, phenolic acids, flavonoids,
stilbenes and tannins, all from plants (Shahidi and Naczk 2004).
In general, uptil now, the most studied berry species have been from the
northern hemisphere, due to their high levels of natural antioxidant, specifically
52 ETHNOBOTANY: Local Knowledge and Traditions
geographical distribution of the species were corroborated using Flora del cono
sur (Zuloaga and Morrone 2009), and only species occurring in Argentine-Chilean
Patagonia were included.
Species with records of only edible and/or edible and medicinal uses in their
sources of origin were selected, excluding the records which mentioned only
medicinal use. This criterion was based on the likelihood that the overlapping of
alimentary and medicinal uses would reveal those species with high nutraceutical
potential (Ladio 2011). We recorded a species as edible when the source referred
to the use as food, drink with or without alcohol, sweets, jams, or the consumption
of fresh or dried fruit (Ladio 2005). The use was recorded as medicinal when the
literature indicated that it was considered capable of curing an illness, relieving
pain, or treating or counteracting a symptom of any kind (Estomba et al. 2006,
Molares and Ladio 2009a). Unfortunately, in the records the medicinal property
is often associated with a species, and details as to which part of the plant is used
do not always figure.
Potentilla chiloensis frutilla silvestre, Rosaceae ARG (Neuquén, Río Negro)/CHL (VI, VII, VIII, IX, f perennial conocarp 33
(L.) Mabb. llahuén, wild X, XI, IJF) plant
strawberry
Ribes magellanicum parrilla, Grossulariaceae Variety magellanicum ARG (Río Negro, Santa Cruz, f, sc shrub berry 33
Poir. zarzaparrilla, mulul, Tierra Del Fuego)/CHL (VI, VII, VIII, IX, X, XI, XII,
magellanic currant metropolitan)
Berberis darwinii michay, calafate, Berberidaceae ARG (Chubut, Neuquén, Río Negro, Tierra del f, sc shrub berry 29
Hook. darwin’s barberry Fuego)/CHL (VII, VIII, IX, X, XI)
Gaultheria mucronata chaura, prickly heath Ericaceae ARG (Chubut, Neuquén, Río Negro, Santa Cruz, f shrub berry 25
(L.f.) Hook. & Arn. Tierra del Fuego)/CHL (VIII, IX, X, XI, XII)
Empetrum rubrum Vahl mutilla, red Empetraceae ARG (Chubut, Mendoza, Neuquén, Río Negro, Santa f, sc, pb, s shrub drupe 24
ex Willd. crowberry Cruz, Tierra del Fuego)/CHL (V, VII, VIII, IX, X, XI,
XII, metropolitan, Juan Fernández archipelago)
Amomyrtus luma luma, palo madroño Myrtaceae ARG (Chubut, Neuquén, Río Negro)/CHL (VII, VIII, f shrub or berry 22
(Molina) Legrand et IX, X, XI) tree
Kausel
Ugni molinae Turcz. murta, ugni, chilean Myrtaceae ARG (Chubut, Neuquén, Río Negro)/CHL (V, VI, f shrub berry 22
guava, strawberry VII, VIII, IX, X, XI, XII)
myrtle
Luma apiculata (DC.) arrayán, palo Myrtaceae ARG (Chubut, Neuquén, Río Negro)/CHL (IV, V, VI, f shrub or berry 19
Burret colorado, VII, VIII, IX, X, XI, metropolitan) tree
chilean myrtle
56 ETHNOBOTANY: Local Knowledge and Traditions
Fig. 4.1. General appearance of the 10 most frequently cited berries’ species in order of use consensus.
1. Berberis microphylla, 2. Aristotelia chilensis, 3. Potentilla chiloensis, 4. Ribes magellanicum var.
magellanicum, 5. Berberis darwinii, 6. Gaultheria mucronata, 7. Empetrum rubrum, 8. Amomyrtus
luma, 9. Ugni molinae, 10. Luma apiculata.
Photographic Credits
1. Melina F. Chamorro; 2. Melina F. Chamorro; 3. Melina F. Chamorro; 4. Ana H. Ladio; 5. Melina
F. Chamorro; 6. Ana H. Ladio; 7. Ana H. Ladio; 8. Melina F. Chamorro; 9. Melina F. Chamorro;
10. Ana H. Ladio
also prepared a drink with the fruit of this species, but in contrast to chicha, it is not
fermented. The use of B. microphylla for medicinal purposes has been described
in the Mapuche medical system as being refreshing for feverishness and useful for
treating indigestion (Gusinde 1917, Mösbach 1992). Mösbach (1992) also refers
to use of the fruit for treating diarrhea.
In modern times, gathering practices still persist in the Mapuche communities
of Neuquén, Río Negro and Chubut (Ladio and Rapoport 1999, Ladio 2001, Ladio
and Lozada 2004, Ladio 2006, Lozada et al. 2006). The fruit is collected despite
the great distances locals have to cover to find the plants, as in the case of the Rams
Mapuche community, from Paraje de la Media Luna (Neuquén province). The
gathering method these communities use is of particular interest, as it helps them
avoid being pricked by the plant’s spines. In their walks into the countryside, the
women and children carry a recipient and a stick or branch with which to hit the
Patagonian Berries 57
bush so that the mature fruit falls to the ground. Although the small children prefer
to eat the fruit raw, in general it is used to make jellies, jams, and juices (Ladio
2001, Rapoport et al. 2005). For medicinal purposes, the fruit of B. microphylla is
used as a febrifuge, for example, in the Curruhuinca Mapuche community in San
Martin de los Andes (Conticello 1997).
It was also found that they possess a higher content of anthocyanins and a higher
antioxidant capacity than 10 other Chilean berry species (Ruiz et al. 2013). When
comparing calafate berries with five berries (including Ugni molinae and Luma
apiculata), they not only had higher levels of phenolic compounds, but also had
the highest antioxidant capacity (Ramirez et al. 2015). In the same study, calafate
fruits, were also highlighted in one trial in which the inhibition of peroxidation of
human erythrocytes was evaluated (Ramirez et al. 2015).
to the production of jams, liqueurs, and even maqui coffee are increasing. These
products are all prepared with fruit that comes directly from the gathering practices
of wild populations, and therefore sustainable forms of management and cultivation
are being sought.
The antioxidant capacity of A. chiloensis is principally attributed to its high
content of anthocyanins, and these have been studied in Chile for some time now
(Escribano-Bailón et al. 2006). In order to identify genotypes that will prove suitable
for cultivation, in recent years studies have focused on finding the fruit with the best
anthocyanin profile (Fredes et al. 2014). On the other hand, many pharmacological
properties are being investigated, among which its antidibetogenic and analgesic
effects seems to be outstanding (Romanucci et al. 2016).
The wild strawberry was studied in terms of its phenolic compounds and
antioxidant activity of the fruit, leaf and rhizomes (Simirgotis and Schmeda-
Hirschmann 2010, Schmeda-Hirschmannn and Simirgiotis 2011), as well as the
different parts of the fruit (Cheel et al. 2007). In addition, Avila et al. (2017) have
verified the protective activity of extracts of Potentilla chiloensis f chiloensis in
gastric cells exposed to free radicals and proposed the prevalent mechanism of
cytoprotection.
nam peoples. Its use is well documented in the preparation of drinks, including
chicha, in the Mapuche communities that lived in Argentine-Chilean Patagonia
(Mösbach 1992). Gusinde (1917) recorded the refreshing and febrifuge qualities
of these berries, and the same properties have been cited for the leaves (Houghton
and Manby 1985).
Several more recent studies (Lozada et al. 2006, Eyssartier 2011a,b) reveal
that the fruit is consumed in different rural populations of Argentina. This use
is also referred to on the island of Chiloé by Contreras Vega (2007), who also
mentions the febrifuge properties of its fruit, leaves and roots. B. darwinii has
been studied for its alkaloid content (Srivastava et al. 2015). This species has a
similar antioxidant profile to B. microphylla flavonols, a fact that provides some
suggestions for future research.
1969–1999). The plants flower at the end of the winter and bear fruit in spring and
early summer.
According to various sources (Ragonese and Martínez-Crovetto 1947,
Martínez-Crovetto 1982, Mösbach 1992), the fruit has an acid flavour and has been
eaten raw in the past by Mapuche, Alacalauf, Selk-nam and Yaganes communities.
The berries were considered refreshing and good for the stomach (Mösbach 1992).
Data obtained from current studies, for example in the Paineo Mapuche
community and the rural Creole community of Cuyín Manzano in Neuquén
province, have shown persistence in its use as a food resource, but not in its
medicinal use (Ladio and Lozada 2004, Lozada et al. 2006).
In this review, phytochemical studies on E. rubrum with regard to antioxidant
substances have not been found.
reach 0.5 g, so that a large bush can produce 1 kg of these berries (Rapoport et al.
2003). The fruit is produced mid summer, and is sweet and aromatic.
According to Gusinde (1917), the Mapuche made wine with the fruit, as well
as chicha and jams, or the berries were eaten fresh or dried (Muñoz et al. 1981,
Mösbach 1992). Tonic, stimulant and astringent properties were attributed to the
beverages prepared (Muñoz et al. 1981, Mösbach 1992).
At present, U. molinae stands out as one of the non-woody forest product,
mostly commercialised as a food resource in the IX region of Chile (3278 kg/year in
the Valdivian region) (Tacón et al. 2006). From a medicinal point of view, although
still mentioned in current bibliography (Pardo and Pizarro 2005), its use has not
been confirmed. In craft fairs and/or street markets in the south of Chile, jams,
liqueurs and murta in syrup can be obtained. In Argentina, its commercialisation
as a food resource has not been recorded.
The anthocyanin and antioxidant profile of this species has been studied, and it
was found to have a simple pattern with only six anthocyanins. Nevertheless, this
species has a strong activity in inhibition of lipid peroxidation in human erythrocytes
and scavenging of superoxide anion tests (Ramírez et al. 2016).
about plants. Rural children learn to gather them when they are small, especially if
their parents continue to follow the pastoral lifestyle. This is possibly due, in part,
to their visibility compared to the other eight berries highlighted in this review, an
aspect which should be studied in greater detail.
In general, we could say that these berries could be considered prototypical:
they are globose, red-bordeaux, shiny, spineless, turgid, etc., they have everything
that would be expected from an edible fruit—“they are tasty and they are not bad
for you”—according to local inhabitants. In this sense, these species are easy to
identify, to harvest, and they are not confused with toxic plants, which means
that children can easily gather them. In general, their sweet, delicate flavours are
considered inoffensive, suitable for consumption by children according to the
criteria of the rural inhabitants we have worked with (Molares and Ladio 2009b).
“It’s sweet, so we can eat it”, mentioned various informants. If, on the other hand,
the berries were tasteless, or bitter, the people would be in doubt.
Our interpretation is that they are elements with a certain duality, being used
in both alimentary and health contexts. Various case studies show that from a
local perspective, health and diet are intimitely linked (Ladio 2011). For example,
ethnobotanical studies carried out in Mapuche communities reveal a marked overlap
between edible and medicinal species (Ladio 2006, Molares and Ladio 2015).
This duality forms part of a traditional health system based on varied cultural
contributions, the best known and the most widespread in the region being the
Mapuche traditional health system, which has become hybridised with elements
from Creole and other cultural heritages (Citarela et al. 1995, Molares and Ladio
2009b). Significantly, this view of integrality in traditional systems now has its
equivalent in scientific environment within the subject of functional foods.
The long period of time over which sources cite their use reveals the cultural
importance of these ten species that persists in the societies, even though there have
been slight differences and changes over time. Although the original communities
in the region have given new meanings to their alimentary and health systems over
time, mainly due to the imposition of strong measures following the conquest and
national politics, these species continue to be used and appreciated in the lives of
rural workers.
Their use does not appear to have been affected by the drastic introduction of
new foods or the notorious change in landscapes these people underwent (Eyssartier
et al. 2011b, Torrejón and Cisternas 2002). Many traditional practices have
withstood the hybridisation processes of traditional wisdom with new knowledge
that came from European immigrants or from the societies that emerged after the
formation of the Argentine and Chilean states. Furthermore, some species, such
as maqui, are taking on even more importance on a commercial and global scale.
Finally, this list is intended to give an overview of the principal fruits consumed
by the first inhabitants of this part of South America, and up to the present time.
From an ethnobotanical point of view, further research is necessary, in particular
on the subject of traditional managment practices these species are subject to,
the social rules relating to extraction and conservation, and the conservation
Patagonian Berries 65
Acknowledgements
We would like to thank the men and women from the different Argentine Patagonian
communities (especially Cuyín Manzano, and the Mapuche communities of Catán
Lil, Lago Rosario and Nahuelpan) for their friendly conversation and the affection
shown to us during our work. Our thanks also go to CONICET. This investigation
has been financed by PIP 2013-0466 held by Phd. Ana Ladio.
References
Arena, M.E. and Curvetto, N. 2008. Berberis buxifolia fruiting: Kinetic growth behavior and evolution
of chemical properties during the fruiting period and different growing seasons. Sci. Hortic.
118: 120–127.
Arena, M.E. and Coronel, L.J. 2011. Fruit growth and chemical properties of Ribes magellanicum
“parrilla.” Sci. Hortic. 127: 325–329.
Arena, M.E., Giordani, E. and Radice, S. 2014. Flowering, fruiting and leaf and seed variability in
berberis buxifolia, a native patagonian fruit species. pp. 1–20. In: Marin, L. and Kovac, D. (eds.).
Native Species: Identification, Conservation and Restoration. Nova Science, New York, USA.
Ávila, F., Theoduloz, C., López-Alarcón, C., Dorta, E. and Schmeda-Hirschmann, G. 2017.
Cytoprotective mechanisms mediated by polyphenols from chilean native berries against free
radical-induced damage on AGS cells. Oxid. Med. Cell. Longev. 2017: 1–13.
Capparelli, A., Hilgert, N. and Ladio, A. 2011. Paisajes culturales de Argentina: Pasado y presente
desde las perspectivas etnobotánica y paleoetnobotánica. Argent. Ecol. Paisajes. 2(2): 67–79.
Cheel, J., Theoduloz, C., Rodríguez, J.A., Caligari, P.D.S. and Schmeda-Hirschmann, G. 2007. Free
radical scavenging activity and phenolic content in achenes and thalamus from Fragaria chiloensis
ssp. chiloensis, F. vesca and F. x ananassa cv. Chandler. Food Chem. 102: 36–44.
Citarella, L., Conejeros, A.M., Espinosa, B., Jelves, I., Oyarce, A.M. and Vidal, A. 1995. Medicinas y
culturas en La Araucanía. Ed. Sudamericana, Santiago, Chile.
66 ETHNOBOTANY: Local Knowledge and Traditions
Conticello, L., Gandulo, R., Bustamante, A. and Tartarglia, C. 1997. El uso de plantas medicinales
por la comunidad mapuche de San Martín de los Andes. Provincia de Neuquén (Argentina).
Parodiana. 10(1-2): 165–180.
Contreras Vega, M. 2006. Plantas medicinales y alimenticias de Chiloe. Colección Cultura Insular.
Castro, Chile.
Correa, M.N. (ed.). 1969–1999. Flora Patagónica 8, Partes 1–7. Col. Ci. INTA, Buenos Aires, Argentina.
Damascos, M.A. 2011. Arbustos silvestres con frutos carnosos de Patagonia. Fondo Editorial Rionegrino,
Viedma, Argentina.
Davidson-Hunt, I.J. and Berkes, F. 2003. Nature and society through the lens of resilience: toward
a human-in-ecosystem perspective. In: Berkes, F., Colding, J. and Folke, C. (eds.). Navigating
Social-Ecological Systems: Building Resilience for Complexity and Change. Cambridge University
Press, Cambridge, UK.
Dillehay, T.D. 1988. Monte Verde: a Pleistocene settlement in Chile. Vol I. Paleoenvironment and site
context, Smithsonian Institution Press, Washington DC, USA.
Escribano-Bailón, M.T., Alcalde-Eon, C., Muñoz, O., Rivas-Gonzalo, J.C. and Santos-Buelga, C.
2006. Anthocyanins in berries of Maqui (Aristotelia chilensis (Mol.) Stuntz). Phytochem Anal.
17(1): 8–14.
Estomba, D., Ladio, A. and Lozada, M. 2006. Medicinal wild plant knowledge and gathering patterns
in a Mapuche community from North-western Patagonia. J. Ethnopharmacol. 103(1): 109–119.
Eyssartier, C., Ladio, A.H. and Lozada, M. 2011a. Traditional horticultural knowledge change in a rural
population of the Patagonian steppe. J. Arid. Environ. 75(1): 78–86.
Eyssartier, C., Ladio, A.H. and Lozada, M. 2011b. Horticultural and gathering practices complement each
other: a case study in a rural population of northwestern Patagonia. Ecol. Food Nutr. 50: 429–451.
Falkenberg, S.S., Tarnow, I., Guzman, A., Mølgaard, P. and Simonsen, H.T. 2012. Mapuche herbal
medicine inhibits blood platelet aggregation. Evidence-based Complement. Altern. Med. 1–9.
Fredes C., Yousef, G.G., Robert, P., Grace, M.H., Lila, M.A., Gómez, M. and Montenegro, G. 2014.
Anthocyanin profiling of wild maqui berries (Aristotelia chilensis [Mol.] Stuntz) from different
geographical regions in Chile. J. Sci. Food Agric. 94(13): 2639–2648.
Fuentes, L., Valdenegro, M., Gómez, M.G., Ayala-Raso, A., Quiroga, E., Martínez, J.P., Vinet, R.,
Caballero, E. and Figueroa, C.R. 2016. Characterization of fruit development and potential
health benefits of arrayan (Luma apiculata), a native berry of South America. Food Chem. 196:
1239–1247.
Funes, F. 1999. Estudio etnobotánico del Valle del Río Manso Inferior, provincia de Río Negro. UNComa,
CRUB, Bariloche, Argentina.
Guisinde, M. 1917. Medicina e higiene de los antiguos araucanos. Imprenta Universitaria. Chile.
Houghton, P.J. and Manby, J. 1985. Medicinal plants of the Mapuche. J. Ethnopharmacol. 13(1): 89–103.
Hurrell, J.A., Ulibarri, E.A., Delucchi, G. and Pochettino, M.L. 2010. Frutas: frescas, secas y preservadas.
Ed. LOLA, Buenos Aires, Argentina.
Jiménez-Aspee, F., Thomas-Valdés, S., Schulz, A., Ladio, A., Theoduloz, C. and Schmeda-Hirschmann,
G. 2015. Antioxidant activity and phenolic profiles of the wild currant Ribes magellanicum from
Chilean and Argentinean Patagonia. Food Sci. Nutr. 4(4): 595–610.
Jiménez-Aspee F., Theoduloz, C., Ávila, F., Thomas-Valdés, S., Mardones, C., von Baer, D. and
Schmeda-Hirschmann, G. 2016. The Chilean wild raspberry (Rubus geoides Sm.) increases
intracellular GSH content and protects against H2O2 and methylglyoxal-induced damage in AGS
cells. Food Chem. 194: 908–919.
Ladio, A. and Rapoport, E.H. 1999. El uso de plantas silvestres comestibles en una población suburbana
del noroeste de la Patagonia. Parodiana. 11(1-2): 49–62.
Ladio, A. and Lozada, M. 2000. Edible wild plant use in a Mapuche community of northwestern
Patagonia. Hum. Ecol. 28(1): 53–71.
Ladio, A. 2001. The Maintenance of Wild Edible Plant Gathering in a Mapuche Community of Patagonia.
Econ. Bot. 55: 243–254.
Ladio, A. and Lozada, M. 2001. Non-timber forest product use in two human populations from NW
Patagonia: A quantitative approach. Hum. Ecol. 29(4): 367–380.
Patagonian Berries 67
Ladio, A. and Lozada, M. 2003. Comparison of wild edible plant diversity and foraging strategies in
two aboriginal communities of northwestern Patagonia. Biodivers Conserv. 12: 937–951.
Ladio, A. and Lozada, M. 2004. Patterns of use and knowledge of wild edible plants in distinct ecological
environments: A case study of a Mapuche community from northwestern Patagonia. Biodivers
Conserv. 13(6): 1153–1173.
Ladio, A. 2005. Malezas exóticas comestibles y medicinales utilizadas en poblaciones del NO patagónico:
aspectos etnobotánicos y ecológicos. Bol. Latinoam Caribe Plant Med. Aromat. 4(4): 75–80.
Ladio, A. 2006. Gathering of wild plant foods with medicinal use in a Mapuche community of Northwest
Patagonia. pp. 297–321. In: Pieroni, A. and Price, L. (eds.). Eating and Healing: Traditional Food
as Medicine. The Haworth Press, New York, USA.
Ladio, A., Molares, S. and Rapoport, E. 2007. Conocimiento etnobotánico de plantas comestibles entre
los maestros patagónicos: patrones de variación ambiental oeste-este. Kurtziana 33(1): 141–152.
Ladio, A. and Lozada, M. 2008. Medicinal plant knowledge in rural communities of North-western
Patagonia, Argentina. A resilient practice beyond acculturation. Current Topics in Ethnobotany
661(2): 39–53.
Ladio, A. and Lozada, M. 2009. Human ecology, ethnobotany and traditional practices in rural
populations inhabiting the Monte region: Resilience and ecological knowledge. J. Arid. Environ.
73: 222–227.
Ladio, A. 2011. Underexploited wild plant foods of North-Western Patagonia. pp. 297–321. In: Filip,
R. (ed.). Multidisciplinary Approaches on Food Science and Nutrition for the XXI Century.
Transworld Re-search Network, Kerala, India.
Ladio, A., Molares, S., Ochoa, J. and Cardoso, B. 2013. Etnobotánica aplicada en patagonia: La
comercialización de malezas de uso comestible y medicinal en una feria urbana de San Carlos
de Bariloche (Río Negro, Argentina). Bol. Latinoam Caribe Plant Med. Aromat. 12(1): 24–37.
Ladio, A. and Molares, S. 2014. The dynamics of use of nontraditional ethnobiological products: Some
aspects of study. pp. 311–319. In: Albuquerque, U.P., Vital Fernandes Cruz da Cunha, L., Farias
Paiva de Lucena, R. and Nobrega Alves, R.R. (eds.). Methods and Techniques in Ethnobiology
and Ethnoecology. Springer Science.
Llano, C. and Barberena, R. 2013. Explotación de especies vegetales en la Patagonia septentrional:
El registro arqueobotánico de Cueva Huemul 1 (Provincia de Neuquén, Argentina). Darwiniana
1: 5–19.
Lozada, M., Ladio, A. and Weigandt, M. 2006. Cultural transmission of ethnobotanical knowledge in a
rural community of Northwestern Patagonia, Argentina. Econ. Bot. 60(4): 374–385.
Mahabir, S. 2014. Methodological challenges conducting epidemiological research on nutraceuticals
in health and disease. Pharma Nutrition. 2: 120–125.
Martínez-Crovetto, R. 1980. Apuntes sobre la vegetación de los alrededores del lago Cholila (Noroeste
de la Provincia de Chubut). Publicación Técnica, Universidad Nacional Del Nordeste Facultad
de Ciencias Agrarias, Corrientes, Argentina.
Martínez-Crovetto, R. 1982. Breve panorama de las plantas utilizadas por los indios de Patagonia y Tierra
del Fuego. Suplemento Antropológico Vol XVII. Nro. 1, Universidad Católica, Asunción 61–97.
Medeiros, M.F.T. 2009. Etnobotânica Histórica: Princípios e Procedimientos. NUPEEA/Sociedad
Brasileira de Etnobiología e Etnoecología, Recife, Brasil.
Meza, I.P. and Villagran, C. 1991. Etnobotánica de la Isla Alao, Archipielago de Chiloe, Chile. Bol.
del Mus. Nac. Chile. 42: 39–78.
Molares, S. and Ladio, A.H. 2009a. Ethnobotanical review of the Mapuche medicinal flora: Use patterns
on a regional scale. J. Ethnopharmacol. 122(2): 251–260.
Molares, S. and Ladio, A.H. 2009b. Plantas Medicinales de los Andes Patagónicos: una revisión
cuantitativa del conocimiento etnobotánico Mapuche. pp. 87–128. In: Vignale, N.D., Pochettino,
M.L. (eds.). Avances sobre Plantas Medicinales Andinas, CYTED, S.S. de Jujuy, Argentina.
Molares, S. and Ladio, A. 2012. The usefulness of edible and medicinal Fabáceae in argentine and
Chilean Patagonia: Environmental availability and other sources of supply. Evidence-based
Complement Altern. Med. eCAM. 2012; 2012: 901918.
Molares, S. and Ladio, A. 2014. Medicinal plants in the cultural landscape of a Mapuche-Tehuelche
community in arid Argentine Patagonia: an eco-sensorial approach. J. Ethnobiol. Ethnomed. 10: 61.
68 ETHNOBOTANY: Local Knowledge and Traditions
Molares, S. and Ladio, A.H. 2015. Complejos vegetales comestibles y medicinales en la Patagonia
Argentina: sus componentes y posibles procesos asociados. Bol. Latinoam Caribe Plant Med.
Aromat. 14(3): 237–250.
Mösbach, E.W. 1992. Botánica indígena de Chile. Ed. Andrés Bello, Santiago, Chile.
Muñoz, M.S., Barrera, E.M. and Meza, I.P. 1981. El uso medicinal y alimenticio de plantas nativas y
naturalizadas en Chile. Pub. Ocac. Mus. Hist. Natural de Chile. 33: 3–89.
Nacuzzi, L.R. and Perez de Micou, C. 1984. Los recursos vegetales de los cazadores de la cuenca del
Río Chubut. Cuad. del Inst. Nac. Antropol. 10: 407–423.
Ochoa, J.J., Ladio, A.H. and Lozada, M. 2010. Uso de recursos herbolarios entre Mapuche y criollos de
la comunidad campesina de Arroyo Las Minas (Río Negro, Patagonia Argentina). Bol. Latinoam
Caribe Plant Med. Aromat. 9(4): 269–276.
Ochoa, J.J. and Ladio, A.H. 2011. Pasado y presente del uso de plantas silvestres con órganos de
almacenamiento subterráneos comestibles en la patagonia. Bonplandia 20(2): 265–284.
Ochoa, J.J. 2015. Uso de plantas silvestres con órganos de almacenamiento subterráneos comestibles
en Patagonia: perspectivas etnoecológicas. Tesis doctoral, Universidad Nacional del Comahue,
Bariloche, Argentina.
Ochoa, J.J. and Ladio, A.H. 2015. Plantas silvestres con órganos subterráneos comestibles: transmisión
cultural sobre recursos subutilizados en la Patagonia (Argentina). Bol. Latinoam Caribe Plant
Med. Aromat. 14(4): 287–300.
Pandey, K.B. and Rizvi, S.I. 2009. Plant polyphenols as dietary antioxidants in human health and
disease. Oxid. Med. Cell. Longev. 2(5): 270–278.
Pardo, O. and Pizarro, J.L. 2005. Especies Botánicas consumidas por los Chilenos Prehispánicos.
Colección Chile Precolombino, Santiago, Chile.
Pochettino, M.L. 2015. Botánica económica. Las plantas interpretadas según tiempo, espacio y cultura.
Sociedad Argentina de Botánica, Corrientes, Argentina.
Prates, L. 2009. El uso de recursos por los cazadores-recolectores posthispánicos de Patagonia
continental. Relac la Soc Argentina Antropol. 34: 201–229.
Ragonese, A.E. and Martínez-Crovetto, R. 1947. Plantas indígenas de la Argentina con Frutos o Semillas
comestibles. Revista de Investigaciones Agrícola 1(3): 147–216.
Ramírez, J.E., Zambrano, R., Sepúlveda, B., Kennelly, E.J. and Simirgiotis, M.J. 2015. Anthocyanins
and antioxidant capacities of six Chilean berries by HPLC-HR-ESI-ToF-MS. Food Chem. 176:
106–114.
Rapoport, E. and Ladio, A. 1999. Los bosques andino-patagónicos como fuentes de alimento. Bosque
20(2): 55–64.
Rapoport, E.H., Ladio, A.H. and Sanz, E. 2003. Plantas nativas comestibles de la Patagonia andina
argentino-chilena. Parte II. Imaginaria, Bariloche, Argentina.
Rapoport, E.H., Ladio, A.H. and Sanz, E. 2005. Plantas nativas comestibles de la Patagonia andina
argentino-chilena. Parte I. Imaginaria, Bariloche, Argentina.
Richeri, M., Ladio, A.H. and Beeskow, A.M. 2013. Conocimiento tradicional y autosuficiencia: La
herbolaria rural en la meseta central del chubut (Argentina). Bol. Latinoam Caribe Plant Med.
Aromat. 12(1): 44–58.
Romanucci, V., D’Alonzo, D., Guaragna, A., Di Marino, C., Davinelli, S., Scapagnini, G., Di
Fabio, G. and Zarrelli, A. 2016. Bioactive compounds of Aristotelia chilensis Stuntz and their
pharmacological effects. Curr. Pharm. Biotechnol. 17(6): 513–523.
Rovere, A.E. 2006. Cultivo de Plantas Nativas Patagónicas: árboles y arbustos. Ed Caleuche. Bariloche,
Argentina.
Ruiz, A., Hermosín-Gutiérrez, I., Mardones, C., Vergara, C., Herlitz, E., Vega, M., Dorau, C.,
Winterhalter, P. and von Baer, D. 2010. Polyphenols and antioxidant activity of calafate (berberis
microphylla) fruits and other native berries from Southern Chile. J. Agric. Food Chem. 58(10):
6081–6089.
Ruiz, A., Hermosín-Gutiérrez, I., Vergara, C., von Baer, D., Zapata, M., Hitschfeld, A. and Mardones,
C. 2013. Anthocyanin profiles in south Patagonian wild berries by HPLC-DAD-ESI-MS/MS.
Food Res. Int. 51(2): 706–713.
San Martín, J.A. 1983. Medicinal plants in central Chile. Econ. Bot. 37(2): 216–227.
Patagonian Berries 69
Introduction
Medicinal plants are a subject of concern to researchers, traders, users and states
and, in general terms, the problems facing these species in the world are similar. On
one hand, a greater proportion is located in certain areas of the planet, in developing
countries and its use and conservation is linked to traditional cultures, implying
knowledge, beliefs and spirituality. On the other hand, the fact that most are wild
(40.5%) or naturalized (33.3%) and only 3.3% are cultivated (Singh et al. 2012)
means that their conservation depends mainly on collection pressure.
The most important risk factors for medicinal species in the world would
be competition for land use, which entails the destruction of natural habitats,
excessive collection due to the growth of market demand—a direct consequence
of the growth of the human population—and the increase of industrial products
derived from plants. This last factor implies permanent bio prospecting in searching
new medicinal compounds (Roberson 2008, Castle et al. 2014). Bio prospecting
leads to the risk of bio piracy. This means that large companies patent genetic
resources, remedies and traditional knowledge of local or indigenous populations
and commercialize them with great economic benefits, but with little or no benefit
There are five protected natural areas (San Andrés de Cutervo, Tabaconas-
Naballe, Pagaibamba, Udima and Sunchubamba) in the Cajamarca’s Region,
where 908 genera and 2699 plant species are housed (Sagástegui et al. 1999). Like
the Huánuco’s Region, it occupies the first place in endemism in Peru, with 948
species (17%). Of this total, 296 (31%) are rare species. Because of this rich flora,
it is a supplier of various vegetable resources and especially of medicinal plants for
the markets of the Peruvian coast. These medicinal species mainly come from the
Jalca, as demonstrated by the studies of Bussmann and Sharon (2006), Bussmann
et al. (2008), Bussmann and Sharon (2009), Ramírez et al. (2006), Vásquez et al.
(2010) and Sánchez (2011).
Since the 1970s, an aggressive intervention process of the Jalca has been
initiated through new human settlements, intensive grazing, burning of natural
pastures to provoke its regrowth (traditional peasant practice) and agriculture of
cereals and tubers. The disturbance of these ecosystems was accelerated in the
1990s, due to the intensification of open-pit mining (Ramírez et al. 2006, Seminario
and Sánchez 2010, Sánchez 2014). These mountains, in addition to their wealth
of flora and fauna, are rich in minerals such as gold, copper and silver. As a result,
besides the mining Yanacocha, a company operating in one of the largest gold
deposits of Latin America, there are another companies in exploration and operation,
although there are no official data on the total concessions.
In this scenario, the study by Vásquez et al. (2010), which documents in detail
the morphology, distribution and conservation status and uses of 130 medicinal
species of northern Peru, emphasizes that several wild medicinal species that are
harvested for the market are in the disappearing process. Among these, the authors
cited the valeriana (Valeriana pilosa), huamanripa (Senecio tephrosioides), vira vira
(Senecio canescens), azarcito (Isertia krausei), cascarilla (Cinchona pubescens),
añasquero (Dyssodia jelskii) and uña de gato (Uncaria tomentosa). However, some
of the mentioned species are not considered within the categorization of endangered
species of wild flora of Peru (DS-043-2006-AG 2006), so it is necessary to review
and update it.
The objective of this document is to summarize the advances of research in
medicinal plants in the Cajamarca's Region. This state of knowledge should serve
to know how much has been done and what remains to be done. For this purpose,
formal publications on medicinal plants of the region were revised, taking as a
starting point the studies of Luis Iberico at the beginning of the decade of 1980.
Also taken into account is some gray literature that, by the importance of the data,
allows a better vision of what has been done so far on the subject. Another special
consideration was that, in all cases, the determination of the botanical species was
directed or supported by the botanists A. Sagástegui Alva and I. Sánchez Vega and
was carried out in the herbaria of the National University of Cajamarca (Isidoro
Sánchez Vega), National Agrarian University La Molina (A. Weberbauer), National
University of San Marcos (Museum of Natural History) and the Antenor Orrego
Private University. From this review, a matrix with the 15 studies, the families and
the species was generated. This served for the corresponding analysis.
Status of Research on Medicinal Plants in the Cajamarca’s Region, Peru 73
The information is presented in three blocks. The first block exposes research
on the diversity of medicinal plants in the region. We have included here two
investigations that refer to floristic diversity: the first one was developed in the
province of Contumazá (Sagástegui 1995) with its eight districts and the second
(Marcelo et al. 2006) one was realized in a Páramo of the province of Jaén. In the
first, a Chapter (8, p. 97–118) is dedicated to medicinal plants and in the second,
in the list of species, several species are known as medicinal in the region. The
second block summarizes research related to the market of medicinal species in
Cajamarca and, in the third block, specific studies on the use of medicinal species
in the region are presented.
N ECUADOR
l Ecuador
Colombia
PIURA
AMAZONAS Brasil
!19
Oc
ea
no
Pa
ci f
ico
!18
!17
LAMBAYEQUE
!16
!15
!22
!14
!13 !20
!24
!6 !8 !23 !12
!1 !7 !5 !4
!25 !26
!2 !3 !10 !21
!11
!9
Fig. 5.1. Map of the Cajamarca´s Region, indicating the districts where the studies on medicinal
plants were carried out.
Table 5.2. Medicinal plant families of the Cajamarca’s Region, mentioned in 15 studies.
of Cajamarca were native to the Americas—and mainly from the Andes—and 33%
came from other continents. 45% of registered species were wild (most of them
came from Jalca). The rest were domesticated in different degrees: cultivated,
wild-cultivated, wild-arvense, arvense.
Diseases or conditions that involved a greater number of plant species were
the woman’s diseases, gynecological in general, diseases of the urogenital system
and inflammatory, mainly of the respiratory and gastrointestinal system. The most
used plant part was the leaf. It was followed by the leaf plus reproductive organs,
the whole plant and the reproductive organs alone. The preponderant forms of
preparation were infusion and cooking, and the main form of administration was
as a beverage and to a lesser extent in plaster, poultice and rub.
The most important places for collecting medicinal species were Encañada,
Otuzco, Cumbemayo, Combayo, Llacanora, San Juan and Jesus. The most exported
78 ETHNOBOTANY: Local Knowledge and Traditions
Table 5.3. Medicinal species of the Jalca of Cajamarca, with greater demand in the market (2010).
The emollient’s origins are not clear. However, it is known that in 1927, there
was already in Lima the Society of Emollient Makers, which would have been
created with the support of the Japanese colony. Because of this, it was said that
the Japanese people brought emollient to Peru.
Bussman et al. (2015) and Ríos et al. (2017) suggest that the emollient would
be the same as horchata, a drink made from tubers of chufa (Ciperus esculentus)
whose origins would be in ancient Egypt (2400 BC) from where it moved to Europe
and then to America with the conquest. In Latin America, this drink has different
compositions, depending on the country or region, and usually includes a grain or
seed (barley, rice, almonds, more cinnamon and sugar). Ríos et al. (2017) indicate
that in the south of Ecuador, the horchata is an infusion of herbal mixture prepared
with 16 to 32 herbs plus sugar, honey or unrefined sugar cane and some drops of
lemon. However, this drink is different from the Peruvian emollient, which is a drink
formed by a syrup or concentrated juice of a plant—for example lemon, flaxseed,
cat’s claw, chicory, aloe, grade blood–plus a liquid, product of the cooking of several
plants or parts thereof—for example grains of barley, chamomile, horsetail, dog
foot, apple, pineapple, quince—which is drunk for food and therapeutic purposes.
In total, it can involve up to 15 plants at the same time. Also, the purposes are
different since you can approach the three-wheeled carriages and ask the seller for
a preparation for the kidneys, liver or stomach, depending on the condition you
have or to recover after a bad night. In each case, the base liquid is the same, but
the syrup will be different.
Status of Research on Medicinal Plants in the Cajamarca’s Region, Peru 81
Between the years 1995 and 2001, in the city of Cajamarca, the ambulatory
sale of maca juice, aloe extract, quinoa shampoo and orange juice was established.
Evaluations between the years 2001 and 2003 showed that these five drinks involved
a variable number of plant species and three-wheeled carriages in the city (Table 5.4).
This ambulatory activity employed 126 families and included 58 plant species (38
plant families and 57 genera)—trees, shrubs, grasses and lianas—cultivated and
wild, 60% of them being of American origin.
Substantial changes in the system of these beverages, with respect to production
and collection, preparation and the market, are likely to have occurred to date, and
information needs to be updated. For example, in the last years the sale of sugar
cane juice, pineapple, grapefruit and melon has been observed.
On the other hand, the Municipality of Cajamarca has paid attention to
and trained business drivers on food handling. Moreover, on May 17, 2014, the
Peruvian government promulgated the Emollient maker Law (N° 30198), which
recognizes these ventures as self-productive employment microenterprises and
establishes February 20 as the day of emollient, quinoa, maca, kiwicha and other
traditional natural drinks. Another important issue is that more than 30% of Lima’s
emollient makers are people from Cajamarca (Cajamarquinos) (Bussmann et al.
2015). This confirms the role of Cajamarca’s families in the diffusion of this drink.
Likewise, preliminary observations indicate that people from Cajamarca, mainly
from Bambamarca, have taken this business to Ecuador (e.g., Quito and Cuenca),
where it is sold as an emollient—not as horchata—and has achieved remarkable
development. Undoubtedly, the subject has ethnobotanical, economic, social,
phytochemical, and public health perspectives that must be studied in detail.
Table 5.4. Number of three-wheeled carriages and species involved in the emollient, maca juice, aloe
extract and orange juice, in the city of Cajamarca: 2001 and 2003.
was investigated. They found that peasants of these localities used 14 plant species
for this purpose, of which 10 were native—all wild—and four exotic (Table 5.5).
In four communities in the district of Huambos, province of Chota, an
investigation was carried out to identify medicinal plants used for gynecological
purposes in women—menstruation, fertility, delivery, postpartum and gynecological
diseases (Ramos 2015). 39 plant species were used for this purpose, 28 of them
were wild and native at the same time: 11 shrubs, 5 trees, 22 herbs and 1 succulent.
Asteraceae was the most representative family with eight species, followed by
Lamiaceae and Poaceae with three species each. Three species (Gnaphalium dysodes
Spreng, Juglans neotropica Diels, Mauria heterophylla Kunth) are considered
within one of the three IUCN and DS043-2006-AG categories of endangered
species, one is endemic for Cajamarca and another is endemic for Cajamarca and
La Libertad departments. The number of species according to 15 use categories is
presented in Table 5.6.
Table 5.5. Plant species used in birth control in two communities of San Marcos, Cajamarca.
Conclusions
The studies on medicinal plants in the Cajamarca's region had an ethnobotanical
focus, mainly directed to know the diversity of the species, the market and the uses.
The studies cover the ecological regions of Yunga, Quechua and Jalca, with
predominance towards the species of Jalca. They cover 16% of the districts of the
Cajamarca’s region and were developed mainly in the provinces of Cajamarca
and Contumazá.
In 15 reviewed studies, 457 species in 105 families and 296 genera were
recorded. Most species are wild and native to the Andes. The best represented
families were Asteraceae, Lamiaceae, Fabaceae, Solanaceae, Rosaceae and
Piperaceae.
The most frequently mentioned species in the studies were Ishpingo
verde (Achyrocline alata), manzanilla (Matricaria chamomilla), cola de
caballlo (Equisetum bogotense), pie de perro (Desmodium mollicum), chancua
(Minthostachys mollis), hinojo (Foeniculum vulgare), ajenjo (Artemisa absintium),
carqueja (Baccharis genistelloides), escorzonera (Perezia multiflora), cerraja
(Sonchus oleraceus), orégano (Origanum vulgare) and llantén (Plantago major).
86 ETHNOBOTANY: Local Knowledge and Traditions
Acknowledgments
To Rosel Orrillo for his support in the data collection and map elaboration.
To Juan Montoya (Herbarium Isidoro Sánchez Vega-UNC) for his collaboration
with important documents.
References
Aguilar, I. 2017. Análisis estadístico de la productividad del germoplasma de yacón Smallanthus
sonchifolius (Poepp. & Endl.) H. Robinson de la UNC. Tesis Ing. Agr. Cajamarca, PE, Facultad
de Ciencias Agrarias, Universidad Nacional de Cajamarca. 127 p.
Aldave, M.A. 2003. Aspectos etnobotánicos de las plantas medicinales en la ciudad de Cajamarca. Tesis
Ing. Agr. Cajamarca, PE, Facultad de Ciencias Agrarias, Universidad Nacional de Cajamarca. 72 p.
Alvarez, P., Jurado, B., Calixto, M., Incio, N. and Silva, J. 2008. Prebiótico inulina/oligofructosa en la
raíz del yacón (Smallanthus sonchifolius) fitoquímica y estandarización como base de estudios
preclínicos y clínicos. Rev. Gastroenterol. Perú 28: 22–27.
Alvitres, K., Huamán, I.M. and Vera, L. 2007. Plantas medicinales, biocidas y aromáticas del Distrito de
La Encañada, Cajamarca. Tesis Licenciado en Educación. Cajamarca, PE. Facultad de Educación,
UNC. 109 p.
Arnao, I., Seminario, J., Cisneros, R. and Trabuco, J. 2011. Potencial antioxidante de 10 accesiones de
yacón (Smallanthus sonchifolius (Poepp. & Endl.) Robinson) procedentes de Cajamarca, Perú.
An. Fac. Med. 72(4): 239–243.
Ayasta, D.M. 2012. Memoria e identidad: El caso de los cuspiniques. Librosperuanos.com. Consulta
22-11-2016. Disponible en http://www.librosperuanos.com/autores/articulo/00000002088/
Memoria-e-Identidad-El-caso-de-los-Cupisnique.
Ayay, J.I. 2017. La agrobiodiversidad en la agricultura familiar del caserío Chilincaga, Centro Poblado
Porcón Bajo, Cajamarca. Tesis Ing. Agr. Cajamarca, PE. Facultad de Ciencias Agrarias, Universidad
Nacional de Cajamarca. 130 p.
Blas, R., Ghislain, M., Herrera, M.R. and Baudoin, J.P. 2008. Genetic diversity analysis of wild
Arracacia species according to morphological and molecular markers. Genet. Resour Crop.
Evol. 55: 625–642.
Bussmann, R.W. and Sharon, D. 2006. Traditional medicinal plant use in Northern Peru: Tracking two
thousand years of healing culture. Journal of Ethnobiology and Ethnomedicine 2: 47. Consultado
29-08-2014. Disponible en: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637095/.
Bussmann, R.W., Sharon, D. and Ly, J. 2008. From garden to market? The cultivation of native and
introduced medicinal plant species in Cajamarca, Peru and implications for habitat conservation.
Ethnobotany Research & Applications 6: 351–361. Consultado 27-07-2017. Disponible en: https://
www.researchgate.net/publication/29744682. DOI: 10.17348/era.6.0.351-361.
Bussmann, R.W. and Sharon, D. 2009. Markets, healers, vendors, collectors: The sustainability of
medicinal plant use in northern Peru. Mountain Research and Development (MRD) 29(2): 128–134.
Status of Research on Medicinal Plants in the Cajamarca’s Region, Peru 87
Bussmann, R.W., Paniagua-Zambrana, N., Castañeda, R.Y., Prado, Y.A. and Mandujano, J. 2015. Healt
in a pot—the ethnobotany of emolientes and emolienteros in Peru. Notes on economic plants.
Economic Botany 69(1): 83–88.
Camino, L. 1992. Cerros, plantas y lagunas poderosas. La medicina al norte del Perú. Lluvia Editores,
Lima, PE. 296 p.
Castañeda, D.T. and Vargas, M.L. 1991. Uso de plantas medicinales y otros métodos para el control de la
natalidad: su conocimiento en los caseríos de Milco y Shitabamba de la provincia de San Marcos:
1987–1991. Tesis Lic. Sociología, Cajamarca, PE, Facultad de Ciencias Sociales, Universidad
Nacional de Cajamarca. 110 p.
Castañeda, G.M. and Condori, E.M. 2010. Catálogo y estudio farmacognóstico de plantas medicinales
del distrito de Llacanora, Provincia de Cajamarca, Departamento deCajamarca. Tesis Químico
Farmacéutico. Lima, PE. Facultad de Farmacia y Bioquímica, UNMSM. 154 p.
Castillo-Vera, H., Cochachín, E. and Albán, J. 2017. Plantas comercializadas por herbolarios en el
mercado del distrito de Cajabamba (Cajamarca, Perú). Blacpma 16(3): 303–318.
Castle, L.M., Leopold, S., Craft, R. and Kindscher, K. 2014. Ranking tool created for medicinal plants
at risk of being overharvested in the wil. Ethonobioloy Letters 5: 77–88. Consultado 28-07-2017.
Disponible en http://ojs.ethnobiology.org/index.php/ebl/article/view/169.DOI:10.14237/ebl.5.
Choque, G.T., Thome, R., Gabriel, D.L., Tamashiro, W.M.S.C. and Pastore, G.M. 2012. Yacon
(Smallanthus sonchifolius)-derived fructooligosaccharides improves the immune parameters in
the mouse. Nutrition Research 32: 884–892.
Choque, G.T., Silva, W.M.S.C., Maróstica, M.R. and Pastore, G.M. 2013. Yacon (Smallanthus
sonchifolius): A funtional food. Plant Foods Hunt Nutr. 68: 222–228.
DS-043-2006-AG. 2006. Categorización de especies amenazadas de flora silvestre. DiarioOficial El
Peruano, 13 julio 2006.
Foy, E. 2005. Smallanthus sonchifolius (llacón o yacón) en el tratamiento de hiperlipoproteinemias e
hipercolesterolemia inducidas en ratas albinas. Rev. Fac. Mmed. Hum. 5(1): 27–31.
Iberico, L. 1881. El folklore agrario de Cajamarca. Universidad Nacional de Cajamarca, pp. 65–72.
Iberico, L. 1984. Folklore médico de Cajamarca. Universidad Nacional de Cajamarca. 238 p.
La Torre, M.A. 1998. Etnobotánica de los recursos vegetales silvestres del caserío de Yanacancha,
distrito de Chumuch, provincia de Celendín, Cajamarca. Tesis Biólogo, Facultad de Ciencias,
Universidad Nacional Agraria La Molina. 50 p.
Lebeda, A., Doležalová, I., Fernández, E. and Viehmannová, I. 2011. Yacon (Asteraceae; Smallanthus
sonchifolius). Chapter 20. In: R.J. Singh (ed.). Genetic resources, chromosome engineering, and
crop improvement: Medicnal plants. Vol. 6. Taylor & Francis Group, London.
León, B., Roque, J., Ulloa, C., Jorgenson, P.M., Pitman, N. and Cano, A. (eds.). 2006. El libro rojo de
las plantas endémicas el Perú. Rev Peru Biol 13 (2). Número especial.
Ley 30198. Ley que reconoce la preparación y expendio o venta de bebidas elaboradas con plantas
medicinales en la vía pública, como microempresas generadoras de autoempleo productivo. Diario
Oficial El Peruano. Normas Legales. 17 de mayo, 2014.
Marcelo, J.L., Sánchez, I. and Millán, J. 2006. Estado de la diversidad florística del Páramo sectores:
El Espino y Palanque, Sallique, Jaén, Cajamarca, Perú. Ecología Aplicada 5(1,2): 1–8.
Martínez Compañon, B.J. 1789. Codex Trujillo del Perú. Vol. V. Biblioteca Nacional de
Colombia. Biblioteca digital. Disponible en: http://www.bibliotecanacional.gov.co/
content/%E2%80%9Ccodex-trujillo-del-per%C3%BA%E2%80%9D.
Montoya, E. and Figueroa, G. 1991. Geografía de Cajamarca. Vol. II. Taller de Estudio Fanny Abanto
Calle, Lima, PE. 359 p.
Nazar, J. and Alva, E. 2015. Efecto del encalado en el crecimiento de Valeriana pilosa R. & P. en
Huanico, Cajamarca. Fiat Lux 11(2): 53–59.
Orozco, O. 2003. Poisons plants and type uses in Cajamarca, Peru. A dissertation submitted to the
Graduate Faculty in Biology in partial fulfillment of the requirements for the degree of Doctor of
Phylosophy, The City University of New York. 304 p.
Pulgar Vidal, J. 1996. Las ocho regiones naturales del Perú. PEISA, Lima, PE. 302 p.
Ramírez, J.P., Terán, R.M., Sánchez, I. and Seminario, J. 2006. Etnobotánica de la valeriana (Valeriana
spp.) en la Jalca de Cajamarca, Perú. Arnaldoa 13(2): 368–379.
88 ETHNOBOTANY: Local Knowledge and Traditions
Ramos, G.E.V. 2015. Plantas medicinales de uso ginecológico de cuatro comunidades del distrito de
Huambos, provincia de Chota, departamento de Cajamarca. Tesis biólogo. Lima, PE. Facultad
de Ciencias, Universidad Nacional Agraria, La Molina. 169 p.
Revene, Z., Bussmann, R.W. and Sharon, D. 2008. From sierra to coast: Tracing the supply of medicinal
plants in northern Peru—A plant collector’s tale. Ethnobotany Research and Application 6: 15–22.
Consultado 10-09-2014. Disponible en: www.ethnobotanyjournal.org/ vol6/i1547-3465-06-015.
pdf.
Ríos, M., Tinitana, F., Jarrín, P., Donoso, N. and Romero-Benavides, J.C. 2017. “Horchata” drink
in southern Ecuador: medicinal plants and peoples’s wellbeing. Journal of Ethnobiology and
Ethnomedicine 2017:13–18. Consultado 05-08-2017. Disponible https://link.springer.com/content/
pdf/10.1186%2Fs13002-017-0145-z.pdf DOI:10.1186/S13002-017-0145-Z.
Rojas, J.M. and Seminario, J. 2014. Método alométrico para estimar el área foliar de “valeriana”
(Valeriana pilosa R. & P.) al estado silvestre. Arnaldoa 21(2): 305–316.
Roberson, E. 2008. Medicinal plants at risk. Tucson. Centre for Biological Diversity. Consultado
28-07-2017. Disponible en: http://www.biologicaldiversity.org/publications/papers/Medicinal_
Plants_042008_lores.pdf.
Rumay, D. and Seminario, J. 2015. Respuesta de Valeriana pilosa R. & P a tres tratamientos agronómicos.
Fiat. Lux. 11(2): 101–110.
Sagástegui, A. 1995. Diversidad florística de Contumazá. Universidad Privada del Norte, Fondo
Editorial. Trujillo, Perú. 203 p.
Sagástegui, A., Dillon, M.O., Sánchez, I., Leiva, S. and Lezama, P. 1999. Diversidad florística del norte
del Perú. Tomo I. WWF (World Wildlife Fund). Lima, PE. 228 p.
Sánchez, I. and Dillon, M. 2006. Jalcas. pp.77–90. In: Moraes, M., Øllarard, B., Kvist, P., Borchsenius,
F. and Balslev, H. (eds.). Botánica Económica de los Andes. Universidad Nacional de San Andrés,
La Paz, Bolivia.
Sánchez, I. 2011. Especies medicinales de Cajamarca I. Contribución etnobotánica, morfológica y
taxonómica. Universidad Privada Antonio Guillermo Urrelo, Lumina Cooper Fondo Editorial.
228 p.
Sánchez, I. 2014. Plantas medicinales en los páramos de Cajamarca. pp. 175–194. In: Cuesta, F.,
Sevink, J., Llambi, L.D., de Bièvre, B. and Posner, J. (eds.). Avances en Investigación Para la
conservación de los páramos andinos.
Satoh, H., Audrey, M.T., Kudoh, A. and Watanabe, T. 2013. Yacon diet (Smallanthus sonchifolius,
Asteraceae) improves hepatic insulin resistance via reducing Trb3 expression in Zuker fa/fa rats.
2013. Nutrition & Diabetes 3. Consultado 27-07-2017. Disponible en http://www.nature.com/
nutd/journal/v3/n5/full/nutd201311a.html?foxtrotcallback=true. DOI:10.1038/nutd.
Singh, R.J. 2012. Landmark research in medicinal plants (cap. 1). pp. 1–11. In: Singh, R.J. (ed.). Genetic
Resources, Chromosome Engineering, and Crop Improvement. Medicinal Plants.
Singh, R.J., Lobeda, A. and Tucker, A.O. 2012. Medicinal plants—nature’s pharmacy. pp. 14–51.
In: Singh, R.J. (ed.). Genetic Resources, Chromosome Engineering, and Crop Improvement.
Medicinal Plants.
Singh, R.D., Mody, S.K., Patel, H.B., Devi, S., Modi, C.M. and Kamani, D.R. 2014. Pharmaceutical
biopiracy and protection of traditional knowledge. Int. J. Res. Dev. Pharm. L. Sci. 3(2): 866–871.
Seminario, J., Valderrama, M. and Manrique, I. 2003. El yacón. Fundamentos para el aprovechamiento
de un recurso promisorio. CIP (Centro Internacional de la Papa), UNC (Universidad Nacional de
Cajamarca), COSUDE (Cooperación Suiza al Desarrollo), Lima, PE. 57 p.
Seminario, J. and Valderrama, M. (eds.). 2003. I Curso Nacional Cultivo y Aprovechamiento del Yacón.
Cajamarca, 26 al 29 agosto 2002. 113 p.
Seminario, J. and Valderrama, M. 2004a. Variabilidad morfológica y distribución geográfica de
la colección de arracacha (Arracacia xanthorrhiza Bancroft) de la Universidad Nacional de
Cajamarca, Perú. Arnaldoa 11(2): 79–104.
Seminario, J., Valderrama, M. and Romero, J. 2004b. Variabilidad morfológica y distribución geográfica
del yacón, Smallanthus sonchifolius (Poepp. & Endl.) H. Robinson, en el norte peruano. Arnaldoa
11(1): 139–160.
Status of Research on Medicinal Plants in the Cajamarca’s Region, Peru 89
Seminario, J. 2004. Etnobotánica del emoliente y otras bebidas de venta ambulatoria en la ciudad de
Cajamarca. Caxamarca 12(1): 9–28.
Seminario, J., Rumay, L.D. and Seminario, A. 2016. Biología de Valeriana pilosa R. & P. (Valerianaceae):
una especie en peligro de extinción de las altas montañas de Perú. Bol. Latinoam Caribe Plant
Med. Aromat. 15(5): 337–351.
Seminario, J., Oblitas, I. and Escalante, B. 2017. Area foliar del yacón (Smallanthus sonchifolius
(Poepp. & Endl.) H. Rob.) estimada mediante método indirecto. Agron. Mesoam. 28(1): 171–181.
Seminario, A. and Sánchez, I. 2010. Estado y factores de riesgo de la biodiversidad de especies vegetales
medicinales en el Centro Poblado de Combayo, Cajamarca. Fiat. Lux. 6(1): 23–34.
Seminario, A. and Escalante, B. 2017. Potencial de la flora medicinal silvestre con fines de conservación
en el distrito La Encañada, Cajamarca. Fiat. Lux. 12(1). In press.
Sook, J. and Han, K. 2013. The spermatogenic effect of yacon extract and its constituents and their
inhibition effect of testosterone metabolism. Biomolecules & Therapeutics 21(2): 153–160.
Tinitana, F., Ríoss, M., Romero Benavides, J.C., De la Cruz, M. and Pardo, M. 2016. Medicinal plants
sold at traditional markets in southern Ecuador. J. Ethnobiology and Ethnomedicine 2016: 12–29.
Consultado 04-08-2017. Disponible en https://www.researchgate.net/publication/304915895_
Medicinal_plants_sold_at_traditional_markets_in_southern_Ecuador. DOI:10.1186/s13002-
016-0100-4.
Towle, M. 1961. The ethnobotany of pre-columbian Peru. Aldine publishing Company, Chicago, US.
180 p.
Ugent, D. and Ochoa, C.M. 2006. La etnobotánica del Perú. Desde la prehistoria al presente. Concytec.
Lima, PE. 380 p.
Valderrama, M. and Seminario, J. 2002. Los parientes silvestres de la arracacha (Arracacia xanthorrhiza
Bancroft) y su uso en medicina tradicional en el norte peruano. Arnaldoa 9(1): 67–91.
Valdez, H. 2017. Caracterización morfológica y germinación de la semilla de valeriana (Valeriana pilosa
R. & P.). Tesis Ing. Agr, Cajamarca, PE. Facultad de Ciencias Agrarias, Universidad Nacional
de Cajamarca. 62 p.
Valentova, K. and Ulrichová. 2003. Smallanthus sonchifolius and Lepidium meyenii prospective andean
crops for the prevention of chronic diseases. Biomed. Papers 147(2): 119–130.
Vásquez, L., Escurra, J., Aguirre, R., Váquez, G. and Vásquez, L.P. 2010. Plantas medicinales del norte
del Perú. FINCTYC, UNPRG, Lambayeque, PE. 382 p.
Watanabe, S. 2002. El reino de Cuismancu: orígenes y transformación en el Tahuantinsuyo. Boletín de
Arqueología PUCP n° 6: 107–136.
Weberbauer, A. 1945. El mundo vegetal de los Andes peruanos. Estudio fitogeográfico. Estación
Experimental Agrícola La Molina. Dirección de Agricultura. Ministerio de Agricultura. 2 ed.
Talleres Gráficos de la Editorial Lumen S.A. Lima, PE.
Yacovleff, E. and Herrera, F.L. 1934. Botánica etnológica (3). El mundo vegetal de los antiguos peruanos.
Revista del Museo Nacional 3(3): 243–322.
CHAPTER 6
Recent Reports on
Ethnopharmacological
and Ethnobotanical Studies
of Valeriana carnosa Sm.
(Valerianaceae)
Soledad Molares,1,* Ana H. Ladio2 and Nicolás Nagahama3
Introduction
In southernmost South America, both in Argentinean and Chilean Patagonia,
subterranean organs of numerous species of plants have long been recognized as
being of great value to Mapuche and Tehuelche regional ethnic groups and rural
Creole (Ladio and Lozada 2009, Molares and Ladio 2009a, Ochoa and Ladio 2011).
These species also constitute an important part of many regional rites and legends
(Ochoa and Ladio 2014).
From the perspectives of economic botany and ethnopharmacology, the main
value of these species is based on the fact that their subterranean organs often
contain starch and other carbohydrates of importance to the human diet, and also
therapeutic compounds derived from plant secondary metabolism (Gurib-Fakim
1
CIEMEP (Centro de Investigación Esquel de Montaña y Estepa Patagónica). Universidad Nacional
de la Patagonia San Juan Bosco-CONICET. Roca 780 Esquel, Chubut. Argentina.
2
Laboratorio Ecotono. INIBIOMA (Instituto de Biodiversidad y Medio Ambiente). Universidad
Nacional del Comahue-CONICET. Quintral 1250-S.C. de Bariloche, Rio Negro. Argentina.
3
Estación Experimental Agroforestal Esquel. Instituto Nacional de Tecnología Agropecuaria-CONICET.
Chacabuco 513. Esquel, Chubut, Argentina.
* Corresponding author: [email protected]
Ethnopharmacology and Ethnobotany of Valeriana carnosa 91
2006). Amongst these species, some representatives of Valeriana L. genus have been
used as medicinal plants, with high cultural and symbolic value. The underground
organs of many Valeriana species contain numerous compounds and are used
as a sedative and for treating insomnia, allowing the reduction of nervousness
and agitation associated with stress (Thies and Funke 1966, Wagner et al. 1980,
Nahrstedt 1984, Grusla et al. 1986, Upton 1999). This genus is widely studied, with
special focus on anxiolytic properties (Hattesohl et al. 2008, Murphy et al. 2010).
For anxiolytic purposes, since ancestral times, extracts of rhizomes and
roots of the Eurasian species V. officinalis L. have been used worldwide. Roots of
V. officinalis are used for treatment of anxiety and mild sleep disorders. Studies
indicate that flavonoids in this species have sedative activity in the central nervous
system (Marder et al. 2003, Fernández et al. 2004, 2005, 2006, Lacher et al. 2007).
Others authors suggests that biochemical composition and active constituents in
Valeriana are valepotriates (Backlund and Moritz 1998), valeric acid and gamma-
aminobutyric acid (Hallam et al. 2003, Nam et al. 2013). Besides, pre-clinical
studies reported the antidepressant-like activity of V. officinalis (Hattesohl et al.
2008), V. jatamansi Jones (Subhan et al. 2010, Sah et al. 2011), V. glechomifolia
Mey. (Müller et al. 2012) and V. prionophylla (Holzmann et al. 2011).
Currently, alternatives to V. officinalis are being sought in different countries for
replacement by indigenous representatives, for example, in India with V. jatamansi,
in Mexico with V. edulis Nutt. ex Torr. & A. Gray subsp. procera (Kunth) G.F. Mey
and in Brazil with V. glechomifolia (Bos et al. 1999, Oliva et al. 2004).
In Patagonia, there are records of the use of at least five native species of
Valeriana for medicinal purposes (Conticello et al. 1997, Molares and Ladio
2008). Among them, the most used Valeriana species by regional ethnic groups
is V. carnosa Sm. (“Ñamkulawen”, which means the white hawk medicine in
Mapuzungun language, probably in reference to the high sites where the species
grows and where the ñamku-Buteo polyosoma-can be seen in flight) and is
considered a “sacred plant” (Estomba et al. 2005, Molares and Ladio 2008)
(Fig. 6.1). This local name (Ñamkulawen) is shared with V. clarionifolia but this
plant has different reputed attributes. Another local name is “Valeriana”, which is
used by some Creole settlers.
Valeriana carnosa stands out as one of the principal elements in the indigenous
pharmacopoeias of Patagonia, and its roots and rhizomes have been used since
ancient times (Molares and Ladio 2009b). The local perception of this plant is
that it has wide-ranging curative powers: “it’s a cure-all”. This attribute confers
on the species high cultural and symbolic value for the Mapuche people, and its
reputation and use has spread throughout the formal and informal medicinal herb
market of Patagonian cities (Ladio 2006).
92 ETHNOBOTANY: Local Knowledge and Traditions
Fuego provinces. Its altitudinal range is from 0 m.a.s.l. to 2,700 m.a.s.l. (Zuloaga
et al. 2008). In phytogeographic terms, it is found in the Sub-Antarctic, Patagonian
and High-Andean provinces (Borsini et al. in Correa 1999).
The species flourishes in xeric, open, sunny environments in the rocky soils of
the forest, steppe and the Patagonian-Andean forest-steppe ecotone. It is also found
in sandy sites, on low, sunny slopes or even in rocky sites of the Patagonian Andes.
It flowers from October to December and fruits during the months of January and
February (Borsini et al. in Correa 1999, Kutschker 2011).
In spite of the wide geographic distribution of this species, gathering carried
out by the settlers is characterized by the search for specimens in stony areas with
a high level of light exposure, preferably at the highest altitude possible. The
underground part is collected with the help of simple tools like knives and spades.
In the process of identification and selection of specimens, cultural practices of
sensory perception come into play. These include the recognition of organoleptic
qualities directly associated with this species, such as its bitter and unpleasant smell
(“like dirty feet”) and its strong, bitter, repulsive flavor (“füre”), which is rather
spicy (“trapi”) and astringent (“seco”) (Molares and Ladio 2009a).
Various studies indicate that the collection of this species is associated with
the care of livestock. People take advantage of the time during which their animals
are grazing to look for the plant in places far from their dwellings (Estomba et
al. 2006, Richeri et al. 2013). With regard to the identification and collection of
V. carnosa and V. clarionifolia by Patagonian inhabitants, studies reveal levels of
organoleptic differentiation between the two species, which are of great cultural
and ethnopharmacological value. For example, it was discovered that locals are
capable of differentiating between Valeriana species, and that even though they
recognize them as related (which can be deduced by the fact that both have the
same common name), they can tell them apart by their smell and taste, which
consequently determine their different uses and value (Molares and Ladio 2012).
Unlike V. carnosa, V. clarionifolia is used for a limited number of ailments, mainly
to relieve lower back pain and treat kidney and bladder disorders and cultural
syndromes. In a curiously similar way, by means of laboratory tests with electronic
noses, differences between the aromatic profiles of V. carnosa and V. clarionifolia
have been found, which are determined by the chemical differences between the
species (Baby et al. 2005).
The collected pieces of V. carnosa are usually taken to the dwellings where
they are dried in the open air and in the shade, under cover, to be preserved later
in mesh or paper bags. This practice ensures availability of the dried resource all
year round, and is particularly useful in winter when the search for medicinal herbs
on the mountains can become difficult due to the accumulation of snow (Molares
and Ladio 2012).
Although V. carnosa gathering is very important and its commercialization has
increased rapidly over the last decades (Cuassolo 2009), this species can be regarded
as not threatened. However, settlers say that in some regions it is increasingly
difficult to find plants, and that longer distances must be travelled in the search
Ethnopharmacology and Ethnobotany of Valeriana carnosa 95
for them (Estomba et al. 2005, 2006). For this reason, the study of this plant’s
cultivation requirements must be encouraged (Cuassolo 2009). Currently, keeping
in view the importance of this species, a simple low cost technique using rooting
hormones for vegetative production of V. carnosa through macro-propagation has
been developed (Fig. 6.2) (Nagahama et al. 2016). Additionally, these authors
identified potential habitats of V. carnosa along the Argentine Patagonian with
predicting models for its cultivation in order to obtain potential marketable font
of phytomedicines and strengthen the non-conventional productive development
in Patagonia (Nagahama et al. 2016).
have isolated caffeoyl methyl ester and two pinoresinol-type lignans. Fajardo et al.
(2010) have also suggested that in terms of its biological activity, it would present
cytotoxic activity and negative toxicological activity. Guajardo et al. (2018) suggests
that phenolic compounds vary quantitatively and qualitatively between populations
as well as among plants’ phenological stages. Regarding the total phenol content,
the values obtained in V. carnosa (from ethanolic root extracts) varied between
3.3–14.3 mg eq GAE/g dry material, being similar to those reported for root
extracts in other species of medicinal use within the family Valerianaceae such
as V. officinalis (14.2 mg eq GAE/g dry material; Surveswaran et al. 2007) and
V. jatamansi (8.7 to 14.6 mg eq GAE/g dry material; Jugran et al. 2013).
Taking account of the above information, the traditional and recommended
method of use, which consists of the decoction of a handful of the material, followed
by ingestion of one cupful, orally, over a variable timeframe (Cuassolo 2009,
Cuassolo et al. 2011), Kutschker et al. (2002) propose uses of the plant in modern
medicine by means of the preparation of tinctures. The crude drug consists of
dried pieces of the roots and rhizomes. Kutschker et al. (2002) describes a dosage
of a daily cupful drunk on an empty stomach for a week. The roots are placed in
a jar with 300 ml of alcohol, left for 15 days and then filtered. The recommended
dosage is 1 to 2 ml as a sedative.
Fig. 6.3. Diagram of the aerial parts of the plant (a), floral structures (b and c) and fruit (d) of
V. carnosa Sm. (Taken from Borsini et al. in Correa 1999).
presented cork with irregular polygonal cells with acute and obtuse angles, while
in V. clarionifolia rectangular cork cells with right angles were observed. Starch
grains are simple, spherical in V. carnosa and polyhedral in V. clarionifolia. In
addition, Molares and Ladio (2012) studied cross sections of V. carnosa primary
root and observed a well-developed periderm consisting of cells with thickened,
birefringent walls, from irregular to polygonal; cells of this tissue and phloem
parenchyma have essential oils in the form of droplets (Sudan IV+); cortex has
large air spaces between oval cells with brown contents.
Conclusions
Valeriana carnosa is one of the most prominent medicinal plants in the Mapuche
tradition, and from an ethnopharmacological viewpoint, one of the most versatile
promising medicinal plants in Patagonia, when taking into account the wide range
of therapeutic alternatives it can offer for the treatment of the different ailments of
the region (Molares and Ladio 2009b, Richeri et al. 2013). However, V. carnosa is
not included in the Argentine Pharmacopoeia (http://www.anmat.gov.ar), nor does
it appear on the list of toxic species not recommended for consumption.
The similarity between the active compounds found in V. carnosa and
V. clarionifolia and those of V. officinalis is promising, since this species is included
worldwide in many pharmacopoeias and consumed orally as a sedative and sleep
inducer in humans. However, little conclusive evidence for the efficacy of the other
local uses can be provided. The key problem of various investigations has been
the emphasis on very few compounds rather than traditional preparations. Much
more research is required to evaluate the actual efficacy of the preparations. The
scientific research and cultural revalorization of the role played by V. carnosa in
local herbal medicines is of considerable ethnopharmacological interest and highly
relevant to the medicinal security of Patagonian communities. However, there is
evidence to indicate that the abundance of this species in natural environments is
decreasing, mainly due to disturbance of the environments (Estomba et al. 2006,
Ladio et al. 2007) and lack of regulation of its commercialization in Patagonian
cities (Cuassolo 2009). Given that the roots are the organs of medical interest in
this valuable species, the establishment of conservation strategies in situ and studies
that provide guidelines for its cultivation and preservation ex situ are of the utmost
importance (Nagahama et al. 2016).
Acknowledgements
We are profoundly grateful to the inhabitants of the rural and urban communities
where we learned about the ethnobotany of V. carnosa. This study was funded by
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET).
Ethnopharmacology and Ethnobotany of Valeriana carnosa 99
References
Baby, R.E., Cabezas, M., Kutschker, A., Messina, V. and Walsöe de Reca, N.E. 2005. Discrimination of
different valerian types with an electronic nose. J. Arg. Chem. Soc. The Journal of the Argentine
Chemical Society 93: 43–50.
Bach, H.G., Varela, B.G., Fortunato, R.H. and Wagner, M.L. 2014. Pharmacobotany of two Valeriana
species (Valerianaceae) of argentinian Patagonia known as “Ñancolahuen.” Lat. Am. J. Pharm.
33: 891–896.
Backlund, A.A. 1996. Phylogeny of the Dipsacales. Doctoral Dissertation. Dept. Systematic Botany,
Uppsala University, Sweden.
Backlund, A. and Moritz, T. 1998. Phylogenetic implications of an expanded valepotriate distribution
in the Valerianaceae. Biochem. Syst. Ecol. 26: 309–335.
Bell, C.D. 2004. Preliminary phylogeny of Valerianaceae (Dipsacales) inferred from nuclear and
chloroplast DNA sequence data. Mol. Phylogenet. Evol. 31: 340–350.
Bell, C.D. and Donoghue, M.J. 2005. Phylogeny and biogeography of Valerianaceae (Dipsacales) with
special reference to the South American valerians. Org. Divers. Evol. 5: 147–159.
Bell, C.D. 2007. Phylogenetic placement and biogeography of the North American species of Valerianella
(Valerianaceae: Dipsacales) based on chloroplast and nuclear DNA. Mol. Phylogenet. Evol.
44: 929–941.
Bell, C.D., Kutschker, A. and Arroyo, M.T.K. 2012. Phylogeny and diversification of Valerianaceae
(Dipsacales) in the southern Andes. Mol. Phylogenet. Evol. 63: 724–737. doi:10.1016/j.
ympev.2012.02.015.
Borsini, O.E. 1966. Valerianáceas de Chile. Lilloa 32: 375–476.
Borsini, O.E., Rossow, R.A. and Correa, M.N. 1999. Valerianaceae. pp. 449–468. In: Correa, M.N. (ed.).
Parte VI. Dicotyledones Gamopetalas. Flora Patagónica. Buenos Airess: INTA.
Bos, R., Woerdenbag, H.J., Hendriks, H., Smit, H.F., Wikström, H.V. and Scheffer, J.J. 1997. Composition
of the essential oil from roots and rhizomes of Valeriana wallichii DC. Flavour Frag. J. 12: 123–131.
Castillo García, E. and Martínez Solís, I. 2007. Manual de Fitoterapia. Elsevier, España, 536 pp.
Conticello, L., Gandullo, R., Bustamante, A. and Tartaglia, C. 1997. El uso de plantas medicinales por la
comunidad Mapuche de San Martín de los Andes, Provincia de Neuquén. Parodiana 10: 165–180.
Cuadra, P. and Fajardo, V. 2002. A new lignan from the Patagonian Valeriana carnosa Sm. Bol. Soc.
Chil. Quim. 47: 361–366.
Cuassolo, F. 2009. Estudio Etnobotánico de las plantas medicinales nativas y exóticas comercializadas
en la Ciudad de Bariloche, Patagonia, Argentina. Universidad Nacional del Comahue.
Cuassolo, F., Ladio, A.H. and Ezcurra, C. 2011. Aspectos de la comercialización y control de calidad de
las plantas medicinales más vendidas en una comunidad urbana del NO de la Patagonia Argentina.
Bol. Lat. y del Caribe, Pl. Medic. y Arom. 9: 166–176.
De Candolle, A.P. 1815. Flore française. V6. Paris.
Eriksen, B. 1989. Notes on generic and infrageneric delimitation in the Valerianaceae. Nordic J. Bot.
9: 179–187.
Estomba, D., Ladio, A.H. and Lozada, M. 2005. Plantas medicinales utilizadas por una comunidad
Mapuche en las cercanías de Junín de los Andes, Neuquén. Bol. Lat. y del Caribe, Pl. Medic. y
Arom. 4: 107–112.
Estomba, D., Ladio, A. and Lozada, M. 2006. Medicinal wild plant knowledge and gathering patterns
in a Mapuche community from North-western Patagonia. J. Ethnopharmacol. 103: 109–119.
doi:10.1016/j.jep.2005.07.015.
Fajardo, V., Gallardo, A., Araya, M., Joseph-Nathan, P., Oyarzún, A., Cuadra, P., Sanhueza, V.,
Manosalva, L., Villarroel, L. and Darias, J. 2010. Química y algunos antecedentes y ensayos
simples de la actividad biológica de plantas de la zona austral de chile. Dominguezia 26: 4–5.
Fernández, S., Wasowski, C., Paladini, A.C. and Marder, M. 2004. Sedative and sleep-enhancing
properties of linarin, a flavonoid-isolated from Valeriana officinalis. Pharmacol. Biochem. Behav.
77: 399–404.
100 ETHNOBOTANY: Local Knowledge and Traditions
Fernández, S., Wasowski, C., Paladini, A.C. and Marder, M. 2005. Synergistic interaction between
hesperidin, a natural flavonoid, and diazepam. Eur. J. Pharmacol. 512: 189–198.
Fernández, S., Wasowski, C., Loscalzo, L., Granger, R.E., Johnston, G.A.R., Paladini, A.C. and
Marder, M. 2006. Central nervous system depressant action of flavonoid glycosides. Eur. J.
Pharmacol. 539:168–176.
Ferreyra, M., Ezcurra, C. and Clayton, S. 2006. Flores de alta montaña de los Andes patagónicos. “High
Mountain Flora of the Patagonian Andes”. Editorial L.O.L.A., Buenos Aires.
Gratti A., Peneff, R. and Freile, M.L. 2010. Valeriana en la estepa patagonica, Argentina: Aportes al
conocimiento fitoquimico. Dominguezia 26: 19–20.
Grusla, D., Holzl, J. and Krieglstein, J. 1986. Effect of valerian on rat brain. Dtsch. Apoth. Ztg. 126:
2249–2253.
Guajardo, J., Gastaldi, B., González, S. and Nagahama, N. 2018. Variability of phenolic compounds
at different phenological stages in two populations of Valeriana carnosa Sm. (Valerianoideae,
Caprifoliaceae) in Patagonia. Bol. Lat. y del Caribe, Pl. Medic. y Arom. 17 (4): 381–393.
Gurib-Fakim, A. 2006. Medicinal plants: traditions of yesterday and drugs of tomorrow. Mol. Aspects
Med. 27: 1–93. doi:10.1016/j.mam.2005.07.008.
Hallam, K.T., Olver, J.S., McGrath, C. and Norman, T.R. 2003. Comparative cognitive and psychomotor
effects of single doses of Valeriana officinalis and triazolam in healthy volunteers. Hum.
Psychopharmacol. 18: 619–625.
Hattesohl, M., Feistel, B., Sievers, H., Lehnfeld, R., Hegger, M. and Winterhoff, H. 2008. Extracts
of Valeriana officinalis L. sl show anxiolytic and antidepressant effects but neither sedative nor
myorelaxant properties. Phytomedicine 15: 2–15.
Hidalgo, O., Garnatje, T., Susanna, A. and Mathez, J. 2004. Phylogeny of Valerianaceae based on matK
and ITS markers, with reference to matK individual polymorphism. Ann. Bot. 93: 283–293.
Holzmann, I., Cechinel Filho, V., Mora, T.C., Cáceres, A., Martínez, J.V., Cruz, S.M. and de Souza,
M.M. 2011. Evaluation of behavioral and pharmacological effects of hydroalcoholic extract of
Valeriana prionophylla Standl. from Guatemala. Evid. Based Complement. Alternat. Med. http://
dx.doi.org/10.1155/2011/312320.
http://www.anmat.gov.ar/webanmat/fna/fna.asp. 2013. Farmacopea Argentina. 7ed. Consultado:
Febrero de 2015.
Jugran, A., Rawat, S., Dauthal, P., Mondal, S., Bhatt, I.D. and Rawal, R.S. 2013. Association of ISSR
markers with some biochemical traits of Valeriana jatamansi Jones. Ind. Crops Prod. 44: 671–676.
Kutschker A., Menoyo, H. and Hechem, V. 2002. Plantas medicinales de uso popular encomunidades
del oeste del Chubut. Ed. Bavaria. INTA-UN de la Patagonia S.J.B.-GTZ, Bariloche.
Kutschker, A. 2011. Revisión del género Valeriana (Valerianaceae) en Sudamérica austral. Gayana
Bot. 68: 244–296.
Kutschker, A., Ezcurra, C. and Balzaretti, V. 2010. Valeriana (Valerianaceae) de los Andes australes:
biodiversidad y compuestos químicos. pp. 219–224. In: Pochettino, M.L., Ladio, A.H. and Arenas,
P.M. (eds.). Tradiciones y Transformaciones en Etnobotánica, La Plata: CYTED.
Kutschker, A. and Morrone, J.J. 2012. Distributional patterns of the species of Valeriana (Valerianaceae)
in southern South America. Pl. Syst. Evol. 298: 535–547.
Lacher, S.K., Mayer, R., Sichardt, K., Nieber, K. and Müller, C.E. 2007. Interaction of valerian extracts
of different polarity with adenosine receptors: Identification of isovaltrate as an inverse agonist
at A1 receptors. Biochem. Pharmacol. 73: 248–258.
Ladio, A. 2006. Gathering of wild plant foods with medicinal use in a Mapuche community of Northwest
Patagonia. pp. 297–321. In: Pieroni, A. and Price, L.L. (eds.). Eating and Healing: Traditional
Food… . USA: Harworth Press.
Ladio, A., Lozada, M. and Weigandt, M. 2007. Comparison of traditional wild plant knowledge between
aboriginal communities inhabiting arid and forest environments in Patagonia, Argentina. J. Arid
Environ. 69: 695–715. doi:10.1016/j.jaridenv.2006.11.008.
Ladio, A.H. and Lozada, M. 2009. Human ecology, ethnobotany and traditional practices in rural
populations inhabiting the Monte region: Resilience and ecological knowledge. J. Arid Environ.
73: 222–227. doi:10.1016/j.jaridenv.2008.02.006.
Ethnopharmacology and Ethnobotany of Valeriana carnosa 101
Marder, M., Violab, H., Wasowski, C., Fernández, S., Medinab, J.H. and Paladini, A.C. 2003.
6-Methylapigenin and hesperidin: new valeriana flavonoids with activity on the CNS. Pharmacol.
Biochem. Behav. 75: 537–545.
Martínez Crovetto, R. 1980. Apuntes sobre la vegetación de los alrededores del Lago Cholila. Publicación
Técnica de la Facultad de Ciencias Agrarias 1: 1–22.
Miller, P. 1754. The gardeners dictionary, abr. Self published, London. Vol. 3, 584 pp.
Molares, S. and Ladio, A. 2008. Plantas Medicinales en una comunidad mapuche del NO de la Patagonia
Argentina: clasificación y percepciones organolépticas relacionadas con su valoración. Bol. Lat.
y del Caribe, Pl. Medic. y Arom. 7(3): 149–155.
Molares, S. and Ladio, A. 2009a. Chemosensory perception and medicinal plants for digestive ailments
in a Mapuche community in NW Patagonia, Argentina. J. Ethnopharmacol. 123: 397–406.
doi:10.1016/j.jep.2009.03.033.
Molares, S. and Ladio, A. 2009b. Ethnobotanical review of the Mapuche medicinal flora: use patterns
on a regional scale. J. Ethnopharmacol. 122: 251–60. doi:10.1016/j.jep.2009.01.003.
Molares, S. 2010. Flora medicinal aromática de la Patagonia: características anatómicas y propiedades
organolépticas utilizadas en el reconocimiento por parte de la terapéutica popular. Tesis Doctoral.
Universidad Nacional del Comahue. Bariloche.
Molares, S. and Ladio, A.H. 2012. Plantas aromáticas con órganos subterráneos de importancia cultural
en la patagonia argentina: una aproximación a sus usos desde la etnobotánica, la percepción
sensorial y la anatomía. Darwiniana 50: 7–24.
Müller, L.G., Salles, L.A., Stein, A.C., Betti, A.H., Sakamoto, S., Cassel, E. and Rates, S.M. 2012.
Antidepressant-like effect of Valeriana glechomifolia Meyer (Valerianaceae) in mice. Prog.
Neuropsychopharmacol. Biol. Psychiatry 36: 101–109.
Murphy, K., Kubin, Z.J., Shepherd, J.N. and Ettinger, R. 2010. Valeriana officinalis root extracts have
potent anxiolytic effects in laboratory rats. Phytomedicine 17: 674–678.
Nagahama, N., Bach, H.G., Opazo, W., Miserendino, E., Arizio, C., Manifesto, M. and Fortunato, R.
2016. Aprovechamiento sustentable de recursos genéticos nativos: Valeriana carnosa Sm., estudio
de caso de una planta medicinal patagónica. Dominguezia 32: 68–69.
Nam, S.M., Choi, J.H., Yoo, D.Y., Kim, W., Jung, H.Y., Kim, J.W. and Yoon, Y.S. 2013. Valeriana
officinalis extract and its main component, valerenic acid, ameliorate D-galactose-induced
reductions in memory, cell proliferation, and neuroblast differentiation by reducing corticosterone
levels and lipid peroxidation. Exp. Gerontol. 48: 1369–1377.
Nahrstedt, A. 1984. Drugs and phytopharmaca having sedative activity. Dtsch. Apoth. Ztg. 124:
1213–1216.
Ochoa, J.J. and Ladio, A.H. 2011. Pasado y presente del uso de plantas silvestres con órganos de
almacenamiento subterráneos comestibles en la Patagonia. Bonplandia 20: 265–284.
Ochoa, J.J. and Ladio, A.H. 2014. Ethnoecology of Oxalis adenophylla Gillies ex Hook. & Arn. J.
Ethnopharmacol. 155: 533–542.
Oliva, I., González‐Trujano, M., Arrieta, J., Enciso‐Rodríguez, R. and Navarrete, A. 2004.
Neuropharmacological profile of hydroalcohol extract of Valeriana edulis ssp. procera roots in
mice. Phytother. Res. 18: 290–296.
Richeri, M., Cardoso, M.B. and Ladio, A.H. 2013. Soluciones locales y flexibilidad en el conocimiento
ecológico tradicional frente a procesos de cambio ambiental: estudios de caso en Patagonia.
Ecología Austral. (23): 184–193.
Sah, S.P., Mathela, C.S. and Chopra, K. 2011. Antidepressant effect of Valeriana wallichii patchouli
alcohol chemotype in mice: Behavioural and biochemical evidence. J. Ethnopharmacol. 135:
197–200.
Subhan, F., Karim, N., Gilani, A.H. and Sewell, R.D.E. 2010. Terpenoid content of Valeriana wallichii
extracts and antidepressant-like response profiles. Phytother. Res. 24: 686–91.
Surveswaran, S., Cai, Y.Z., Corke, H. and Sun, M. 2007. Systematic evaluation of natural phenolic
antioxidants from 133 Indian medicinal plants. Food Chem. 102: 938–953.
Thies, P.W. and Funke, S. 1966. Über die wirkstoffe des baldrians: 1. Mitteilung Nachweis und isolierung
von sedativ wirksamen isovaleriansäureestern aus wurzeln und rhizomen von verschiedenen
valeriana-und kentranthus-arten. Tetrahedron Letters 7: 1155–1162.
102 ETHNOBOTANY: Local Knowledge and Traditions
Toledo, C. and Kutschker, A. 2012. Plantas Medicinales en el Parque nacional los alerces, chubut,
Patagonia Argentina. Bol. Soc. Argent. Bot. 47: 461–470.
Upton, R., Petrone, C., Swisher, D., Goldberg, A., Mc Guffin, M. and Pizzorno, N.D.J. 1999. Valerian
Root Valeriana officinalis Analytical, Quality Control, and Therapeutic Monograph. Santa Cruz,
CA: American Herbal Pharmacopoeia (AHP).
Wagner, H., Jurcic, K. and Schaette, R. 1980. Comparative studies on the sedative action of Valeriana
extracts, valepotriates and their degradation products. Planta Med. 39: 358–365.
Weigandt, M., Ladio, A. and Lozada, M. 2004. Plantas medicinales utilizadas en la comunidad Mapuche
Curruhuinca. Ediciones Imaginaria. Bariloche. Argentina. 75 pp.
Zuloaga, F.O., Morrone, O. and Belgrano, J.M. 2008. Catálogo de las plantas vasculares del Cono Sur.
Monographs in systematic botany from the Missouri Botanical Garden. Ed. Missouri Botanical
Garden Press. http://www2.darwin.edu. ar.
CHAPTER 7
Traditional Knowledge of
Antivenom Plants
Bioactive Compounds and Their Antiophidic
Properties
Carolina Alves dos Santos,1,4 Marco V. Chaud,1,4 Valquíria Miwa
Hanai Yoshida,3 Raksha Pandit,2 Mahendra Rai2,* and
Yoko Oshima-Franco4
Introduction
The medicinal plants and their secondary metabolites are capable of promoting
different pharmacological and biological responses, and hence they are important
source of pharmaceuticals. In Brazil, natural and animal resources favour the study
and discovery of new plant activities, and hence the use of plants with antivenom
property is an interesting area of research. In developing countries, communities
in rural and urban areas are still heavily dependent on herbal medicines as primary
health care (Maroyi 2017). In tropical and subtropical countries, such as Africa,
Latin America, Asia and Oceania, snakebite poisoning is a real public health issue
(Gomes et al. 2016).
1
LaBNUS – Biomaterials and Nanotechnology Laboratory, University of Sorocaba, Sorocaba/SP,
Brazil.
2
Department of Biotechnology, SGB Amravati University, Amravati-444 602, Maharashtra, India.
3
Department of Technology & Environmental Process, University of Sorocaba UNISO, Sorocaba,
SP – Brazil.
4
Post Graduate Program in Pharmaceutical Sciences, Department of Development and Evaluation of
Bioactive Substances, University of Sorocaba, UNISO, Sorocaba, SP, Brazil.
* Corresponding author: [email protected]
104 ETHNOBOTANY: Local Knowledge and Traditions
Serum therapy is one of the measure for the treatment of poisoning caused
by snakebites. The main aim of serum therapy is that it can reverse the effects
of the complex and varied composition of substances and proteins present in the
venom. The pathophysiological process of poisoning involves toxins such as
metalloproteins, proteinases, phospholipases, hyaluronidases, pharmacological
enzymes and mediators (Gomes et al. 2016). Poisoning may result in different
degrees of toxicity such as neuroparalysis, multiple organ failure, and death (Naik
and Sadananda 2017). The pathophysiological effects induced by snake venom are
tissue necrosis, inhibition of platelet aggregation, hemorrhage, edema, etc. (Fig. 7.1).
Serum therapy consists of a mixture of antivenom antibodies isolated from
animals that aim to reverse the systemic effects of poisoning such as cardiac changes,
clotting disorders, renal and tissue damage, etc. (Félix-Silva et al. 2014). However,
serum therapy is often not able to reverse tissue damage caused by the venom such
as edema, injury, hemorrhage and necrosis. Such damages are very debilitating and
often generate permanent sequelae. Therefore, the strategies to reduce these toxic
effects are necessary, which can prevent the toxic effects associated with snake
venom. The neutralization of the local effects of venom is a frequent problem and
the use of therapeutic compounds is an alternative, which is capable of reversing
or minimizing tissue damage. In this context, the use of plants with antiophidic
properties is interesting which can be used in the treatment and it may enhance the
benefits obtained from serum therapy. The major disadvantages of serum therapy
is that it is toxic, costly and the accessibility limitations in rural regions and distant
urban centers (Tianyi et al. 2017).
The present chapter discusses about the significance of plants with antivenom
properties. A few therapies are known, which can be used in the treatment of snake
bites and the available therapies have many drawbacks. The secondary metabolites
present in traditionally used plants can be used against snake venom.
phospholipase A2 (CB)
and crotoxin
107
Eclipta prostrata (L.) L. Ethanol aerial parts extract; Crotalus durissus In vitro and in vivo Mors et al. 1989
Wedelolactone; sitosterol; terrificus
stigmasterol
Wedelolactone Crotalus viridis viridis; In vitro and in vivo Melo and Ownby 1999
Agkistrodon contortrix
laticinctus; CVV and
ACL PLA2-myotoxins
Aqueous extract/ Bothrops jararaca, In vitro and in vivo Melo et al. 1994
wedelolactone, stigmasterol, B. jararacussu,
sitosterol Lachesis muta and
myotoxins
Butanol extract of plant/ Calloselasma In vitro and in vivo Pithayanukul et al. 2004
demethylwedelolactone rhodostoma
Plant extract Gloydius brevicaudus, In vivo Chen et al. 2005
G. shedaoensis,
G. ussuriensis and
Deinagkistrodon acutus
Mikania laevigata Sch. Bip. Ethanol leaf extract Philodryas olfersii In vitro and ex vivo Collaço et al. 2012
ex Baker
Pluchea indica (L.) Less. Root extract/beta-sitosterol, Daboia russelli; In vitro and in vivo Gomes et al. 2007
stigmasterol Naja naja
Balanitaceae/ Balanites aegyptiaca (L.) Polarity-based stem barks Echis carinatus In vivo Wufem et al. 2007
Zygophyllaceae Del. extract
Seed oil Vipera russelli In vivo Mishal et al. 2014
Bignoniaceae Tabebuia rosea (Bertold.) Ethanol leaf and branches Bothrops asper In vitro and in vivo Nuñez et al. 2004
DC. extract
Bixaceae Bixa orellana L. Ethanol leaf and branches Bothrops asper In vitro and in vivo Nuñez et al. 2004
extract
Boraginaceae Argusia argentea (L.f.) Methanol extract/Rosmarinic Trimeresurus In vivo Aung et al. 2010
H. Heine acid flavoviridis;
Crotalus atrox,
Gloydius blomhoffii,
Bitis arietans and
mettalloproteinases
HT-b (C. atrox),
bilitoxin 2 (Agkistrodon
bilineatus), HF
(B. arietans), and
Ac1-proteinase
(Deinagkistrodon
Traditional Knowledge of Antivenom Plants
acutus)
Table 7.1 contd. …
109
…Table 7.1 contd.
Family Plant Part of plant used/bioactive Snake venoms/isolated Experimental References
compounds compounds design
Cordia verbanaceae DC. Methanol extract/Rosmarinic B. jararacussu venom In vitro and in vivo Ticli et al. 2005, Soares
acid and its basic PLA2s et al. 2005
Rosmarinic acid PrTX-I (Bothrops In vitro and ex vivo Santos et al. 2011
pirajai)
Burseraceae Boswellia dalzielli Hutch. Aqueous stem barks extract Naja nigricollis In vitro and in vivo Goje et al. 2013
Commiphora africana A. Methanol stem bark extract/ Naja nigricollis In vitro Isa et al. 2015
Rich. fractions
Caesalpiniaceae/ Bauhinia forficata Link. Aqueous aerial parts extract Bothrops jararacussu; In vitro Oliveira et al. 2005
Fabaceae (Fabaceae) B. moojeni; Crotalus
durissus terrificus and
PLA2s
Brownea rosademonte Berg. Ethanol leaf and branches Bothrops asper In vitro and in vivo Nuñez et al. 2004
extract
Combretaceae Combretum leprosum Mart. Root extract; Arjunolic acid Bothrops jararaca; In vitro and in vivo Fernandes et al. 2014
B. jararacussu
Combretum molle R. Br. ex Aqueous extract Bitis arietans; In vitro Molander et al. 2014
110 ETHNOBOTANY: Local Knowledge and Traditions
Euphorbiaceae Acalypha indica L. Ethanol leaf extract Vipera russelli russelli In vivo Shirwaikar et al. 2004
Table 7.1 contd. …
111
…Table 7.1 contd.
Family Plant Part of plant used/bioactive Snake venoms/isolated Experimental References
compounds compounds design
Bridelia ferruginea Benth. Ethanol leaf extract Naja nigricollis In vitro and in vivo Momoh et al. 2012.
Croton urucurana Baillon Aqueous extract/ Bothrops jararaca In vitro and in vivo Esmeraldino et al. 2005
proanthocyanidins
Emblica officinalis Linn. Methanol root extract Vipera russelli In vitro and in vivo Alam and Gomes 2003
Gaertn. Naja kaouthia
Root extract/Phtalate Naja Kaouthia; In vitro, ex vivo, in Sarkhel et al. 2011
compound Vipera russellii vivo
Jatropha elliptica (Pohl) Ethanol ryzomes extract Bothrops jararacussu In vitro and in vivo Ferreira-Rodrigues et
Oken. al. 2016
Jatropha gossypiifolia L. Aqueous leaf extract Bothrops jararaca In vitro and in vivo Felix-Silva et al. 2014
Jatropha mollissima (Pohl) Aqueous leaf extract Bothrops erythromelas; In vitro and in vivo Gomes et al. 2016
Bail B. jararaca
Dipteryx alata Vogel Polarity-based barks extracts Bothrops jararacussu; In vitro and ex vivo Nazato et al. 2010
Crotalus durissus
terrificus
Polarity-based barks fractions Bothrops jararacussu In vitro and ex vivo Puebla et al. 2010
112 ETHNOBOTANY: Local Knowledge and Traditions
Lupeol; lupenone; 28-OH- Bothrops jararacussu; In vitro and ex vivo Ferraz et al. 2012
lupenone; betulin Crotalus durissus
terrificus
7,8,3’-trihydroxy-4’- Bothrops jararacussu; In vitro and ex vivo Ferraz et al. 2014
methoxyisoflavone Bothropstoxin-I
(BthTX-I)
Betulin Bothrops jararacussu In vivo Ferraz et al. 2015
Protocatechuic acid; Vanillic In vitro and ex vivo Yoshida et al. 2015
acid; Vanillin
Erythrina senegalensis DC.
Mucuna pruriens (L.) DC Aqueous seed extract Family Elapidae In vitro and in vivo Tan et al. 2009
Ophiophagus hannah;
Naja sputatrix;
Bungarus candidus;
Notechis scutatus;
Pseudechis australis;
Family Viperidae
Trimeresurus
purpureomaculatus;
Naja nigricollis;
Bothrops asper;
Agkistrodon piscivorus;
Vipera russelli russelli .
Echis carinatus Guerranti et al. 2002
Guerranti et al. 2004
Pentaclethra Aqueous extract Bothrops jaracussu; In vitro and in vivo Da Silva et al. 2005
macroloba (Willd.) Kuntze B. atrox;
metalloproteases
Triterpenoid saponin B. neuwiedi; In vitro and in vivo Da Silva et al. 2007
inhibitors, named B. jararacussu;
macrolobin-A and B metlloproteases
Tamarindus indica L. Seed extract Vipera russelli In vitro and in vivo Ushanandini et al. 2006
Flacourtiaceae Casearia gossypiosperma Hexane leaf extract Bothrops jararacussu In vitro and ex vivo Soares-Silva et al. 2014
Briquet Hydroalcoholic leaf extract Camargo et al. 2010
Casearia sylvestris Sw. Aqueous leaf extract Bothrops moojeni; In vitro and in vivo Borges et al. 2000
B. jararacussu;
B. neuwiedi;
Crotalus durissus
Traditional Knowledge of Antivenom Plants
terrificus;
Micrurus frontalis
113
Lamiaceae Peltodon radicans Pohl. Polarity-based leaf, flowers Bothrops atrox In vitro and in vivo Costa et al. 2008
stem and barks extracts;
phytochemical isolated
Vitex negundo L. Methanol root extract Vipera russelli In vitro and in vivo Alam and Gomes 2003
Naja kaouthia
Leguminosae Brongniartia intermedia Isolated (-)-edunol from roots Bothrops atrox In vivo Reyes-Chilpa et al.
Moric.; B. podalyrioides 1994
Kunth.
Galactia glauscecens Kunth. Ethanol leaf extract Crotalus durissus In vitro and in vivo Dal Belo et al. 2008
terrificus
Loganiaceae Strychnos nux vomica L. Ethanol seed extract Daboia russelli; In vitro and in vivo Chatterjee et al. 2004
Naja kaouthia
Strychnos pseudoquina St. Methanol leaf extract Bothrops jararaca In vivo Nishijima et al. 2009
Hill.
Strychnos spinosa Lam. Aqueous stem bark extract Echis carinatus In vivo
Loranthaceae Struthanthus orbicularis Ethanol leaf and branches Bothrops asper In vitro and in vivo Nuñez et al. 2004
extract
Malpighiaceae Byrsonima crassa Niendezu Methanol leaf extract; Bothrops jararaca In vivo Nishijima et al. 2009
Amenthoflavone;
Quercetin
Malvaceae Hibiscus aethiopicus L. Aqueous whole plant extract Echis ocellatus; In vitro and in vivo Hasson et al. 2010
Naja n. nigricollis
Ethanol leaf and barks extract Echis carinatus In vivo Hasson et al. 2012
Sochureki
Hibiscus sabdariffa L.
Melastomataceae Bellucia dichotoma Cogn. Aqueous barks extract Bothrops atrox In vitro and in vivo Moura et al. 2014
Mouriri pusa Gardn. Methanol leaf extract; Bothrops jararaca In vivo Nishijima et al. 2009
Quercetin; Myricetin
Meliaceae Azadirachta indica A. Juss. Purified compound (AIPLAI) Naja naja; In vitro Mukherjee et al. 2008
from methanol leaf extract Naja kaouthia;
Daboia russelli
Mimosaceae Abarema cochliacarpos Hydroethanol stem barks Bothrops leucurus In vitro and in vivo Saturnino-Oliveira et
(Gomes) Barneby & extract al. 2014
J.W.Grimes
Traditional Knowledge of Antivenom Plants
Benth
Moraceae Ficus nymphaeifolia Miller Ethanol leaf and branches Bothrops asper In vitro and in vivo Nuñez et al. 2004
extract
Morus alba L. Leaf extract Daboia russelli In vitro and in vivo Chandrashekara et al.
2009
Musaceae Musa paradisíaca L. Exudates or juice from liberian Bothrops jararacussu; In vitro and in vivo Borges et al. 2005
vessels B. neuwiedi
Piperaceae Piper longum L. Ethanolic fruits extract/ Daboia russelli In vitro and in vivo Shenoy et al. 2013,
piperine 2014
Polygalaceae Securidada Aqueous leaf and root bark Naja nigricollis In vitro and in vivo Sanusi et al. 2014
longepedonculata Fresen.
Polypodiaceae Pleopeltis percussa (Cav.) Ethanol leaf and branches Bothrops asper In vitro and in vivo Nuñez et al. 2004
Hook & Grev. extract
Rubiaceae Gonzalagunia panamensis Ethanol leaf and branches Bothrops asper In vitro and in vivo Nuñez et al. 2004
(Cav.) Schumm. extract
Rutaceae Citrus limon L. Ethanol leaf and branches Bothrops asper In vitro and in vivo Nuñez et al. 2004
extract
Salicaceae Salix nigra Marshall Methanol leaf extract Bungarus sindarus In vitro Ahmed et al. 2016
Sapindaceae Sapindus saponaria L. Callus culture extracts Bothrops jararacussu; In vitro and in vivo da Silva et al. 2012
(polarity-based solvents) B. moojeni;
B.alternatus;
Crotalus durissus
terrificus;
Myotoxins and
phospholipases A2
Sapotaceae Manilkara subsericea Polarity-based leaf and stems Lachesis muta In vitro and in vivo De Oliveira et al. 2014
(Mart.) Dubard extracts
Solanaceae Whitania somnifera (L.) NN-XIa-PLA2 Naja naja In vitro, ex vivo, in Machiah and Gowda
Dunal vivo 2006
Theaceae Camellia sinensis Methanol leaf extract Naja naja In vitro and in vivo Pithayanukul et al. 2010
(L.) Kuntze kaouthia Lesson
(Elapidae);
Calloselasma
rhodostoma Kuhl
(Viperidae)
Hydroalcohol leaf extract; Crotalus durissus In vitro and ex vivo de Jesus Reis Rosa et
theaflavin and epigallocatechin terrificus al. 2010
Hydroalcohol leaf extract Bothrops jararacussu; In vitro and ex vivo Oshima-Franco et al.
Bothropstoxin-I 2012
(BthTX-I)
Traditional Knowledge of Antivenom Plants
based solventes)/
ar-turmerone
Aqueous extract Naja naja sinensis In vitro and ex vivo Daduang et al. 2005
Aqueous-isopropanol green Bothrops alternatus In vitro and in vivo Melo et al. 2007
leaves extract
Curcuma sp. Aqueous extract Naja naja siamensis In vitro Cherdchu and Karlsson
1983
Curcuma parviflora Wall. Aqueous extract Naja naja sianensis In vitro and ex vivo Daduang et al. 2005
Renealmia alpinia (Rottb.) Ethanol leaf and branches Bothrops asper In vitro and in vivo Nuñez et al. 2004
extract
Traditional Knowledge of Antivenom Plants 119
Table 7.2. Some examples of plants with antiophidic properties with mechanism of inhibition.
this study, three alkaloids were isolated and characterized. The results showed that
alkaloids studied could inhibit myotoxicity of B. pauloensis by inhibition of Asp49
activity. For antihemorrhagic and antinecrotizing activity, the hemorrhage provoque
by venom are clearly decreased when alkaloid 1 and 2 are previously administered.
The necrotic effect was also affected by alkaloid 1 and 2 administration. Authors
also emphasized that snake venom metalloproteases (SVMP) is the main toxin
responsible for hemorrhagic and necrosis and the antihemorrhagic and antinecrosis
properties found in alkaloids 1 and 2 are due to the capacity of these compounds
to interact with metals and metalloproteases.
Silva et al. (2007) studied the capacity of plants’ mixture used in indigenous
medicinal practice in Sri Lanka against venom toxins of Naja naja and Daboia
russelii (Russell’s viper). These plants mixture was composed by Sansevieria
Traditional Knowledge of Antivenom Plants 121
cylindrica, Jatropha podagrica and Citrus aurantiifolia. The study was performed
by evaluation of the potential of herbal mixture which inhibits venom toxicity in
chicken embryo model. The results showed the potential of herbal mixture that
neutralizes action of D. russeli venom. In the presence of herbal mixture, the
activity of phospholipase A2 (PLA2), of Daboia russelii venom was reduced from
9.2 103 mM min–1 to 8.0 103 mM min–1 and from N. naja from 2.92 102 mM min–1 to
0.188 × 10–2 mM min–1. With Naja venom, herbal mixture was also able to reduce
metalloprotease activity. Shabbir et al. (2014) reported that the main components
involved in neutralization properties against venom of snakes (Naja species)
include lupeol acetate, β-sitosterol, stigmasterol, rediocides A and G, quercertin,
aristolochic acid, and curcumin, as well as the broad chemical groups of tannins,
glycoproteins, and flavones. The authors emphazise that the chemical compounds of
plants enhance the survival of snakebite victims by decreasing the severity of toxins,
protect cardiovascular system, and enhance diaphragm contraction and others.
Khrishnan et al. (2013) studied the capacity of Ophiorrhiza mungos root
extact that neutralizes the venom of Daboia russelii snake. The neutralization/
inhibition of venom-induced lethality or hemorrhage was achieved by incubating
venom in chick embryo. The results showed 100% recovery of embryos with
10 mg/mL of extract which was effective in neutralizing the hemorrhage induced by
viper. Extracts of Ophiorrhiza mungos revealed the presence of terpenes, phenols,
flavonoids, alkaloids, quinones, tannins, glycosides and saponins.
Nazato et al. (2010) evaluated the antiophidian properties of Dipteryx alata
Vogel bark extract against Bothrops jararacussu and Crotalus durissus terrificus
snake venom. Authors reported the neurotoxic and myotoxic inhibition of
methanolic extracts against Bothrops jararacussu relating this inhibitory capacity
with the presence of phenolic acids and flavonoids contained in the methanolic
extract plus tannins, terpenoids from dicloromethane extract seems to play an
important role in Bothrops jararacussu and Crotalus durissus terrificus. Important
observations discussed in this study are related with the potential of some extract
that do not inhibit venom from different species or even for the same species, a
fact that makes use of “antiophidic plant” many times premature. Consequently,
the antivenom activity of plants also depend on bioactive compounds and venom
pharmacology.
Main classes of PLA2 inhibitors are the phenolic compounds, which include
flavonoids, coumestans and alkaloids, steroids and terpenoids (mono-, di-, and
triterpenes), and polyphenols (vegetable tannins) (Carvalho et al. 2013).
Identification of bioactive compounds present in plants extracts can be
performed using analytical techniques that allow identifying the profiles and
elucidating molecular characteristics of the main compounds enrolled in antivenom
activity.
Liu et al. (2015) reported the use of high-performance liquid chromatography,
high-resolution mass spectrometry, solid-phase extraction and nuclear magnetic
resonance spectroscopy (HPLC–HRMS–SPE–NMR). These techniques were used
122 ETHNOBOTANY: Local Knowledge and Traditions
References
Abubakar, M.S., Sule, M.I., Pateh, U.U., Abdurahman, E.M., Haruna, A.K. and Jahun, B.M. 2000.
In vitro snake venom detoxifying action of the leaf extract of Guiera senegalensis. J.
Ethnopharmacol. 69(3): 253–257.
Adzu, B., Abubakar, M.S., Izebe, K.S., Akumka, D.D. and Gamaniel, K.S. 2005. Effect of Annona
senegalensis rootbark extracts on Naja nigricotlis nigricotlis venom in rats. J. Ethnopharmacol.
96(3): 507–513.
Traditional Knowledge of Antivenom Plants 123
Ahmed, A., Rajendaran, D., Jaiswal, D., Singh, H.P., Mishra, A., Chandra, D., Yadav, I.K. and Jain,
D.A. 2010. Anti-snake venom activity of different extracts of Pouzolzia indica against russel viper
venom. Int. J. ChemTech Res. 2(1): 744–751.
Ahmed, W., Ahmad, M., Khan, R.A. and Mustaq, N. 2016. Promising inhibition of krait snake’s venom
acetylcholinesterase by Salix nigra and its role as anticancer, antioxidante agent. Indian J. Anim.
Res. 50(3): 317–323.
Alam, M.I., Auddy, B. and Gomes, A. 1994. Isolation, purification and partial characterization of viper
venom inhibiting factor from the root extract of the Indian medicinal plant sarsaparilla (Hemidesmus
indicus R. Br.). Toxicon 32(12): 1551–1557.
Alam, M.I. and Gomes, A. 1998. Adjuvant effects and antiserum action potentiation by a (herbal)
compound 2-hydroxy-4-methoxy benzoic acid isolated from the root extract of the Indian medicinal
plant “sarsaparilla” (Hemidesmus indicus R. Br.). Toxicon 36(10): 1423–1431.
Alam, M.I. and Gomes, A. 1998. Viper venom-induced inflammation and inhibition of free radical
formation by pure compound (2-hydroxy-4-methoxy benzoic acid) isolated and purified from
anantamul (Hemidesmus indicus R.Br) root extract. Toxicon 36(1): 207–215.
Alam, M.I. and Gomes, A. 2003. Snake venom neutralization by Indian medicinal plants (Vitex negundo
and Emblica officinalis) root extracts. J. Ethnopharmacol. 86: 75–80.
Ambikabothy, J., Ibrahim, H., Ambu, S., Chakravarthi, S., Awang, K. and Vejayan, J. 2011. Efficacy
evaluations of Mimosa pudica tannin isolate (MPT) for its anti-ophidian properties. J.
Ethnopharmacol. 137(1): 257–262.
Assafim, M., de Coriolano, E.C., Benedito, S.E., Fernandes, C.P., Lobo, J.F.R., Sanchez, E.F., Rocha,
L.M. and Lopes, A. 2011. Hypericum brasiliense plant extract neutralizes some biological effects
of Bothrops jararaca snake venom. J. Venom Res. 2: 11–16.
Aung, H.T., Nikai, T., Niwa, M. and Takaya, Y. 2010. Rosmarinic acid in Argusia argentea inhibits
snake venom-induced hemorrhage. J. Nat. Med. 64(4): 482–486.
Batina, M., De, F., Cintra, A.C., Veronese, E.L., Lavrador, M.A., Giglio J.R., Pereira, O.S., Dias, D.A.,
França, S.C. and Sampaio, S.V. 2000. Inhibition of the lethal and myotoxic activities of Crotalus
Durissus Terrificus Venom By Tabernaemontana Catharinensis: Identification of one of the active
components. Planta Med. 66(5): 424–428.
Barma, A.D., Mohanty, J.P. and Bhuyan, N.R. 2014. A review on anti-venom activity of some medicinal
plants. IJPSR 5(5): 1612–1615.
Bhattacharjee, P. and Bhattacharyya, D. 2013. Characterization of the aqueous extract of the root
of Aristolochia indica: evaluation of its traditional use as an antidote for snake bites. J.
Ethnopharmacol. 145(1): 220–226.
Biondo, R., Pereira, A.M., Marcussi, S., Pereira, O.S., França, S.C. and Soares, A.M. 2003. Inhibition
of enzymatic and pharmacological activities of some snake venoms and toxins by Mandevilla
velutina (Apocynaceae) aqueous extract. Biochimie. 85(10): 1017–1025.
Biondo, R., Soares, A.M., Bertoni, B.W., França, S.C. and Pereira, M.A.S. 2004. Direct organogenesis
of Mandevilla illustris (Vell) Woodson and effects of its aqueous extract on the enzymatic and
toxic activities of Crotalus durissus terrificus snake venom. Plant Cell. Rep. 22(8): 549–552.
Borges, M.H., Soares, A.M., Rodrigues, V.M., Andrão-Escarso, S.H., Diniz, H., Hamaguchi, A., Quintero,
A., Lizano, S., Gutiérrez, J.M., Giglio, J.R. and Homsi-Brandeburgo, M.I. 2000. Effects of aqueous
extract of Casearia sylvestris (Flacourtiaceae) on actions of snake and bee venoms ando n activity
of phspholipases A2. Comp. Biochem. Physiol. Part B 127: 21–30.
Borges, M.H., Soares, A.M., Rodrigues, V.M., Oliveira, F., Frannsheschi, A.M., Rucavado, A., Giglio,
J.R. and Homsi-Brandeburgo, M.I. 2001. Neutralization of proteases from Bothrops snake venoms
by the aqueous extract from Casearia sylvestris (Flacourtiaceae). Toxicon 39: 1863–1869.
Borges, M.H., Alves, D.L.F., Raslan D.S., Piló-Veloso, D., Rodrigues, V.M., Homsi-Brandeburgo,
M.I. and de Lima, M.E. 2005. Neutralizing properties of Musa paradisíaca L. (Musaceae) juice
on phospholipase A2, myotoxic, hemorrhagic and lethal activities of crotalidade venoms. J.
Ethnopharmacol. 98: 21–29.
Camargo, T.M., Nazato, V.S., Silva, M.G., Cogo, J.C., Groppo, F.C. and Oshima-Franco, Y.
2010. Bothrops jararacussu venom-induced neuromuscular blockade inhibited by Casearia
124 ETHNOBOTANY: Local Knowledge and Traditions
gossypiosperma Briquet hydroalcoholic extract. J. Venom Anim. Toxins Incl. Trop. Dis. 16(3):
432–441.
Carvalho, B.M.A., Santos, J.D.L., Xavier, B.M., Almeida, J.R., Resende, L.M., Martins, W., Marcussi,
S., Marangoni, S., Stábeli, R.G., Calderon, L.A., Soares, A.M., Silva, S.L. and Marchi-Salvador,
D.P. 2013. Snake venom PLA2s inhibitors isolated from Brazilian plants: synthetic and natural
molecules. BioMed. Res. Int. (ID 153045): 8.
Cavalcante, W.L.G., Campos, T.O., Dal, Pai-Silva, M., Pereira, P.S., Oliveira, C.Z., Soares, A.M. and
Gallacci, M. 2007. Neutralization of snake venom phospholipase A2 toxins by aqueous extract
of Casearia sylvestris (Flacourtiaceae) in mouse neuromuscular preparation. J. Ethnopharmacol.
112(3): 490–497.
Chacko, N., Ibrahim, M., Shetty, P. and Shastry, C.S. 2012. Evaluation of antivenom activity of Calotropis
gigantea plant extract against Vipera russelli snake venom. IJPSR 3(7): 2272–2279.
Chandrashekara, K.T., Nagaraju, S., Nandini, S.U., Basavaiah and Kemparaju, K. 2009. Neutralization of
local and systemic toxicity of Daboia russelli venom by Morus alba plant leaf extract. Phytother.
Res. 23(8): 1082–1087.
Chatterjee, I., Chakravarty, A.K. and Gomes, A. 2004. Antisnake venom activity of ethanolic seed
extract of Strychnos nux vomica Linn. Indian J. Exp. Biol. 42(5): 468–475.
Chatterjee, I., Chakravarty, A.K. and Gomes, A. 2006. Daboia Russellii and Naja Kaouthia venom
neutralization by lupeol acetate isolated from the root extract of indian sarsaparilla Hemidesmus
Indicus R.Br. J. Ethnopharmacol. 106(1): 38–43.
Chen, J.J., Shi, D.J., Li, K.H., Liu, G.F. and Wang, Q.C. 2005. Effect of Ecliptaprostrate on inflammation
and hemorrhage induced by the snake venom. J. Snake 17(2): 65–68.
Cherdchu, C. and Karlsson, E. 1983. Proteolytic-independent cobra neurotoxin inhibiting activity
of Curcuma sp. (Zingiberaceae). Southeast Asian J. Trop. Med. Public Health 14(2): 176–180.
Chippaux, J.P., Rakotonirina, V.S., Rakotonirina, A. and Dzikouk, G. 1997. Drug or plant substances
which antagonize venoms or potentiate antivenins. Bull. Soc. Pathol. Exot. 90(4): 282–285.
Chippaux, J.P. 2017. Incidence and mortality due to snakebite in the Americas. Plos Negl. Trop. Dis.
11(6): e0005662. DOI: 10.1371/journal.pntd.0005662.
Cintra-Francischinelli, M., Silva, M.G., Andréo-Filho, N., Gerenutti, M., Cintra, A.C., Giglio, J.R., Leite,
G.B., Cruz-Höfling, M.A., Rodrigues-Simioni, L. and Oshima-Franco, Y. 2008. Antibothropic
action of Casearia sylvestris Sw. (Flacourtiaceae) extracts. Phytother. Res. 22(6): 784–790.
Collaço R de, C., Cogo, J.C., Rodrigues-Simioni, L., Rocha, T., Oshima-Franco, Y. and Randazzo-Moura,
P. 2012. Protection by Mikania laevigata (guaco) extract against the toxicity of Philodryas olfersii
snake venom. Toxicon. 60(4): 614–622.
Corbett, B. and Clark, R.F. 2017. North American snake envenomation. Emerg. Med. Clin. North Am.
35(2): 339–354.
Costa, H.N.R., Santos, M.C., Alcântara, A.F.C., Silva, M.C., França, R.C. and Piló-Veloso, D. 2008.
Chemical constituents and antiedematogenic activity of Peltodon radicans (Lamiaceae). Quím
Nova 31(4): 744–750.
da Silva, J.O., Coppede, J.S., Fernandes, V.C., Sant’ana, C.D., Ticli, F.K., Mazzi, M.V., Giglio, J.R.,
Pereira, P.S., Soares, A.M. and Sampaio, S.V. 2005. Antihemorrhagic, antinucleolytic and other
antiophidian properties of the aqueous extract from Pentaclethra macroloba. J. Ethnopharmacol.
100(1-2): 145–152.
Da Silva, J.O., Fernandes, R.S., Ticli, F.K., Oliveira, C.Z., Mazzi, M.V., Franco, J.J., Giuliatti, S., Pereira,
O.S., Soares, A.M. and Sampaio, S.V. 2007. Triterpenoids saponins, new metalloprotease snake
venom inhibitors isolated from Pentaclethra macroloba. Toxicon. 50(2): 283–291.
Da Silva, M.L., Marcussi, S., Fernandes, R.S., Pereira, P.S., Januário, A.H., França, S.C., Da Silva,
S.L., Soares, A.M. and Lourenço, M.V. 2012. Anti-snake venom activities of extracts and fractions
from callus cultures of Sapindus saponaria. Pharm. Biol. 50(3): 366–375.
da Silva, J.O., Fernandes, R.S., Ticli, F.K., Oliveira, C.Z., Mazzi, M.V., Franco, J.J., Giuliatti, S., Pereira,
P.S., Soares, A.M. and Sampaio, S.V. 2007. Triterpenoid saponins, new metalloprotease snake
venom inhibitors isolated from Pentaclethra macroloba. Toxicon 50(2): 283–291.
Traditional Knowledge of Antivenom Plants 125
Daduang, S., Sattayasai, N., Sattayasai, J., Tophrom, P., Thammathaworn, A., Chav eerach, A. and
Konkchaiyaphum, M. 2005. Screening of plants containing Naja naja siamensis cobra venom
inhibitory activity using modified Elisa technique. Anal. Biochem. 341(2): 316–325.
Dal Belo, C.A., Colares, A.V., Leite, G.B., Ticli, F.K., Sampaio, S.V., Cintra, A.C., Rodrigues-Simioni,
L. and dos Santos, M.G. 2008. Antineurotoxic activity of Galactia glaucescens against Crotalus
durissus terrificus venom. Fitoterapia 79(5): 378–80.
Dal Belo, C.A., Lucho, A.P.B., Vinadé, L., Rocha, L., França, H.S., Marangoni, S., Rodrigues-Simioni,
L. 2013. In vitro antiophidian mechanisms of Hypericum brasiliense Choisy standardized extract:
quercetin-dependent neuroprotection. BioMed. Res. Int. 943520: DOI: 10.1155/2013/943520.
De Almeida, L., Cintra, A.C., Veronese, E.L., Nomizo, A., Franco, J.J., Arantes, E.C., Giglio, J.R. and
Sampaio, S.V. 2004. Anticrotalic and antitumoral activities of gel filtration fractions of aqueous
extract from Tabernaemontana catharinensis (Apocynaceae). Comp. Biochem. Physiol. C Toxicol.
Pharmacol. 137(1): 19–27.
De Jesus Reis Rosa, L., Silva, G.A., Filho, J.A., Silva, M.G., Cogo, J.C., Groppo, F.C. and
Oshima-Franco, Y. 2010. The inhibitory effect of Camellia sinensis extracts against the
neuromuscular blockade of Crotalus durissus terrificus venom. J. Venom Res. 1: 1–7.
De Oliveira, E.C., Fernandes, C.P., Sanchez, E.F., Rocha, L. and Lopes, A. 2014. Inhibitory effect of
plant Manilkara subsericea against biological activities of Lachesis muta snake venom. BioMed.
Res. Int. 2014: Article ID 408068, 7 pages.
Dey, A. and De, J.N. 2012. Phytopharmacology of antiophidian botanicals: a review. Int. J. Pharmacol.
8(2): 62–79.
Dhananjaya, B.L. and Shivalingaiah, S. 2016. The anti-inflammatory activity of standard aqueous
stem bark extract of Mangifera indica L. as evident in inhibition of Group IA sPLA2. Ann. Braz.
Acad. Sci. 88(1): 197–209.
Dhananjaya, B.L., Sudarshan, S., Dongol, Y. and More, S.S. 2016. The standard aqueous stem bark
extract of Mangifera indica L. inhibits toxic PLA2 – NN-XIb-PLA2 of Indian cobra venom.
Saudi Pharm. J. 24(3): 371–378.
Diogo, L.C., Fernandes, R.S., Marcussi, S., Menaldo, D.L., Roberto, P.G., Matrangulo, P.V., Pereira,
P.S., França, S.C., Giuliatti, S., Soares, A.M. and Lourenço, M.V. 2009. Inhibition of snake venoms
and phospholipases A (2) by extracts from native and genetically modified Eclipta Alba: Isolation
of active coumestans. Basic Clin. Pharmacol. Toxicol. 104(4): 293–299.
Domingos, T.F.S., Vallim, M.A., Carvalho, C., Sanchez, E.F., Teixeira, V.L. and Fuly, A.L. 2011.
Anti-snake venom effect of secodolastane diterpenes isolated from Brazilian marine brown alga
Canistrocarpus cervicornis against Lachesis muta venom. Revista Brasileira de Farmacognosia
21(2): 234–238.
Emmanuel, N. and Mamoudou. 2015. Some investigations on the traditional Pharmacopoeia about
venomous bite and stings from Scorpions, snakes and spiders, in the Hina subdivision, Far-North
Cameroon. British J. Pharma. Res. 5(5): 344–358.
Esmeraldino, L.E., Souza, A.M. and Sampaio, S.V. 2005. Evaluation of the effect of aqueous extract of
Croton urucurana Bailon (Euphorbiaceae) on the hemorrhagic activity induced by the venom of
Bothrops jararaca using new techniques to quantify hemorrhagic activity in rat skin. Phytomed.
12(8): 570–576.
Farrapo, N.M., Silva, G.A.A., Costa, K.N., Silva, M.G., Cogo, J.C., Dal Belo, C.A., dos Santos, M.G.,
Groppo, F.C. and Oshima-Franco, Y. 2011. Inhibition of Bothrops jararacussu venom activities
by Plathymenia reticulata Benth extracts. J. Venom Res. 2: 52–58.
Feitosa, E.S., Sampaio, V., Sachett, J.,Castro, D.B., Noronha, M.D.N., Lozano, J.L.L, Muniz, E., Ferreira,
L.C.L Lacerda, M.V.G. and Monteiro, W.M. 2013. Snakebites as a largely neglected problem in
the Brazilian Amazon: highlights of the epidemiological trends in the State of Amazonas. http://
dx.doi.org/10.1590/0037-8682-0105-2015.
Félix-Silva, J., Souza, T., Menezes, Y.A., Cabral, B., Câmara, R.B., Silva-Junior, A.A., Rocha, H.A.,
Rebecchi, I.M., Zucolotto, S.M. and Fernandes-Pedrosa, M.F. 2014. Aqueous leaf extract of
Jatropha gossypiifolia L. (Euphorbiaceae) inhibits enzymatic and biological actions of Bothrops
jararaca snake venom. PLoS One 9(8): e104952. DOI: 10.1371/journal.pone.0104952.
126 ETHNOBOTANY: Local Knowledge and Traditions
Fernandes, J., Félix-Silva, J., Cunha, L., Gomes, A., Siqueira, M., Gimenes, L., Lopes, N., Soares, L.,
Fernandes-Pedrosa, M. and Zucolotto, S. 2016. Inhibitory effects of hydroethanolic leaf extracts
of Kalanchoe brasiliensis and Kalanchoe pinnata (Crassulaceae) against local effects induced
by Bothrops jararaca snake venom. PLoS One 11(12): e0172598.
Fernandes, F.F., Tomaz, M.A., El-Kik, C.Z., Monteiro-Machado, M., Strauch, M.A., Cons, B.L., Tavares-
Henriques, M.S., Cintra, A.C., Facundo, V.A. and Melo, P.A. 2014. Counteraction of Bothrops
snake venoms by Combretum leprosum root extract and arjunolic acid. J. Ethnopharmacol.
155(1): 552–562.
Ferraz, M.C., Parrilha, L.A.C., Moraes, M.S.D., Amaral Filho, J., Cogo, J.C., dos Santos, M.G., Franco,
L.M., Groppo, J.C., Puebla, P., San Feliciano, P. and Oshima-Franco, Y. 2012. The effect of lupane
triterpenoids (Dipteryx alata Vogel) in the in vitro neuromusuclar blockade and myotoxicity of
two snake venoms. Curr. Org. Chem. 16(22): 2717–2723.
Ferraz, M.C., Yoshida, E.H., Tavares, R.V., Cogo, J.C., Cintra, A.C., Dal Belo, C.A., Franco, L.M.,
dos Santos, M.G., Resende, F.A., Varanda, E.A., Hyslop, S., Puebla, P., San Feliciano, A. and
Oshima-Franco, Y. 2014. An isoflavone from Dipteryx alata Vogel is active against the in vitro
neuromuscular paralysis of Bothrops jararacussu snake venom and bothropstoxin-I, and prevents
venom-induces myonecrosis. Molecules 19(5): 5790–5805.
Ferraz, M.C., de Oliveira, J.L., de Oliveira, J.R., Cogo, J.C., dos Santos, M.G., Franco, L.M., Puebla, P.,
Ferraz, H.O., Ferraz, H.G., da Rocha, M.M., Hyslop, S., San Feliciano, A. and Oshima-Franco, Y.
2015. The tripernoid betulin protects against the neuromuscular effects of Bothrops jararacussu
snake venom in vivo. Evid. Based Complement Alternat. Med. 939523.
Ferreira, L.A., Henriques, O.B., Andreoni, A.A., Vital, G.R., Campos, M.M., Habermehl, G.G. and
de Moraes, V.L. 1992. Antivenom and biological effects of ar-turmerone isolated from Curcuma
longa (Zingiberaceae). Toxicon 30(10): 1211–1218.
Ferreira-Rodrigues, S.C., Rodrigues, C.M., Dos Santos, M.G., Gautuz, J.A., Silva, M.G., Cogo, J.C.,
Batista-Silva, C., Dos Santos, C.P., Groppo, F.C., Cogo-Müller, K. and Oshima-Franco, Y. 2016.
Anti-inflammatory and antibothropic properties of Jatropha elliptica, a plant from Brazilian
Cerrado Biome. Adv. Pharm. Bull. (4): 573–579.
Goje, L.J., Aisami, A., Maigari, F.U., Ghamba, P.E., Shuaibu, I. and Goji, A.D.T. 2013. The Anti snake
venom effects of the aqueous extracts of Boswellia delzielli stem bark on the parameters of hepatic
functions and energy metabolism of Naja nigricollis (Spitting Cobra) envenomed albino rats. Res.
J. Chem. Env. Sci. 1(4): 61–68.
Gomes, A., Saha, A., Chatterjee, I. and Chakravarty, A.K. 2007. Viper and cobra venom neutralization by
beta-sitosterol and stigmasterol isolated from the root extract of Pluchea indica Less. (Asteraceae).
Phytomedicine 14(9): 637–643.
Gomes, J.A., Félix-Silva, J., Morais Fernandes, J., Geraldo Amaral, J., Lopes, N.P., Tabosa do Egito,
E.S., da Silva-Júnior, A.A., Maria Zucolotto, S. and Fernandes-Pedrosa, M.F. 2016. Aqueous leaf
extract of Jatropha mollissima (Pohl) Bail decreases local effects Induced by bothropic venom.
Biomed. Res. Int. 6101742.
Gopi, K., Renu, K., Raj, M., Kumar, D. and Muthuvelan, B. 2011. The neutralization effect of methanol
extract of Andrographis paniculata on Indian cobra Naja naja snake venom. J. Pharm. Res.
4(4): 1010–1012.
Guerranti, R., Aguiyi, J.C., Neri, S., Leoncini, R., Pagani, R. and Marinello, E. 2002. Proteins from
Mucuna pruriens and enzymes from Echis carinatus venom: characterization and cross-reactions.
J. Biol. Chem. 277(19): 17072–17078.
Guerranti, R., Aguiyid, J.C., Oguelia, I.G., Onoratia, G., Neria, S., Rosatib, F., Del Buonob, F.,
Lamparielloc, R., Pagania, R. and Marinello, E. 2004. Protection of Mucuna pruriens seeds against
Echis carinatus venom is exerted through a multiform glycoprotein whose oligosaccharide chains
are functional in this role. Biochem. Biophys. Res. Comm. 323: 484–490.
Hasson, S.S., Al-Jabri, A.A., Sallam, T.A., Al-Balushi, M.S. and Mothana, R.A.A. 2010. Antisnake
venom activity of Hibiscus aethiopicus L. against Echis ocellatus and Naja n. nigricollis. J.
Toxicol. 2010: Article ID 837864, doi: 10.1155/2010/837864.
Hasson, S.S., Al-Balushi, M.S., Said, E.A., Habbal, O., Idris, M.A., Mothana, R.A.A., Sallam, T.A.
and Al-Jabri, A.A. 2012. Neutralisation of local haemorrhage induced by the saw-scaled viper
Traditional Knowledge of Antivenom Plants 127
Echis carinatus sochureki venom using ethanolic extract of Hibiscus aethiopicus L. Evid. Based
Complement Alternat. Med. 2012: Article ID 540671, 8 pages doi: 10.1155/2012/540671.
Hung, Y.C., Sava, V., Hong, M.Y. and Huang, G.S. 2004. Inhibitory effects on phospholipase A2 and
antivenin activity of melanin extracted from Thea sinensis Linn. Life Sci. 74(2004): 2037–2047.
Isa, H.I., Ambali, S.F., Suleiman, M.M., Abubakar, M.S., Kawu, U.M., Shittu, M., Yusuf, P.O. and
Habibu, B. 2015. In vitro neutralization of Naja nigricollis venom by stem-bark extracts of
Commiphora africana A. Rich. (Burseraceae). IOSR J. Environ Sci. Toxicol. Food Technol.
9(12): 100–105.
Kadali, V.N., Kameswara, R.K. and Sandeep, B.V. 2015. Medicinal plants with anti-snake venom
property—a review. Pharma Innov. J. 4(7): 11–15.
Krishnan, S.A., Dileepkumar, R., Nair, A.S. and Oommen, O.V. 2013. Studies on neutralizing effect
of Ophiorrhiza mungos root extract against Daboia russelii venom. http://dx.doi.org/10.1016/j.
jep.2013.11.010.
Leanpolchareanchai, J., Pithayanukul, P., Bavovada, R. and Saparpakorn, P. 2009. Molecular docking
studies and anti-enzymatic activity of Thai mango seed kernel extract against snake venoms.
Molecules 14(4): 1404–1422.
Li, C.M., Zhang, Y., Yang, J., Zou, B., Dong, X.Q. and Hagerman, A.E. 2013. The interaction of
persimmon proanthocyanidin fraction with Chinese cobra PLA2 and BSA. Toxicon. 67: 71–79.
Liu, Y., Staerk, D., Nielsen, M.N., Nyberg, N. and Jäger, A.K. 2015. High-resolution hyaluronidase
inhibition profiling combined with HPLC–HRMS–SPE–NMR for identification of anti-necrosis
constituents in Chinese plants used to treat snakebite. Phytochem. 112: 62–69.
Lobo, R., Punitha, I.S.R., Rajendran, K., Shirwaikar, A. and Shirwaikar, A. 2006. Preliminary study
on the anti-snake venom activity of alcoholic root extract of Clerodendrum viscosum (Vent.) in
Naja naja venom. Nat. Prod. Sci. 12(3): 153–156.
Machiah, D.K. and Gowda, T.V. 2006. Purification of a post-synaptic neurotoxic phospholipase A2
from Naja naja venom and its inhibition by a glycoprotein from Withania somnifera. Biochimie
88(6): 701–710.
Mahadeswaraswamy, Y.H., Devaraja, S., Kumar, M.S., Goutham, Y.N. and Kemparaju, K. 2009.
Inhibition of local effects of Indian Daboia/Vipera russelli venom by the methanolic extract of
grape (Vitis vinifera L.) seeds. Indian J. Biochem. Biophys. 46(2): 154–160.
Mahanta, M. and Mukherjee, A.K. 2001. Neutralization of lethality, myotoxicity and toxic enzymes of
Naja kaouthia venom by Mimosa pudica root extracts. J. Ethnopharmacol. 75: 55–60.
Maroyi, A. 2017. Kirkia Acuminata oliv.: a review of its ethnobotany and pharmacology. Afr. J. tradit.
complement Altern. Med. 14(2): 217–226.
Meenatchisundaram, S., Parameswari, G. and Michael, A. 2009. Studies on antivenom activity of
Andrographis paniculata and Aristolochia indica plant extracts against Daboia russelli venom
by in vivo and in vitro methods. Indian J. Sci. Technol. 2(4): 76–79.
Meenatchisundaram, S., Priyagrace, S., Vijayaraghavan, R., Velmurugan, A., Parameswari, G. and
Michael, A. 2009. Antitoxin activity of Mimosa pudica root extracts against Naja naja and Bangarus
caerulus venoms. Bangladesh J. Pharmacol. 4(2): 105–109.
Melo, M.M., Habermehl, G.G., Oliveira, N.J.F., Nascimento, E.F., Santos, M.M.B. and Lúcia, M. 2005.
Treatment of Bothrops alternatus envenomation by Curcuma longa and Calendula officinalis
extracts and ar-turmerone. Arq. Bras. Med. Vet. Zootec. 57(1): 7–17.
Melo, M.M., Lúcia, M. and Habermehl, G.G. 2007. Plant extracts for topic therapy of Bothrops alternatus
envenomation. Braz. J. Pharmacogn. 17(1): 29–34.
Melo, P.A. and Ownby, C.L. 1999. Ability of wedelolactone, heparin, and para-bromophenacyl bromide
to antagonize the myotoxic effects of two crotaline venoms and their PLA2 myotoxins. Toxicon
37(1): 199–215.
Melo, P.A., do Nascimento, M.C., Mors, W.B. and Suarez-Kurts, G. 1994. Inhibition of the myotoxic
and hemorrhagic activities of crotalid venoms by Eclipta prostrata (Asteraceae) extracts and
constituents. Toxicon. 32(5): 595–603.
Mishal, H.B. 2002. Screening of anti-snake venom activity of Dichrostachys cinerea W.A.J. Nat.
Remedies 2(1): 92–95.
128 ETHNOBOTANY: Local Knowledge and Traditions
Mishal, R.H., Vadnere, G.P. and Mishal, H.B. 2014. Screening of anti snake venom potential of the
seed oil of Balanites aegyptiaca L. Del. J. Nat. Remedies 14(2): 126–131.
Molander, M., Nielsen, L., Sogaard, S., Staerk, D., Rosnted, N., Diallo, D., Chifundera, K.Z., van
Staden, J. and Jäger, A.K. 2014. Hyaluronidase, phospholipase A2 and protease inhibitory activity
of plants used in traditional treatment of snakebite-induced tissue necrosis in Mali, DR Congo
and South Africa. J. Ethnopharmacol. 18(157): 171–180.
Momoh, S., Friday, E.T., Raphael, E., Stephen, A. and Umar, S. 2012. Anti-venom activity of ethanolic
extract of Bridelia ferruginea leaves against Naja nigricollis venom. E3 J. Med. Res. 1(5): 69–73.
Mors, W.B., do Nascimento, M.C., Parente, J.P., da Silva, M.H., Melo, P.A. and Suarez-Kurtz, G.
1989. Neutralization of lethal and myotoxic activities of South American rattlesnake venom by
extracts and constituents of the plant Eclipta prostrata (Asteraceae). Toxicon. 27(9): 1003–1009.
Moura, V.M., Serra Bezerra, A.N., Mourão, R.H.V., Varjão Lameiras, J.L., Almeida Raposo, J.D., Sousa,
R.L., Boechat, A.L., Oliveira, R.B., Chalkidis, H.M. and Dos-Santos, M.C. 2014. A comparison
of the ability of Bellucia dichotoma Cogn. (Melastomataceae) extract to inhibit the local effects
of Bothrops atrox venom when pre-incubated and when used according to traditional methods.
Toxicon. 85: 59–68.
Moura, V.M., Silva, W.C.R., Raposo, J.D.A., Freitas-de-Sousa, L.A., Dos-Santos, M.C., Oliveira,
R.B. and Mourão, R.H.V. 2016. The inhibitory potential of the condensed-tannin-rich fraction
of Plathymenia reticulata Benth. (Fabaceae) against Bothropsatrox envenomation. http://dx.doi.
org/10.1016/j.jep.2016.02.047.
Mukherjee, A.K., Doley, R. and Saikia, D. 2008. Isolation of a snake venom phospholipase A2 (PLA2)
inhibitor (AIPLAI) from leaves of Azadirachta indica (Neem): mechanism of PLA2 inhibition
by AIPLAI in vitro condition. Toxicon. 51(8): 1548–1553.
Naik, B. and Sadananda. 2017. “Dry bite” in venomous snakes: a review. DOI: 10.1016/j.
toxicon.2017.04.015.
Nazato, V.S., Rubem-Mauro, L., Vieira, N.A., Rocha-Junior, D., dos, S., Silva, M.G., Lopes, P.S., Dal-
Belo, C.A., Cogo, J.C., dos Santos, M.G., da Cruz-Höfling, M.A. and Oshima-Franco, Y. 2010. In
vitro antiophidian properties of Dipteryx alata Vogel bark extracts. Molecules 15(9): 5956–5970.
Nishijima, C.M., Rodrigues, C.M., Silva, M.A., Lopes-Ferreira, M., Vilegas, W. and Hiruma-Lima, C.A.
2009. Anti-hemorrhagic activity of four Brazilian vegetable species against Bothrops jararaca
venom. Molecules 14(3): 1072–1080.
Núñez, V., Otero, R., Barona, J., Saldarriaga, M., Osorio, R.G., Fonnegra, R., Jiménez, S.L., Díaz,
A. and Quintana, J.C. 2004. Neutralization of the edema-forming, defibrinating and coagulant
effects of Bothrops asper venom by extracts of plants used by healers in Colombia. Braz. J. Med.
Biol. Res. 37(7): 969–977.
Ode, O.J. and Asuzu, I.U. 2006. The anti-snake venom activities of the methanolic extract of the bulb
of Crinum jagus (Amaryllidaceae). Toxicon. 48(3): 331–342.
Okonogi, T., Hattori, Z., Ogiso, A. and Mitsui, S. 1979. Detoxification by persimmon tannin of snake
venoms and bacterial toxins. Toxicon. 17: 324–327.
Oliveira, C.Z., Maiorano, V.A., Marcussi, S., Sant’ana, C.D., Januário, A.H., Lourenço, M.V., Sampaio,
S.V., França, S.C., Pereira, O.S. and Soares, A.M. 2005. Anticoagulant and antifibrinogenolytic
properties of the aqueous extract from Bauhinia forficata against snake venoms. J. Ethnopharmacol.
98(1-2): 213–216.
Omale, S., Aguiyi, J.C., Wannang, N.N., Ogbole, E., Amagon, K.I., Banwat, S.B. and Auta, A. 2012.
Effects of the ethanolic extract of Parinari curatellifolia on blood clotting factors in rats pretreated
with venom of Naja nigricolis. Drug Invention Today 4(4): 363–364.
Oshima-Franco, Y., Alves, C.M.V., Andréo Filho, N., Gerenutti, M., Cintra, A.C.O., Leite, G.B.,
Rodrigues-Simioni, L. and Silva, M.G. 2005. Neutralization of the neuromuscular activity of
bothropstoxin-I, a myotoxin from Bothrops jararacussu snake venom, by a hydroalcoholic extract
of Casearia sylvestris sw. (guaçatonga). J. Venom Anim. Toxins incl. Trop. Dis. 11(4): 465–478.
Oshima-Franco, Y., Rosa, L.J.R., Silva, G.A.A., Amaral Filho, J., Silva, M.G., Lopes, P.S., Cogo, J.C.,
Cintra, A.C.O. and Cruz-Höfling, M.A. 2012. Antibothropic action of Camellia sinensis extract
against the neuromuscular blockade by Bothrops jararacussu snake venom and its main toxin,
Bothropstoxin-I. Pharmacology, Dr. Luca Gallelli (ed.). ISBN: 978-953-51-0222-9, InTech,
Traditional Knowledge of Antivenom Plants 129
Shirwaikar, A., Rajendran, K., Bodla, R. and Kumar, C.D. 2004. Neutralization potential of Viper russelli
russelli (Russell’s viper) venom by ethanol leaf extract of Acalypha indica. J. Ethnopharmacol.
94(2-3): 267–273.
Sia, F.Y., Vejayan, J., Jamuna, A. and Ambu, S. 2011. Efficacy of tannins from Mimosa pudica and
tannic acid in neutralizing cobra (Naja kaouthia) venom. J. Venom. Anim. Toxins incl. Trop.
Dis. 27(1): 42–48.
Silva, J.F., Silva-Junior, A.A., Zucolotto, S.M. and Fernandes-Pedrosa, M. 2017. Medicinal plants for
the treatment of local tissue damage induced by snake venoms: An overview from traditional use
to pharmacological evidence. Evid Based Complementary Alt. Med. 2017, Article ID 5748256,
52 pages DOI: 10.1155/2017/5748256.
Silva, M.M., Seneviratne, S.S., Weerakoon, D.K. and Goonasekara, C.L. 2017. Characterization
of Daboia russelii and Naja naja venom neutralizing ability of an undocumented indigenous
medication in Sri Lanka. J. Ayurveda Integr. Med. 8(1): 20–26.
Soares, A.M., Ticli, F.K. and Marcussi, S. 2005. Medicinal plants with inhibitory properties against
snake venoms. Curr. Med. Chem. 12(22): 2625–2641.
Soares-Silva, J.O., Oliveira, J.L., Cogo, J.C., Tavares, R.V.S. and Oshima-Franco, Y. 2014.
Pharmacological evaluation of hexane fraction of Casearia gossypiosperma Briquet: Antivenom
potentiality. J. Life Sci. 8(4): 306–315.
Soni, P. and Bodakhe, S.H. 2014. Antivenom potential of ethanolic extract of Cordia macleodii bark
against Naja venom. Asian Pac. J. Trop. Biomed. 4 (Suppl 1): S449–S454.
Strauch, M.A., Tomaz, M.A., Monteiro-Machado, M., Ricardo, H.D., Cons, B.L., Fernandes, F.F., El-
Kik, C.Z., Azevedo, M.S. and Melo, P.A. 2013. Antiophidic activity of the extract of the Amazon
plant Humirianthera ampla and constituents. J. Ethnopharmacol. 145(1): 50–58.
Tan, N.H., Fung, S.Y., Sim, S.M. and Marinello, E. 2009. The protective effect of Mucuna pruriens
seeds against snake venom poisoning. J. Ethnopharmacol. 123: 356–358.
Tareen, R.B., Bibi, T., Khan, M.A., Ahmad, M. and Zafar, M. 2010. Indigenous knowledge of folk
medicine by the women of Kalat and Khuzdar regions of Balochistan, Pakistan. Pak J. Bot.
42(3): 1465–1485.
Tianyi, F.L., Dimala, C.A. and Feteh, V.F. 2017. Shortcomings in snake bite management in rural
Cameroon: a case report. BMC Res. Notes (2017) 10: 196. DOI: 10.1186/s13104-017-2518-8.
Ticli, F.K., Hage, L.I.S., Cambraia, R.S., Pereira, P.S., Magro, A.J., Fontes, M.R., Stábeli, R.G., Giglio,
J.R., França, S.C., Soares, A.M. and Sampaio, S.V. 2005. Rosmarinic acid, a new snake venom
phospholipase A2 inhibitor from Cordia verbenacea (Boraginaceae): antiserum action potentiation
and molecular interaction. Toxicon 46(3): 318–327.
Torres, M.C., Jorge, R.J., Ximenes, R.M., Alves, N.T.Q., Santos, J.V., Marinho, A.D., Monteiro,
H.S.A., Toyama, M.H., Braz-Filho, R., Silveira, E.R. and Pessoa, O.D. 2011. Solanidane and
iminosolanidane alkaloids from Solanum campaniforme. Phytochem. 97: 457–464.
Tribuiani, N., da Silva, A.M., Ferraz, M.C., Silva, M.G., Bentes, A.P., Graziano, T.S., dos Santos, M.G.,
Cogo, J.C., Varanda, E.A., Groppo, F.C., Cogo, K. and Oshima-Franco, Y. 2014. Vellozia flavicans
Mart. ex Schult. Hydroalcoholic extract inhibits the neuromuscular blockade induced by Bothrops
jararacussu venom. BMC Complement Altern. Med. 14: 48. DOI: 10.1186/1472-6882-14-48.
Tribuiani, N., Tavares, M.O., Santana, M.N., Fontana Oliveira, I.C., Amaral Filho, J.D., Silva,
M.G., Dos Santos, M.G., Cogo, J.C., Floriano, R.S., Cogo-Müller, K. and Oshima-Franco, Y.
2017. Neutralising ability of Terminalia fagifolia extract (Combretaceae) against the in vitro
neuromuscular effects of Bothrops jararacussu venom. Nat Prod. Res. 2: 1–5.
Ushanandini, S., Nagaraju, S., Harish Kumar, K., Vedavathi, M., Machiah, D.K., Kemparaju, K.,
Vishwanath, B.S., Gowda, T.V. and Girish, K.S. 2006. The anti-snake venom properties of
Tamarindus indica (Leguminosae) seed extract. Phytother. Res. 20(10): 851–858.
Ushanandini, S., Nagaraju, S., Nayaka, S.C., Kumar, K.H., Kemparaju, K. and Girish, K.S. 2009.
The anti-ophidian properties of Anacardium occidentale bark extract. Immunopharmacol.
Immunotoxicol. 31(4): 607–615.
Vale, F., Mendes, L.H., Fernandes, M.M., Costa, T.R., S. Hage-Melim, L.I., Sousa, A., Hamaguchi, M.,
Homsi- Brandeburgo, A., Franca, M.I., Silva, S.C., Pereira, P.S., Soares, A.M. and Rodrigues, V.M.
Traditional Knowledge of Antivenom Plants 131
2011. Protective effect of Schizolobium parahyba flavonoids against snake venoms and isolated
toxins. Curr. Top Med. Chem. 11(20): 2566–2577.
Veronese, E.L.G., Esmeraldino, L.E., Trombone, A.P.F., Santana, A.E., Bechara, G.H., Kettelhut,
I., Cintra, A.C.O., Giglio, J.R. and Sampaio, S.V. 2005. Inhibition of the myotoxic activity of
Bothrops jararacussu venom and its two major myotoxins, BthTX-I and BthTX-II, by the aqueous
extract of Tabernaemontana catharinensis A. DC. (Apocynaceae). Phytomed. 12(1-2): 123–130.
Wufem, B.M., Adamu, H.M., Cham, Y.A. and Kela, S.L. 2007. Preliminary studies on the anti-venim
potential and phytochemical analysis of the crude extracts of Balanites aegyptiaca (Linn.) Delile
on albino rats. Nat. Prod. Radiance 6(1): 18–21.
Xu, S., Zou, B., Yang, J., Yao, P. and Li, C. 2012. Characterization of a highly polymeric proanthocyanidin
fraction from persimmon pulp with strong Chinese cobra PLA2 inhibition effects. Fitoterapia
83(1): 153–160.
Yoshida, E.H., Ferraz, M.C., Tribuiani, N., Tavares, R.V.S., Cogo, J.C., dos Santos, M.G., Franco, L.M.,
Dal Belo, C.A., de Grandis, R.A., Resende, F.A., Varanda, E.A., Puebla, P., San Feliciano, A.,
Groppo, F.C. and Oshima-Franco, Y. 2015. Evaluation of the safety of three phenolic compounds
from Dipteryx alata Vogel with antiophidian potential. Chinese Medicine 6: 1–12.
CHAPTER 8
Introduction
The records of conscious use of plants other than food by human races have been
obliterated in remote historical past. When the “Vedas” appeared in written form,
the use of plants appeared to be the first documentary evidence as curative agent.
The subject ethnobotany gained importance at the beginning of 20th century. In
those days, it was thought that the knowledge of plants of different ethnic people
is the major source of ethnobotany. Those people had no written alphabet. It was
further conceived that discourses about the uses of plants by these aborigines and
ethnic people is ethnobotany. But the area of ethnobotany is deeper and wider.
Ethnobotany, as it stands now, is the domain of knowledge which researches
all sorts of plant uses including medicinal, cultural, primitive, agricultural or other
forms of anthropogenic uses.
Plants have been used as medicine from the beginning of civilization to present
day. Perhaps since Stone Age, plants are believed to have healing powers on man.
Ancient Vedas dating back between 3500 BC and 800 BC reveal many references
on medicinal plants. One of the remotest works in traditional herbal medicine is
1
Department of Sericulture, Raiganj University, Raiganj, Uttar Dinajpur, West Bengal-733134, India.
2
Plant Genetics and Molecular Breeding Laboratory, Department of Botany, University of North
Bengal, Raja Rammohunpur, Darjeeling, West Bengal-734013, India.
3
College para, Raiganj, Uttar Dinajpur, West Bengal-733134, India.
* Corresponding author: [email protected]
Ethnobotanical Study of Dakshin Dinajpur District of West Bengal—An Overview 133
“Virikshayurveda”, compiled even before the beginning of the Christian era. World’s
most ancient literary work, the “Rig Veda” was composed around 2000 BC (Bently
and Trimen 1980). About 200 years ago, Indian pharmacopoeia was dominated by
herbal medicines (Ernst 2005) and almost 25% of the drugs prescribed worldwide
were obtained from plants. Of the 252 drugs considered as basic and essential by
the WHO, 11% are exclusively of plant origin and a significant number are synthetic
drugs obtained from natural precursors (Rates 2001).
Dakshin Dinajpur, consisting of eight developmental blocks, is primarily an
agriculturally sustained district. The principal tribal communities are—Santal,
Munda, Oraon, along with Scheduled Caste communities like Rajbanshis. This
district has an old folk culture of using herbal medicines. However, the importance
and such use of medicinal plants/plant parts are being lost due to rapid urbanization
and deforestation. As a result, many useful medicinal plants are becoming threatened
and precious knowledge is lost. An attempt has been made to accumulate the
previous ethnobotanical data in a nutshell so that the knowledge of various ethnic
people never get lost and the knowledge be used in different pharmaceutical industry
to exploit the active principal constituted of different plants. It may give a scientific
base on the ethnobotanical study.
Fig. 8.2. Traditional healers and their medicinal preparations of Dashin Dinajpur district.
Ethnobotanical Study of Dakshin Dinajpur District of West Bengal—An Overview 137
‘Budhasari’, etc. Besides ‘Khan’, some of the other important folk culture of the
district are Natua, Jang Gan, Mokha dance (Mask Dance), Halua-Haluani, Bislihava,
Saitpir (Satyapir Gan), Jalmanga Gan, Khaja Gan, Chorchunni, etc. In addition
to folk culture, the district has some historical and tourist sports like Dhaldighi,
Dumduma, Bangarh, Mahipaldighi, Bairhatta and Kichaka Kunda, Tapan Dighi,
District Library, College Museum, Pancha Ratna Temple, etc.
Scientific Name and Voucher Vernacular Name Family Parts used Medicinal uses and preparation
Specimen Number
Abroma augusta (L.) L.f. DD-12 Ulatkambol Sterculiaceae Petiole Young petiole cut into small pieces and kept in a glass of
water for overnight and infusion is used early morning on
an empty stomach to cure “meho” (a sexual disease) and
physical weakness.
Abrus precatorius L. DD-10 Kanch Papilionaceae Root Roots are used for “Meho” (a sexual disease), jaundice and
also used as abortifacient.
Acacia nilotica (L.) Delile * DD-130 Babla Mimosaceae Stem bark Stem bark decoction used to treat cough, diarrhoea,
dysentery, indigestion, acidity, “Meho” (a sexual disease)
and diabetes.
Achyranthes aspera L. DD-78 Apang/Chatchota Amaranthaceae Root Stem and root (2–3 piece) decoction mixed with “Ada”
(Zingiber officinale) and used in jaundice.
Acmella oleracea (L.) R.K.Jansen* Rasun sag Asteraceae Whole plant Whole plant eaten as vegetables to treat body pain,
DD-25 especially after child birth.
Acorus calamus L. DD-23 Bach Acoraceae Rhizome Fresh rhizome juice clears the vocal cord.
138 ETHNOBOTANY: Local Knowledge and Traditions
Aegle marmelos (L.) Corr. DD-58 Bel Rutaceae Fruit One teaspoonful of young dried fruits powder mixed with
water is given early morning on an empty stomach to cure
dysentery and gastric problems.
Alocasia macrorrhizos (L.) G.Don* Man-kachu Araceae Peliole Petiole ash mixed with coconut oil and applied as
DD-39 emollient on carbuncle.
Alstonia scholaris (L.) R. Br.* DD-27 Chatim/Chatan Apocyanaceae Stem bark Stem bark paste applied on breast for better lactation.
Amaranthus spinosus L. DD-16 KantaKhuria Amaranthaceae Root Mature root decoction gives physical strength and used in
indigestion problem, dysentery and diphtheria.
Ampelocissus latifolia (Roxb.) Planch.* Goalilata Vitaceae Root Root paste mixed with 12 “Golmarich” (Piper nigrum) and
DD-11 applied to cure gout and rheumatism.
Andrographis paniculata (Burm. f.) Kalmegh Acanthaceae Leaf Leaf juice used for cold and cough, diabetes and leaf
Wall. Ex Nees DD-24 paste applied on hair before 30 minutes of bath to control
dandruff.
Argemone mexicana L.* DD-01 Siyalkanta Papaveraceae Root Root juice used for piles.
Aristolochia indica L.* DD-26 Iswarmul Aristolochiaceae Root Root and leaf juice is given early morning to cure
stomachache, fever, indigestion problem and diarrhoea.
Artemisia vulgeris L. DD-35 Nagdona Asteraceae Leaf Leaf paste applied externally on the forehead to reduce
headache and sinus problem.
Averrhoa carambola L.* DD-33 Kamranga Oxalidaceae Fruit roasted fruit juice mixed with a pinch of sugar is given
early morning to cure cough and bronchitis.
Azadirachta indica A. Juss. DD-103 Neem Meliaceae Stem bark Stem bark and leaves boiled with water and applied on
carbuncle, boil and skin diseases for quick healing.
Baccharoides anthelmintica (L.) Somraji Asteraceae Seed Seeds are crushed with cream of milk and applied to cure
Moench.* DD-61 carbuncle.
Bambusa tulda L.* DD-21 Bansh Poaceae Stem Juice of roasted young shoot is applied to cure earache.
Basella alba L.* DD-77 Pui Basellaceae Stem Dried stem ash used as tooth paste to cure pyorrhoea.
Bauhinia acuminata L.* DD-59 SwetKancan Caesalpiniaceae Flower Dried flowers crushed and then lightly wormed with
mustered oil are applied externally to cure skin diseases.
Blumea lacera (Burm. f.) DC. DD-22 Kukurmuta Asteraceae Root Root (2–3 pieces) decoction mixed with “Ada” (Zingiber
officinale) is given to cure flatulence and indigestion
problem.
Boerhavia diffusa L. DD-74 Punarnaba Nyctaginaceae Whole plant Whole plant juice is given to cure burning sensation during
urination.
Bombax ceiba L. DD-66 Shimul Bombacaceae Root Fresh root (1–2 years old plant) used in “Meho” (a sexual
disease) and physical weakness.
Ethnobotanical Study of Dakshin Dinajpur District of West Bengal—An Overview
Scientific Name and Voucher Vernacular Name Family Parts used Medicinal uses and preparation
Specimen Number
Borassus flabellifer L.* DD-72 Tal Palmae Root Root mixed with Churchuri roots (Achyranthes aspera) are
boiled and used for gargling to cure toothache.
Bryophyllum pinnatum (Lam.) Oken Patharkuchi Crassulaceae Leaf Fresh leaf juice is used for dissolving kidney stones and
DD-41 used to treat cold and cough, flatulence and acidity. Leaf
paste applied also on burns for quick healing from burning
sensation.
Butea monosperma (Lam.) Taub. Palash Papilionaceae Leaf Leaf juice used as aphrodisiac and enhances sperm count.
DD-20
Cajanus cajan (L.) Millsp. DD-68 Arhar Papilionaceae Leaf Fresh leaf juice is given early morning to treat jaundice.
Calotropis gigantea (L.) Dryand. Akanda Asclepiadaceae Leaf A leaf warm with “Ghee” is applied to get relief from
DD-105 paralysis, rheumatism and body pain.
Canna indica L.* DD-54 Kalabati Cannaceae Root Root paste applied on the upper surface of the cheek to
reduce toothache.
Cassia fistula L. DD-87 Bandarlathi Caesalpiniaceae Leaf Tender leaf juice is given to cure constipation.
Centella asiatica (L.) Urban DD-32 Thankuni/ Umbelliferae Leaf Fresh leaves (5–6) chewed early morning preferably on
140 ETHNOBOTANY: Local Knowledge and Traditions
Scientific Name and Voucher Vernacular Name Family Parts used Medicinal uses and preparation
Specimen Number
Curcuma aromatica Salisb.* DD-43 Shut Zingiberaceae Rhizome Fresh rhizome juice mixed with honey is given to children
to cure cough and bronchitis.
Cuscuta reflexa Roxb DD-84 Swarnalata Convolvulaceae Whole plant Whole plant decoction is to be taken on an empty stomach
to cure gonorrhoea.
Cyanthillium cinereum (L.) H.Rob.* Sahadebi Asteraceae Root Fresh root juice used in piles, diarrhoea and stomachic.
DD-02
Cynodon dactylon (L.) Pers. DD-31 Durba Poaceae Whole plant Whole plant chewed and applied on cuts and wounds for
stopping bleeding. Fresh plant decoction mixed with one
slice of Curcuma longa is given to cure leucorrhoea and
infertility.
Cyperus rotundus L. DD-56 MuthaGhas Cyperaceae Tuber Juice of tuber with a pinch of table salt is given in morning
on an empty stomach to cure chronic dysentery. Paste of
the whole plant mixed with “Ada” (Zingiber officinale) is
applied to cure boils on finger tips (Thosa).
Datura metel L. DD-127 Dhutura Solanaceae Leaf Leaf paste applied as massage balm to get relief from
142 ETHNOBOTANY: Local Knowledge and Traditions
rheumatic pain.
Deeringia amaranthoides (Lam.) Atmora/Atmutha Amaranthaceae Stem Young mature stem combining with “Apang”
Merr.* DD-79 (Achyranthes aspera) stem made into a chain and used to
cure jaundice. Leaf also eaten as vegetable.
Desmodium triflorum (L.) DC. DD-122 Tin pata/Tepati Papilionaceae Leaf Fresh leaves’ juice is given on an empty stomach to cure
flatulence.
Dioscorea alata L.* DD-42 Poraalu/Mach alu Dioscoreaceae Rhizome Rhizome eaten as vegetable.
Dregea volubilis (L.f.) Benth. ex Jukti Asclepiadaceae Stem Stem mixed with “Golmarich” (Piper nigram) and made
Hook.f.* DD-52 into paste and externally applied for bone fracture.
Drynaria quercifolia (L.) J. Smith* Pokhiraj Polypodiaceae Leaf Dry leaf powder mixed with 12–18 “Golmarich” (Piper
DD-90 nigrum) and warmed in mustard oil and is applied locally
to reduce muscular pain.
Eclipta prostrata (L.) L. DD-08 Kesut Asteraceae Whole plant Whole plant juice is given to get relief from irritation and
inflammation during urination. The whole plant paste is
also applied on hair before 30 minutes of bath to reduce
hair fall and promote hair growth.
Eleusine indica (L.) Gaertn DD-120 KanChulkani Poaceae Root Fresh root decoction mixed with sugar is given in morning
on an empty stomach to cure “Meho” (a sexual disease).
Euphorbia hirta L. DD-48 Dudhkushi Euphorbiaceae Whole plant Whole plant paste used to treat rheumatism.
Euphorbia nerifolia L.* DD-88 ManasaSij Euphorbiaceae Leaf Fresh leaves are crushed and fried in mustard oil and
gently applied on the chest to cure bronchitis.
Flacourtia indica (Burm. f.) Merr. Bainchi/Paniala Flacourtiaceae Stem bark Stem bark mixed with stem bark of “Shimul” (Bombax
DD-45 ceiba) and boiled in water is given twice a day to cure
physical weakness, Leucorrhoea and “Meho” (a sexual
disease).
Geodorum densiflorum (Lam.) Schlt.* Bon-ada Orchidaceae Tuber Tuber paste applied on joint pain and arthritis.
DD-70
Gloriosa superba L.* DD-09 Ulatchandal Liliaceae Root Tuber paste mixed with “Ada” (Zingiber officinale) and
“Tepati” (Desmodium triflorum) applied to cure joint pain.
Glycosmis pentaphylla (Retz.) DC. Atiswar Rutaceae Root Root paste applied for rupturing the boil or carbuncle and
DD-110 getting relief from joint pain. Mature stem used as tooth
brush.
Heliotropium indicum L. DD-55 Hatisur Boraginaceae Root Root paste warm with mustard oil and applied to cure
rheumatism.
Helminthostachys zeylanica (L.) Hook.* Akbir Ophioglossaceae Rhizome Rhizome paste applied to cure arthritis.
Ethnobotanical Study of Dakshin Dinajpur District of West Bengal—An Overview
DD-115
Scientific Name and Voucher Vernacular Name Family Parts used Medicinal uses and preparation
Specimen Number
Hemidesmus indicus (L.) R. Br. ex Anantamul Asclepiadaceae Root Root juice is given to promote sexual debilities and
Schult.* DD-73 physical weakness.
Hibiscus rosa-sinensis L. DD-71 Jaba Malvaceae Leaf Leaves’ (5–7) juice mixed with “Gur” (Jaggery) taken on
an empty stomach to reduce dysentery.
Holarrhena pubescens Wall. ex G. Don Kurci/Indrajab Apocyanaceae Stem bark Stem bark infusion is given early morning to cure chronic
DD-86 dysentery and seed powder mixed with water is used in
diabetes and guinea worm.
Hygrophila auriculata (Schumach.) Kulekhara Acanthaceae Leaf Fresh leaves’ (5–7) juice is taken twice daily to get relief
Heine DD-114 from allergy.
Ipomoea mauritiana Jacq.* DD-67 BhuiKumra Convolvulaceae Tuber One teaspoonful tuber powder mixed with lukewarm milk
is given during bed time as sexual stimulant.
Jatropha curcus L.* DD-29 Varenda Euphorbiaceae Latex Latex used in toothache.
Jatropha gossypiifolia L. DD-47 LalVarenda Euphorbiaceae Latex Latex used in pyorrhoea and applied on boil.
Justicia adhatoda L. DD-36 Harbashak Acanthaceae Leaf Leaves boiled with water and sugar candy, mixture is
given for better lactation.
144 ETHNOBOTANY: Local Knowledge and Traditions
Justicia gendarussa Burm. f.* DD-76 Bishtarak Acanthaceae Whole plant Whole plant paste used in rheumatism.
Lawsonia inermis L.* DD-91 Mehendi Lythraceae Root Root juice is used as sexual stimulant.
Leucas aspera (Willd.) Link.* DD-97 Dandakalash/Dulfi Lamiaceae Root Root juice given on an empty stomach and the smell of the
plant allowed to inhale for treatment of Tuberculosis.
Litsea glutinosa (Lour.) C. B. Rob. Pipulti/Darodmaida Lauraceae Leaf Leaf juice mixed with a pinch of salt and turmeric powder
DD-104 is given to cure dysentery and spermatorrhoea.
Ludwigia adscendens (L.) H. Hara Keshra-dam Onagraceae Whole plant Whole plant paste applied for bone fracture and
DD-93 rheumatism.
Madhuca longifolia (Koen. ex L.) Mahua Sapotaceae Stem bark Stem bark boiled with water and the extract is used to cure
Macbride DD-53 physical weakness.
Mangifera indica L. DD-14 Aam Anacardiaceae Leaf Bark decoction mixed with lime water is given to cure
dysentery and diarrhoea. Tender leaf juice used for
stomachic.
Marsilea quadrifolia L. DD-06 Susni Marsileaceae Leaf Leaf juice mixed with a cup of lukewarm milk given at
bed time to cure insomnia.
Meyna spinosa Roxb. ex Link.* DD-18 Moyenakanta Rubiaceae Spine Spine fried with mustard oil is applied to cure piles.
Mimosa pudica L. DD-94 Lajjabati Mimosaceae Root Fresh root boiled with water is used as gargle to cure
toothache. Root decoction also used for leucorrhoea and
blood dysentery.
Molineria capitulata (Lour.) Herb.* Bansmora Liliaceae Root Root juice is given early morning to cure piles.
DD-17
Momordica charantia L. DD-19 Karola Cucurbitaceae Leaf Leaf decoction and fruit juice is used to treat diabetes,
allergy and guinea worms.
Momordica dioica Roxb. ex Willd. Bhat-kalla Cucurbitaceae Fruit Fruit eaten as vegetable to control blood sugar level.
DD-109
Mucuna pruriens (L.) DC.* DD-15 Alkusi Papilionaceae Seed The seeds are fried with “Ghee” and sugar and pills are
made. Each pill taken during bed time as stimulant and for
vitality.
Murraya koenigii (L.) Spreng. DD-28 Curry Pata Rutaceae Leaf Leaf juice is given early morning to control blood sugar.
Nyctanthes arbor-tristis L. DD-30 Shiuly/Sephali Oleaceae Stem bark Stem bark and leaf juice is given to control remittent fever
and blood sugar.
Nymphaea rubra Roxb. ex Andrews* Lalsaluk Nymphaeaceae Flower Dried flowers’ powder mixed with water is given to cure
DD-13 piles. Dried flowers mixed with root of Eleusine indica
and a pinch of sugar is given on an empty stomach to cure
Ethnobotanical Study of Dakshin Dinajpur District of West Bengal—An Overview
leucorrhoea.
Scientific Name and Voucher Vernacular Name Family Parts used Medicinal uses and preparation
Specimen Number
Oxalis corniculata L. DD-92 Amrul Oxalidaceae Leaf Leaf decoction used to cure smokers cough.
Ocimum americanum L. NBU-09797 Bon tulsi Lamiaceae Leaf/Seed 1. Infusion and mucilaginous seeds are given on an empty
stomach to cure flatulence.
2. Half teaspoon of seed dust mixed with one cup of
lukewarm milk is given continuously for 7 days during
bed time to increase sexual potentiality.
3. The leaf used as mole repellents.
4. Dried burnt leaf smoke used for mosquito repellent.
Ocimum × africanum Lour.* NBU- Lebu/bon tulsi Lamiaceae Leaf/Seed 1. Fresh leaves are made into paste and applied
09798 consecutively for 7 days before 30 minutes of bath to
cure skin diseases.
2. 10–15 seeds mixed with drop of water and the
mucilaginous seeds are applied on boils for quick
rupture.
3. Leaf paste used on poisonous insect bites.
Ocimum basilicum L. NBU-09799 Babu/babuitulsi Lamiaceae Leaf 1. Fresh leaves’ paste is applied on the forehead to get
146 ETHNOBOTANY: Local Knowledge and Traditions
Phyla nodiflora (L.) Greene DD-98 Koi Okhra Verbenaceae Whole plant Whole plant paste used in bone fracture.
147
Scientific Name and Voucher Vernacular Name Family Parts used Medicinal uses and preparation
Specimen Number
Phyllanthus emblica L. DD-03 Amlaki Phyllanthaceae Fruit Infusion of fruit is useful in acidity, constipation, insomnia
and also in diabetes.
Physalis peruviana L.* DD-116 Fatki Solanaceae Root Fresh root juice mixed with a few drops of honey is given
to cure whooping cough.
Piper betel L.* DD-111 Pan Piperaceae Leaf Leaf juice is given to cure indigestion and killing lice.
Piper longum L. DD-44 Pipul Piperaceae Whole plant Whole plant cooked as vegetable is given after child birth
for better lactation and relief from birth pain.
Plumbago zeylanica L. DD-113 Sadachita Plumbaginaceae Root The root paste is used as emollient for gout.
Pongamia pinnata (L.) Pierre* DD-04 Karanja/Gokaranja Papilionaceae Seed Seed oil is useful for hair growth and gout. Stem helpful in
reducing toothache when used as tooth brush.
Portulaca oleracea L.* DD-75 Nunia sag Portulacaceae Whole plant Whole plant cooked as vegetable to reduce constipation.
Premna serratifolia L.* DD-07 Ganiari Verbenaceae Leaf Dry leaf infusion is given on an empty stomach to cure
indigestion problem.
Psidium guajava L.* DD-100 Peyara Myrtaceae Leaf Tender leaves (2–3) chewed to cure mouth ulcer,
148 ETHNOBOTANY: Local Knowledge and Traditions
problems.
Table 8.1 contd. …
149
…Table 8.1 contd.
Scientific name and voucher specimen Vernacular name Family Parts used Medicinal uses and preparation
number
Terminalia bellirica (Gaertn.) Roxb. Bahera Combretaceae Fruit Infusion of fruit is given in morning on an empty stomach
DD-119 to cure chronic dysentery, piles and constipation.
Terminalia chebula Retz. DD-121 Haritaki Combretaceae Fruit Fruit infusion is given early morning on an empty stomach
to promote liver functions and digestion.
Thunbergia laurifolia Lindl.* DD-60 SwetMahakal Acanthaceae Leaf Leaf mixed with “Durba” (Cynodon dactylon) is given to
cure leucorrhoea.
Tinospora sinensis (Lour.) Merr. DD-47 Gulancha Menispermaceae Stem Stem (1.5 kg) boiled with water (3 lit) and made into 1 lit;
from there half cup of mixture is given daily on an empty
stomach to control blood sugar, cholesterol and physical
weakness.
Trichosanthes dioica Roxb.* DD-96 Patol Cucurbitaceae Root Fresh root juice is given early morning on an empty
stomach to expel the intestinal worm of children.
Tylophora indica (Burm.f.) Merr.* Antamul Asclepiadaceae Leaf Leaf decoction is given to cure “Meho” (a sexual disease).
DD-69
150 ETHNOBOTANY: Local Knowledge and Traditions
Vanda tessellata (Roxb.) G. Don DD-63 Rasna/Pargacha Orchidaceae Root Root juice is given to cure physical weakness and promote
sexual performances.
Vitex negundo L. DD-25 Nishinda Verbenaceae Leaf Dry leaves boiled with mustard oil are applied to cure
rheumatism. Leaf decoction used also in fever and
diabetes.
Zingiber montanum (J. Koenig) Link ex Bon Ada/Taraj Zingiberaceae Rhizome Infusion of the fresh rhizome is given to cure leucorrhoea
A. Dietr.* DD-34 and physical weakness.
Zingiber zerumbet (L.) Roscoe ex Sm.* Jabakusum Zingiberaceae Rhizome Fresh rhizome juice mixed with “Aswagandha” (Withania
DD-62 somnifera) is given to cure leucorrhoea and physical
weakness.
* New records/claims.
Ethnobotanical Study of Dakshin Dinajpur District of West Bengal—An Overview 151
Dakshin Dinajpur. The study revealed that 39 plants were used as herbal medicine
by different ethnic communities, namely Santhals and Mundas residing along the
basin of the River Atreyee. Santhals are the dominant tribe in the study area, using
the maximum number (67) of plants as indigenous health care system, and it was
followed by Munda tribe (29). Further, they identified 62 plant species belonging
to 34 families used by Santal, Oraon, Munda and other communities (Polia, Sabar,
Lodha) for medicinal purposes in Hili Block of Dakshin Dinajpur district, West
Bengal (Talukdar and Talukdar 2013). The study revealed that leaves of the plant
species are frequently used by ethnic people for medicinal purposes. Among
the tribals, Santals are the best in acquiring, maintaining and using traditional
knowledge of herbal plants. Recently, Chowdhury et al. (2014a) documented some
traditional uses of plants by the different communities of Dakshin Dinajpur district.
Results revealed that the maximum number of plants was used in gastrointestinal
problems followed by gynaecological problems. The study showed that among the
various plant parts used, leaf was mostly used for medicinal preparation followed by
root, whole plant, stem bark, etc. Total 132 plant species belonging to 65 families
under 120 genera were recorded in the aforementioned study. Though all the 132
plants have their medicinal values, but these were unveiled before the study, and
most importantly 56 plants are found to have medicinal importance, which was
not known before the study (Table 8.1).
North Bengal plains (Terai region of Darjeeling district, the districts of Jalpaiguri,
Koch bihar, Uttar Dianjpur, Dakshin Dinajpur, and Malda) of West Bengal, India.
Conclusion
The value of medicinal plants, herbs and spices as herbal remedies is getting lost
due to lack of awareness, urbanization, deforestation and modernization. On the
other hand, some traditional practitioners had a false apprehension that propagating
the knowledge of medicinal plants by common people may reduce their efficacy
and thus they kept it a secret. However, newer generations are not very keen to
retain this tradition based knowledge from their predecessors. As a result, important
knowledge based tradition is fading away. Therefore, in the present chapter, efforts
have been made to accumulate traditional knowledge of the different tribal and
non-tribal communities of Dakshin Dinajpur district before this huge wealth of
traditional knowledge is lost forever and hence it must be documented properly. In
conclusion, on the basis of the ethnobotanical review of Dakshin Dinajpur district,
further phytochemical investigation is needed for clinical trials to test their efficacy
and to develop a new herbal drug. Hopefully this documentation will serve for the
future generations, researchers and common people as a whole.
References
Agarwal, S., Kumar, V.R. and Kumar, A. 2013. Ethnobotanical studies on Ocimum spp. in Rajasthan,
India. Int. Res. J. Pharm. 4(4): 228–231.
Banerjee, R.N. and Ghora, C. 1996. On the domestic use of some unreported plants of West Dinajpur
district (WB). J. Econ. Tax. Bot. Addl. Ser. 12: 325–328.
Bently, R. and Trimen, H. 1980. Medicinal Plants. I-IV, J & A. Publishers, Churchill, London.
Chaudhuri Rai, H.N. and Pal, D.C. 1976. Preliminary observation on ethnobotany of Medinipur district,
West Bengal, India. Ind. Mus. Bull. 11(2): 51–53.
Chopra, R.N. 1953.Glossary of Indian medicinal plants, CSIR, New Delhi.
Chopra, R.N., Nayar, S.I. and Chopra, I.C. 1956. Glossary of Indian Medicinal Plants. CSIR, New Delhi.
Chowdhury, T., De Sarker, D. and Saha, M. 2011. Survey of plants used for the treatment of diabetes
in Dinajpur (Uttar & Dakshin) and Malda districts of Paschimbanga. pp. 295–299. In: Ghosh, C.
and Das, A.P. (eds.). Proceeding, Recent Studies in Biodiversity and Traditional Knowledge in
India. Gour Mahavidyalaya, Malda.
Chowdhury, T., De Sarker, D. and Roy, S.C. 2014a. Local folk use of plants in Dakshin Dinajpur district
of West Bengal, India. Int. Res. J. Biological. Sci. 3(5): 67–79.
Chowdhury, T., Roy, S.C. and De Sarker, D. 2014b. Wild edible plants of Uttar Dinajpur district, West
Bengal. Life Sci. Leaflets 47: 20–36.
Chowdhury, T., Mandal, A., Jana, A.K., Roy, S.C. and De Sarker, D. 2016. Study of phytosociology
and ecology of naturally growing Ocimum species with their conservational strategies in Dakshin
Dinajpur district of West Bengal. Acta Ecol. Sin. 36: 483–491.
Chowdhury, T. 2017. Ethnobotany of Dakshin Dinajpur district with special reference to diversity and
conservation of Ocimum species. Ph. D. Thesis Univ. of North Bengal.
Chowdhury, T., Mandal, A., Roy, S.C. and De Sarker, D. 2017. Diversity of the genus Ocimum
(Lamiaceae) through morpho-molecular (RAPD) and chemical (GC-MS) analysis. J. Genet. Eng.
Biotechnol. 15: 275–286.
Cohen, M.M. 2014. Tulsi—Ocimum sanctum: A herb for all reasons. J. Ayurveda. Integr. Med. 5(4):
251–259.
CSIR. 1966. The Wealth of India. A dictionary of Indian raw materials and industrial products. Vol. VII:
N-Pe. Publications and Information Directorate, CSIR, New Delhi, India, pp. 79–89.
Das, S.K. and Vasudevan, D.M. 2006.Tulsi: The Indian holy power plant. Nat. Prod. Rad. 5(4): 279–83.
Ethnobotanical Study of Dakshin Dinajpur District of West Bengal—An Overview 155
De, J.N. 1965. Some minor plant-fibres of aboriginal usage in the district of Purulia (West Bengal).
Bull. Bot. Soc. Bengal. 19(2): 67–72.
De, J.N. 1969. Further observation on the ethnobotany of Purulia District in West Bengal. Indian
Forester. 95(8): 551–559.
De Sarker, D., Chowdhury, T. and Saha, M. 2011. Biodiversity and medicinal plants of West Dinajpur
and Malda, Vol. 1, Raiganj College (University College), Raiganj, Uttar Dinajpur, West Bengal.
Ernst, E. 2005. The efficacy of herbal medicine—an overview. Fund. Clin. Pharmacol. 19(4): 405–409.
Galav, P., Jain, A. and Katewa, S.S. 2013. Traditional veterinary medicines used by livestock owners
of Rajasthan, India. Indian J. Tradit. Know. 12(1): 47–55.
Ghosh, A. 1986. A preliminary report on the ethnobotanical survey of Cooch Behar district, West Bengal.
J. Bengal. Nat. Hist. Soc. 5(1): 69–73.
Ghosh, G.R. 1995. Tulasi (N.O. Labiatae, Genus-Ocimum). New Approaches to Medicine and Health
(NAMAH) 3: 23–29.
Jain, S.K. and De, J.N. 1964. Some less known plants foods among the tribals of Purulia, West Bengal.
Sci. Cult. 30: 285–286.
Jain, S.K. and Tarafder, C.R. 1970. Medicinal plant-lore of Santal (A revival of P. O. Boddings work).
Econ. Bot. 24: 241–278.
Joshi, A.R. and Joshi, K. 2000. Indigenous knowledge and uses of medicinal plants by local communities
of the Kali Gandaki Watershed area, Nepal. J. Ethnopharmacol. 73(12): 175–183.
Kamboj, V.P. 2000. Herbal medicine. Current. Sci. 78(1): 35–39.
Kashyap, C.P., Kaur, R., Vikrant, A. and Kumar, V. 2011. Therapeutic potency of Ocimum
Kilimandscharicum Guerke—A review. Global J. Pharmacol. 5(3): 191–200.
Kirtikar, K.R. and Basu, B.D. 1975. Indian Medicinal Plants. Vol. 3 (2nd Eds.). Bishen Singh Mahendra
Pal Singh, New Connaught Place, Dehradun, India, pp. 1965–1968.
Kumar, A., Tiwari, D.D. and Tiwari, J.P. 2006. Ethnomedicinal knowledge among Tharu tribe of
Devipatan Division, UP, India. Indian J. Tradit Know. 5(3): 310–313.
Kundu, S. and Bag, A. 2012. Indigenous health care practices among Rajbanshi of Dakshin Dinajpur,
West Bengal. Ethno. Med. 6(2): 117–120.
Mamun-Or-Rashid, A.N.M., Azam, M.M., Dash, B.K., Hafiz, F.B. and Sen, M.K. 2013.
Ethnomedicobotanical study on Ocimum sanctum L. (Tulsi)—a review. Mintage. J. Pharm. Med.
Sci. 2(2): 37–42.
Mitra, S. and Mukherjee, S.K. 2005a. Ethnobotanical usages of grasses by the tribals of West Dinajpur
district, West Bengal. Indian J. Tradit. Know. 4(4): 396–402.
Mitra, S. and Mukherjee, S.K. 2005b. Root and rhizome drugs used by the tribals of West Dinajpur in
Bengal. J. Trop. Med. Plants 6(2): 301–315.
Mitra, S. and Mukherjee, S.K. 2007. Plants used as ethnoveterinary medicine in Uttar and Dakshin
Dinajpur districts of West Bengal, India. pp. 117–122. In: Das, A.P. and Pandey, A.K. (eds.).
Advances in Ethnobotany. Bishen Singh Mahendra Pal Singh, Dehra Dun, India.
Mitra, S. and Mukherjee, S.K. 2009. Some abortifacient plants used by the tribal people of West Bengal.
Nat. Prod. Rad. 8(2): 167–171.
Mitra, S. and Mukherjee, S.K. 2010. Ethnomedicinal uses of some wild plants of North Bengal plain
for gastro-intestinal problems. Indian J. Tradit. Know. 9(4): 705–712.
Mitra, S. and Mukherjee, S.K. 2011. Plants used for the treatment of diabetes in West Bengal, India. J.
Trop. Med. Plants 12(1): 99–105.
Mitra, S. and Mukherjee, S.K. 2013. Flora and ethnobotany of West Dinajpur district, West Bengal.
Bishen Singh Mahendra Pal Singh, Dehra Dun.
Molla, H.A. and Roy, B. 1984. Folklore about some medicinal plants from the tribal areas of Jalpaiguri
district, West Bengal. Bull. Bot. Surv. India 26(3-4): 160–163.
Molla, H.A. and Roy. B. 1985. Traditional uses of some medicinal plants by the Rabha tribals in
Jalpaiguri district, West Bengal. J. Econ. Taxon. Bot. 7(3): 578–580.
Molla, H.A. and Roy, B. 1996. Some ethnobotanical claims from the Jalpaiguri district of West Bengal.
J. Econ. Tax. Bot. Addl. Ser. 12: 322–324.
Nadkararni, A.K. and Nadkarni, K.M. 1976. Indian Materia Medica. Popular Prakashan Pvt. Ltd.,
Bombay.
156 ETHNOBOTANY: Local Knowledge and Traditions
Naghibi, F., Mosaddegh, M., Motamed, S.M. and Ghorbani, A. 2005. Labiatae family in folk medicine
in Iran: from ethnobotany to pharmacology. Iran. J. Pharm. Res. 4(2): 63–79.
Pagan, J.A. and Pauly, M.V. 2005. Access to conventional medical care and the use of complementary
and alternative medicine. Health Affairs 24(1): 225–262.
Pal, D.C. and Jain, S.K. 1989. Notes on Lodha medicine in Medinipur district, West Bengal, India.
Econ. Bot. 43(4): 464–470.
Pant, N.C., Pandey, D.K., Banerjee, S.K. and Mishra, T.K. 1993. Some common ethnobotanical
practices of Lodha community of Midnapore, West Bengal. J. Trop. Forestry 9(3): 215–218.
Prabhu, K.S., Lobo, R., Shirwaikar, A.A. and Shirwaikar, A. 2009. Ocimumgratissimum: a review of its
chemical, pharmacological and ethnomedicinal properties. Open Complement Med. J. 1(1): 1–15.
Prajapati, N.D., Purohit, S.S., Sharma, A.K. and Kumar, T. 2003. A hand book of medicinal plant.
Agrobios, India, pp. 367.
Ragupathy, S., Steven, N.G., Maruthakkutti, M., Velusamy, B. and Ul-Huda, M.M. 2008. Consensus of
the ‘Malasars’ traditional aboriginal knowledge of medicinal plants in the Velliangiri holy hills,
India. J. Ethnobiol. Ethnomed. 4(8): 1–14.
Rates, S.M.K. 2001. Plants as source of drugs. Toxicon 39(5): 603–613.
Saha, M.R. and De Sarker, D. 2013. Medicinal properties of ethnobotanically important plants of
Malda and Uttar Dinajpur districts: a review. pp. 209–226. In: Sen, A. (ed.). Biology of Useful
Plants and Microbes.
Saha, M.R., De Sarker, D., Kar, P., Sen Gupta, P. and Sen, A. 2014a. Indigenous knowledge of plants
in local healthcare management practices by tribal people of Malda district, India. J. Intercult.
Ethnopharmacol. 3(4): 179–185.
Saha, M.R., De Sarker, D. and Sen, A. 2014b. Ethnoveterinary practices among the tribal community
of Malda district of West Bengal, India. Indian J. Tradit. Know. 13(2): 359–367.
Saha, M.R., Rai, R., Kar, P., Sen, A. and De Sarker, D. 2015. Ethnobotany, traditional knowledge and
socioeconomic importance of native drink among the Oraon tribe of Malda district in India.
J. Intercult. Ethnopharmacol. 4(1): 34–39.
Saha, M.R., Dey, P., Sarkar, I., Kar, P., De Sarker, D., Das, S., Haldar, B., Chaudhuri, T.K. and Sen,
A. 2017. Acacia nilotica (L.) Delile could be a potential drug combating diabetes: an evidence
based and in-silico approach. Diabetes Technol. Ther. 19(1): A-128.
Satyavati, G.V., Raina, M.K. and Sharma, M. 1976. Medicinal Plants of India. ICMR, New Delhi.
Schmidt, C., Fronza, M., Goettert, M., Geller, F., Luik, S., Flores, E.M., Bittencourt, C.F., Zanetti, G.D.,
Heinzmann, B.M., Laufer, S. and Merfort, I. 2009. Biological studies on Brazilian plants used in
wound healing. J. Ethnopharmacol. 122(3): 523–532.
Siddiqui, H.H. 1993. Safety of herbal drugs—an overview. Drugs News & Views 1(2): 7–10.
Singh, N., Hoette, Y. and Miller, R. 2002. Tulsi: The mother medicine of nature. International Institute
of Herbal Medicine, Lucknow, India.
Singh, V., Birendra, V. and Suvagiya, V. 2011. A review on ethnomedical uses of Ocimum sanctum
(tulsi). Int. Res. J. Pharm. 2(10): 1–3.
Sirkar, N.N. 1989. Pharmacological basis of Ayurvedic therapeutics. In: Atal, C.K. and Kapoor, B.M.
(eds.). Cultivation and Utilization of Medicinal Plants. PID CSIR.
Sur, P.R., Sen, R., Halder, A.C. and Bandyopadhyay, S. 1987. Observation on the ethnobotany of Malda-
West Dinajpur districts, West Bengal-I. J. Econ. Tax. Bot. 10(2): 395–401.
Sur, P.R., Sen, R., Halder, A.C. and Bandyopadhyay, S. 1990. Observation on the ethnobotany of Malda-
West Dinajpur districts, West Bengal-II. J. Econ. Tax. Bot. 14(2): 453–459.
Sur, P.R., Sen, R. and Halder, A.C. 1992. Ethnobotanical study of Purulia district, West Bengal, India.
J. Econ. Taxon. Bot. Addl. Ser. 10: 259–264.
Talukdar, D. and Talukdar, T. 2012. Floral diversity and its indigenous use in old basin (Khari) of
river Atreyee at Balurghat block of Dakshin Dinajpur district, West Bengal. NeBIO 3(2): 26–32.
Talukdar, T. and Talukdar, D. 2013. Ethno-medicinal uses of plants by tribal communities in Hili block
of Dakshin Dinajpur district, West Bengal. Indian J. Nat. Prod. Resour. 4(1): 110–118.
Tiwari, A.K., Mishra, R. and Chaturvedi, A. 2014. Traditional uses of Ocimum sanctum (Tulsi). Int. J.
Glob. Sci. Res. 1(2): 126–131.
Ethnobotanical Study of Dakshin Dinajpur District of West Bengal—An Overview 157
Ulbricht, C.E. 2010. Natural standard: Herb and supplement guide—an evidence-based reference. St.
Louis, MO: Elsevier Mosby.
Upadhyaya, K.D. 1964. Indian botanical folklore. Asian Folkl Stud. 23(2): 15–34.
Warrier, P.K., Nambiar, V.P.K. and Ramankutty, C. 1995. A compendium of 500 species. pp 157–168.
In: Indian Medicinal Plants. Vol. 4. Orient Longman Publisher.
Xavier, T.F., Kannan, M., Lija, L., Auxillia, A., Rose, A.K.F. and Kumar, S.S. 2014. Ethnobotanical
study of Kani tribes in Thoduhills of Kerala, South India. J. Ethnopharmacol. 152(1): 78–90.
Yamashita, H., Tsukayama, H. and Sugishita, C. 2002. Popularity of complementary and alternative
medicine in Japan: A telephone survey. Complement Ther. Med. 10(2): 84–93.
CHAPTER 9
Introduction
Psoriasis is a chronic autoimmune inflammatory disease of the skin with a
worldwide prevalence of 2–3% (Nickoloff and Nestle 2004, Takeshita et al.
2017). The pathology is easy to recognize for the characteristic erythema, severe
inflammation, excessive proliferation of keratinocytes, and scaly plaques (Lowes
et al. 2007). In addition to the skin lesions, other associated pathologies could be
present, mainly nail dystrophy accompanied by psoriatic arthritis (20–25%), which
is similar to rheumatoid arthritis (Nickoloff and Nestle 2004). The pathogenesis of
these comorbid diseases remains unknown, but common inflammatory pathways,
cellular mediators, genetic susceptibility, and risk factors have been described as
contributing elements (Takeshita et al. 2017).
Nickoloff (1991) proposed a hypothesis for the pathophysiology of psoriasis,
in which a stimulus triggers a series of cellular events generating a cascade of
cytokines, such as tumor necrosis factor (TNF)-α derived from dendritic antigen-
presenting cells and keratinocytes, and interferon (IFN)-γ produced by activated
Th1 lymphocytes (Nickoloff 1991, Boehncke 2007). The evolution of psoriasis
treatment reflects the limitations in the knowledge of its pathogenesis. In the past,
treatments were based on serendipity and chance because neither the specific target
nor the mechanism of action for the treatment was known (Nickoloff and Nestle
2004). In this sense, arsenic (Fowler’s solution), ammoniated mercury, crude
1
Departament de Farmacologia, Facultat de Farmàcia, Universitat de València, Spain.
2
Facultad de Ciencias Médicas, Universidad Nacional de La Plata, CIC-PBA, Argentina.
3
FISABIO-Fundación Hospital Universitario Dr. Peset, Valencia, Spain.
4
Departamento de Ciencias Biomédicas, Universidad Europea de Valencia, Valencia, Spain.
* Corresponding author: [email protected]
Antipsoriatic Medicinal Plants: From Traditional Use to Clinic 159
coal tar, anthralin, corticosteroids and ultraviolet (UV)-B radiation have been
systematically used. The knowledge of the immunological components and some
relevant mediators implicated allowed the use of selective immunosuppressors
such as methotrexate, cyclosporine A, tacrolimus, psoralen + UV-A light therapy
(PUBA), fumaric acid esters, 5-aminolevulinic acid, 6-thioguanine, salicilates,
hydroxyurea and analogues of vitamins A (retinoids) and D. Advanced therapeutic
options include the use of biologic drugs which specifically target cytokines that
directly mediate the development of psoriasis, such as TNF-α inhibitors (etanercept,
infliximab, and adalimumab), anti-interleukin (IL)-12/IL-23 (ustekinumab) or
anti-IL-23 (secukinumab, ixekizumab) (Nickoloff and Nestle 2004, Herman and
Herman 2016).
Due to the side effects and elevated cost of the treatment of psoriasis with
these new biological drugs, patients often seek treatments outside the allopathic
paradigm (Shawahna and Jarada 2017). In different parts of the world, patients with
psoriasis employ medicinal plants and complementary and alternative medicine
(CAM) as a potential solution. Some medicinal plants are used topically but others
are administered orally for a systematic effect. Although the use of medicinal plants
is based on the traditional employ and, consequently, is not an evidence-based
practice, today different randomized clinical trials have been developed (Shawahna
and Jarada 2017). The use of CAM among patients with psoriasis is quite common
(43–69% prevalence), and the use of 1–6 herbs, special diets, or dietary supplements
are the most common processes (Smith et al. 2009, Tirant et al. 2018). The number
of randomized controlled clinical trials using different medicinal plants to treat
signs/symptoms of psoriasis are considerable, and the results are varied due to
cultural factors (Shawahna and Jarada 2017, Tirant et al. 2018).
The use of plant extracts or products as inhibitors of leukotriene synthesis is
based on the previous reports on the increase of lipoxygenase activity, leukotrienes
and other lipoxygenase products in the pathogenesis of psoriasis (Voorhees 1983).
Consequently, 5- and 12-lipoxygenase inhibitors could have beneficial effect
in this disease. Different pathologic events can be explained by the action of
12-hydroxyeicosatetraenoic acid (12-HETE): the normal epidermis synthesizes
predominantly 12(S)-HETE, whereas the product derived from psoriatic skin is its
enantiomer 12(R)-HETE (Schneider and Bucar 2005). However, Ford-Hutchinson
(1993) had previously described doubts on the case of 5-lipoxygenase because
there is no clear evidence of its presence in human skin, and selective leukotriene
biosynthesis inhibitors have no therapeutic utility in psoriasis. Based on these
features, many of the studied plants with potential as antipsoriatic agents are found
in the arachidonate metabolism via lipoxygenase and in their antioxidant properties.
applied to the skin or ingested before the patient was exposed to intense sunlight
(Seyger et al. 1998), but also other complementary and alternative medicines have
been used (Capella and Finzi 2003).
The first scientific report on the use of CAM in psoriatic patients was published
by Jensen in 1990, who compiled data on 215 patients with psoriasis based on a
questionnaire in Norway, which included different questions on the use of CAM.
The conclusion drawn from the questionnaire was that the absence of a satisfactory
effect of the standard therapy was the most decisive factor in using CAM, although,
as he reported, patient showed no improvement, or psoriasis was even aggravated
as a result of these alternative treatments (Jensen 1990a,b).
Amenta et al. (2000) compiled a series of 48 medicinal plants used around
the world for treating psoriasis, and 9 used specifically in Sicily (Italy). These
same authors indicated the extractive solvent and system for their application
(Table 9.1). More recently, Talbott and Duffy (2015) reviewed the efficacy of
herbal therapies against psoriasis and they observed the best efficacy in the case of
Berberis aquifolium (syn.: Mahonia aquifolium) and indigo naturalis, while it was
smaller for aloe (Aloe vera, syn: Aloe barbadensis), neem (Azadirachta indica),
and extracts of sweet whey. Indigo naturalis is a blue powder obtained from the
leaves of different plants, such as Strobilanthes cusia (syn.: Baphicacanthus cusia),
Persicaria tinctoria (syn.: Polygonum tinctorium), Isatis tinctoria (syn.: Isatis
indigotica) and Strobilanthes formosanus (McDermott et al. 2016). Herman and
Herman (2016) also compiled a series of studies of plants used against psoriasis.
All of them are included in Table 9.1. Some plant names have been modified and
the present name was introduced.
* All the plant names have been actualized according to the new taxonomic review cited in ‘The plant list. A working list of all plant species’: http://www.the-
plantlist.org/.
1
Aloe barbadensis Miller is a synonym of Aloe vera (L.) Burm.f.
2
Astragalus membranaceus (Fisch.) Bunge is a synonym of Astragalus propinquus Schischkin
3
Mahonia aquifolium (Pursh) Nutt. is a synonym of Berberis aquifolium Pursh.
4
Capsicum frutescens L. is a synonym of Capsicum annuum L.
5
Psoralea corylifolia L. is a synonym of Cullen corylifolium (L.) Medik
6
Curcuma wenyujin Y.H.Chen & C.Ling is a synonym of Curcuma aromatica Salisb.
7
Curcuma domestica Valeton is a synonym of Curcuma longa L.
8
Inula viscosa (L.) Aiton is a synonym of Dittrichia viscosa (L.) Greuter
9
Eruca sativa Mill. is a synonym of Eruca vesicaria (L.) Cav.
10
Sapium insigne (Royle) Trimen is a synonym of Falconeria insignis Royle
11
Givotia rottleriformis Griff. ex Wight is a synonym of Givotia moluccana (L.) Sreem
12
Tabebuia avellanedae Lorentz ex Griseb. is a synonym of Handroanthus impetiginosus (Mart. ex DC.) Mattos
13
Antipsoriatic Medicinal Plants: From Traditional Use to Clinic
Fig. 9.1. Chemical structures of madecassoside and asiaticoside. Gln = glucose; rha = rhamnose.
172 ETHNOBOTANY: Local Knowledge and Traditions
extracts on ten different genes of the NF-κB signaling network in HaCaT cells,
and observed that Thai ginger extract reduced the expression of NF-κB2, turmeric
extract significantly decreased the expression of both NF-κB2 and NF-κB1, while
Annona squamosa extract significantly lowered the expression of NF-κB1. So, this
in vitro study suggested that these medicinal plants might exert their antipsoriatic
activity by controlling the expression of NF-κB signaling biomarkers.
Other relevant mediators in psoriasis are matrix metalloproteinases (MMP),
and its inhibition by Scrophularia striata extract and some isolated compounds
were studied by Monsef-Esfahani et al. (2014). Among these isolated compounds,
the inhibitory effects of nepitrin at 20 µg/mL (56%) and acteoside at 80 µg/mL
(73%) on MMP-2 and MMP-9 were remarkable. Lipoxygenase and elastase could
also be potential therapeutic targets in psoriasis. In this sense, Prieto et al. (2003)
screened 15 extracts from traditional Chinese medicinal plants/fungi used to treat
topical inflammations such as psoriasis. They were screened for their inhibitory
effect on lipoxygenase, cyclooxygenase and elastase activity in intact leukocytes
and platelets. Astragalus propinquus (syn: Astragalus membranaceus), Forsythia
suspensa and Wolfiporia extensa (syn: Poria cocos) inhibited 5-lipoxygenase (IC50
values of 141, 80 and 141 µg/mL, respectively). Angelica dahurica, Angelica
pubescens, F. suspensa and W. extensa also inhibited elastase (IC50 values of 80, 123,
68 and 93 µg/mL, respectively). Previously, Cuéllar et al. (1996) had demonstrated
the inhibitory effect of W. extensa extract and its metabolites dehydrotumulosic and
pachymic acids on phospholipase A2 activity as well as experimental dermatitis
(Cuéllar et al. 1997).
The metabolism of arachidonic acid via lipoxygenase enzymes, 5-, 12- and
15-lipoxygenases has been highlighted as the potential target for antipsoriatic
treatments. The 5-lipoxygenase pathway is considered important since it participates
in pro-inflammatory regulations, but the 12- and 15-lipoxygenase pathway may
also play an important role in the progression of psoriasis (Schneider and Bucar
2005). Bader et al. (2015) tested four species used in Southern Italy for the treatment
of psoriasis against 5-, 12-, 15-lipoxygenase and NF-κB activation: Acanthus
mollis, Achillea ligustica, Artemisia arborescens and Dittrichia viscosa (syn:
Inula viscosa). According to their results, the effect of A. ligustica was the most
relevant as it had the highest anti-5-lipoxygenase activity (IC50 = 49.5 µg/mL) and
also enhanced the biosynthesis of the anti-inflammatory eicosanoid 15(S)-HETE.
These species also reduced the activation of NF-κB, having IC50 values of 16.7,
19.2 and 30.4 μg/mL for A. ligustica, A. arborescens and D. viscosa, respectively.
Nagar et al. (2016) tested the in vivo activity of Woodfordia fructicosa and
Gardenia gummifera on a psoriasis model induced in Wistar rats: 10% of total
body area was exposed to UV radiations after topical (0.1% gel of the extract) and
oral (dose of 100 mg/kg) administration. The antipsoriatic activity (severity index),
histological analysis and biochemical estimation suggest positive antipsoriatic
effects of both plant extracts. Other interesting species against psoriasis could be
Tinospora sinensis, Curcuma longa, Celastrus paniculatus, and Aloe vera, which
were tested in a model of psoriasis-like dermatitis using topical application of 5%
Antipsoriatic Medicinal Plants: From Traditional Use to Clinic 173
in vitro, gambogic acid inhibited the proliferation of the human keratinocyte cell
line HaCaT (IC50 = 0.09 µM) and it was also demonstrated to be active in human
umbilical vein endothelial cells (HUVEC) by inhibiting TNF-α-induced activation
of NF-κB, both processes being highly active in psoriatic patients. Honokiol also
inhibited TNF-α-induced NF-κB activation in HUVEC and decreased the ratio of
Th1/Th2-expression CD4+ T cells.
Gambogic acid and honokiol were also demonstrated to be effective in vivo.
K14-VEGF transgenic mice with moderate psoriasis treated with gambogic acid
showed a reduction in the erythema, resolution of the epidermal hyperplasia and
acanthosis, decreased parakeratosis with reduced inflammatory infiltrate and
reduced vascular hyperplasia and inflammation (evidenced by reduced expression of
adhesion molecules such as E-selectin and ICAM-1). In the case of honokiol, it also
normalized the psoriatic phenotype in K14-VEGF mice, producing macroscopic and
histologic improvement, and dose-dependently decreased TNF-α and IFN-γ levels,
this reduction being associated with suppression of p65-NF-κB expression in the
ear tissues analyzed. Both gambogic acid and honokiol inhibited angiogenesis and
the expression of vascular endothelial growth factor-2 (VEGF2) and p-VEGFR2
and, in the case of honokiol, this inhibition was accompanied by suppression of
phosphorylation of extracellular signal–regulated kinase1/2 (ERK1/2), protein
kinase B (AKT) and p38 mitogen-activated protein kinase (p38 MAPK). Gambogic
acid was tested in a second animal model: a psoriasis-like model of guinea-pig,
where improvements in epidermis and dermic could be detected (Wen et al. 2014a).
Paeoniflorin (Fig. 9.3), a monoterpene glycoside isolated from paeony root
(Paeonia lactiflora), has also been tested in this psoriasis-like model of guinea-
pig, where it relieved the lesions improving parakeratosis and hyperkeratinization.
Antipsoriatic Medicinal Plants: From Traditional Use to Clinic 175
In vitro, in HaCaT cells, it inhibits the expression of IL-17A, and IL-22 (2.08 µM)
through a mechanism involving p38 MAPK (Yu et al. 2017).
Celastrol (Fig. 9.3) is also a terpenoid isolated from Celastrus orbiculatus.
This herb has been traditionally used in Chinese medicine for anti-inflammatory,
anti-cancer and antioxidant activities, especially in the treatment of rheumatoid
arthritis and skin diseases. Zhou et al. (2011) demonstrated that this triterpene is
able to inhibit HaCaT growth (IC50 = 1.1 µM) and induce their apoptosis through
the inhibition of NF-κB pathway.
Alkaloids with described antipsoriatic properties can be found in Berberis
aquifolium, whose bark has been traditionally used in North America for the
treatment of several skin diseases, including psoriasis, and are mostly active in the
lipoxygenase metabolism (Müller and Ziereis 1993, Misik et al. 1995, Bezáková
et al. 1996). Berberis aquifolium extract inhibits the production of LTB4 and
5-HETE (IC50 = 50 µM) in isolated bovine polymorphonuclear cells (Müller and
Ziereis 1993), although the authors could not explain this effect by the action of the
studied alkaloids berberine, oxyacanthine and berbamine. None of the three were
as effective in inhibiting lipid peroxidation as the whole extract, although these
alkaloids did show some antioxidant effect (much less than the whole extract). In
this sense, protoberberine alkaloids (berberine, oxyberberine, jatrorrhizine, and
176 ETHNOBOTANY: Local Knowledge and Traditions
Columbamine
Oxyberberine
IL-6, IL17A, IL-17F, and IL-22) through a mechanism involving NF-κB inhibition
(Sun et al. 2013), whilst resveratrol (Fig. 9.6) inhibits the expression of IL-17A,
IL-19, and IL-23p19 (Kjær et al. 2015). Quercetin (Fig. 9.6) caused a reduction in
the levels of TNF-α, IL-6 and IL-17 in serum, increased the activities of glutathione,
catalase and superoxide dismutase, and decreased the skin accumulation of
malonaldehyde through a mechanism which involved the downregulation of the
NF-κB pathway (Chen et al. 2017).
Clinical Trials
In traditional Chinese medicine (TCM), the application of medicinal plants has been
used for centuries in the management of psoriasis and is believed to be effective, with
few long-term side-effects (Koo and Arain 1998). Psoriasis is commonly classified
into three main syndromes in TCM: ‘blood heat’, ‘blood dryness’ and ‘blood stasis’,
and different medicinal plants are used to fight these conditions and restore the
balanced state of the body (Tse 2003). However, the number of clinical trial dealing
with medicinal plants in the treatment of psoriasis is quite limited (Table 9.2) and
show big differences in their design, number of participants, parameters evaluated
and form of treatment. It is worth noting that clinical trials evaluating ‘indigo
naturalis’ are the most numerous and results conclude that its topical application
is a safe and effective therapy for plaque-type psoriasis and nail psoriasis.
Regarding the species contained in the clinical trials revised, Paeonia lactiflora
and Smilax glabra are the most commonly studied. Paeoniae radix and smilacis
glabrae rhizoma are two of the most well-known herbs in China and have been
used for over 1200 years. Both species have been tested in different experimental
models of inflammation and immunomodulation with excellent results (Spelman
et al. 2006, He and Dai 2011). Other species of interest for treating psoriasis
are Aloe vera (Miroddi et al. 2015) and Berberis aquifolium (Jong et al. 2013).
The quality of the trials and methodological approaches vary considerably, and
conclusions on the effectiveness of aloe in psoriasis is still uncertain. Cutaneous
application seems to be very safe as serious side effects have not been reported.
Antipsoriatic Medicinal Plants: From Traditional Use to Clinic 179
Table 9.2. Clinical trials of traditional Chinese medicines used in the treatment of psoriasis.
Conclusions
The majority of medicinal plants used in the treatment of psoriasis are based on
their traditional use and folk medicine, without relevant studies on humans. The
number of clinical trials is limited and, those available, are not clearly defined, the
number of patients is limited and the evaluation of results is variable. Moreover,
some of these trials involve mixtures of plants (Deng et al. 2017, Na Takuathung et
al. 2017) or use them simultaneously with standard drugs, such as calcipotriol and
betamethasone (Wen et al. 2014b), which hinders their evaluation. Nevertheless,
many of these plants still have potential as antipsoriatic drugs. Among these, the
species studied with a high level of interest include Aloe vera, Paeonia lactiflora,
Smilax glabra—which improves the psoriatic plaques by 83% and PASI score by
83% vs. placebo—and Berberis aquifolium. Phlebodium decumanum, Camptotheca
acuminata, Oldenlandia diffusa, Rehmannia glutinosa and Salvia miltiorrhiza
are also remarkable since they have the three pharmacological activities which
182 ETHNOBOTANY: Local Knowledge and Traditions
References
Amenta, R., Camarda, L., Di Stefano, V., Lentini, F. and Venza, F. 2000. Traditional medicine as a source
of new therapeutic agents against psoriasis. Fitoterapia. 71(Suppl. 1): S13−S20.
Arora, N., Shah, K. and Pandey-Rai, S. 2016. Inhibition of imiquimod-induced psoriasis-like dermatitis
in mice by herbal extracts from some Indian medicinal plants. Protoplasma. 253: 503−515.
Augustin, M., Andrees, U., Grimme, H., Schöpf, E. and Simon, J. 1999. Effects of Mahonia aquifolium
ointment on the expression of adhesion, proliferation, and activation markers in the skin of patients
with psoriasis. Forsch. Komplementarmed. 6(Suppl. 2): 19−21.
Bader, A., Martini, F., Schinella, G.R., Ríos, J.L. and Prieto, J.M. 2015. Modulation of COX-1, 5-,
12- and 15-LOX by popular herbal remedies used in southern Italy against psoriasis and other
skin diseases. Phytother. Res. 29: 108−113.
Bezáková, L., Misik, V., Máleková, L., Svajdlenka, E. and Kostálová, D. 1996. Lipoxygenase inhibition
and antioxidant properties of bisbenzylisoquinoline alkaloids isolated from Mahonia aquifolium.
Pharmazie. 51: 758−761.
Boehncke, W.H. 2007. Efalizumab in the treatment of psoriasis. Biologics. 1: 301−309.
Brown, A.C., Koett, J., Johnson, D.W., Semaskvich, N.M., Holck, P., Lally, D., Cruz, L., Young, R.,
Higa, B. and Lo, S. 2005. Effectiveness of kukui nut oil as a topical treatment for psoriasis. Int.
J. Dermatol. 44: 684−687.
Capella, G.L. and Finzi, A.F. 2003. Complementary therapy for psoriasis. Dermatol. Ther. 16: 164−174.
Carrenho, L.Z., Moreira, C.G., Vandresen, C.C., Gomes Junior, R., Gonçalves, A.G., Barreira, S.M.,
Noseda, M.D., Duarte, M.E., Ducatti, D.R., Dietrich, M., Paludo, K., Cabrini, D.A. and Otuki,
M.F. 2015. Investigation of anti-inflammatory and anti-proliferative activities promoted by
photoactivated cationic porphyrin. Photodiagnosis Photodyn. Ther. 12: 444−458.
Chen, H., Lu, C., Liu, H., Wang, M., Zhao, H., Yan, Y. and Han, L. 2017. Quercetin ameliorates
imiquimod-induced psoriasis-like skin inflammation in mice via the NF-κB pathway. Int.
Immunopharmacol. 48: 110−117.
Cheng, H.M., Wu, Y.C., Wang, Q., Song, M., Wu, J., Chen, D., Li, K., Wadman, E., Kao, S.T., Li,
T.C., Leon, F., Hayden, K., Brodmerkel, C. and Chris Huang, C. 2017. Clinical efficacy and
IL-17 targeting mechanism of Indigo naturalis as a topical agent in moderate psoriasis. BMC
Complement. Altern. Med. 17: 439.
Choi, M.R., Choi, D.K., Sohn, K.C., Lim, S.K., Kim, D.I., Lee, Y.H., Im, M., Lee, Y., Seo, Y.J., Kim,
C.D. and Lee, J.H. 2015. Inhibitory effect of Paeonia lactiflora Pallas extract (PE) on poly (I:C)-
induced immune response of epidermal keratinocytes. Int. J. Clin. Exp. Pathol. 8: 5236−5241.
Cuéllar, M.J., Giner, R.M., Recio, M.C., Just, M.J., Máñez, S. and Ríos, J.L. 1996. Two fungal lanostane
derivatives as phospholipase A2 inhibitors. J. Nat. Prod. 59: 977−979.
Cuéllar, M.J., Giner, R.M., Recio, M.C., Just, M.J., Máñez, S. and Ríos, J.L. 1997. Effect of the
basidiomycete Poria cocos on experimental dermatitis and other inflammatory conditions. Chem.
Pharm. Bull. (Tokyo) 45: 492−494.
Dai, Y.J., Li, Y.Y., Zeng, H.M., Liang, X.A., Xie, Z.J., Zheng, Z.A., Pan, Q.H. and Xing, Y.X. 2014.
Effect of Yinxieling decoction on PASI, TNF-α and IL-8 in patients with psoriasis vulgaris. Asian
Pac. J. Trop. Med. 7: 668−670.
Deng, S., May, B.H., Zhang, A.L., Lu, C. and Xue, C.C. 2013a. Plant extracts for the topical management
of psoriasis: a systematic review and meta-analysis. Br. J. Dermatol. 169: 769−782.
Deng, S., May, B.H., Zhang, A.L., Lu, C. and Xue, C.C. 2013b. Topical herbal medicine combined
with pharmacotherapy for psoriasis: a systematic review and meta-analysis. Arch. Dermatol.
Res. 305: 179−189.
Deng, S., May, B.H., Zhang, A.L., Lu, C. and Xue, C.C. 2014. Phytotherapy in the management of
psoriasis: a review of the efficacy and safety of oral interventions and the pharmacological actions
of the main plants. Arch. Dermatol. Res. 306: 211−229.
Antipsoriatic Medicinal Plants: From Traditional Use to Clinic 183
Deng, J., Yao, D., Lu, C., Wen, Z., Yan, Y., He, Z., Wu, H. and Deng, H. 2017. Oral Chinese herbal
medicine for psoriasis vulgaris: protocol for a randomised, double-blind, double-dummy,
multicentre clinical trial. BMJ Open 7: e014475.
Di Nardo, V., Gianfaldoni, S., Tchernev, G., Wollina, U., Barygina, V., Lotti, J., Daaboul, F. and Lotti,
T. 2018. Use of curcumin in psoriasis. Open Access Maced. J. Med. Sci. 6: 218−220.
Ford-Hutchinson, A.W. 1993. 5-Lipoxygenase activation in psoriasis: a dead issue? Skin. Pharmacol.
6: 292−297.
He, D.Y. and Dai, S.M. 2011. Anti-inflammatory and immunomodulatory effects of Paeonia lactiflora
Pall., a traditional Chinese herbal medicine. Front. Pharmacol. 2: 10.
Herman, A. and Herman, A.P. 2016. Topically used herbal products for the treatment of psoriasis—
Mechanism of action, drug delivery, clinical studies. Planta Med. 82: 1447−1455.
Jensen, P. 1990a. Use of alternative medicine by patients with atopic dermatitis and psoriasis. Acta
Derm. Venereol. 70: 421−424.
Jensen, P. 1990b. Alternative therapy for atopic dermatitis and psoriasis: patient-reported motivation,
information source and effect. Acta Derm. Venereol. 70: 425−428.
Jong, M.C., Ermuth, U. and Augustin, M. 2013. Plant-based ointments versus usual care in the
management of chronic skin diseases: a comparative analysis on outcome and safety. Complement.
Ther. Med. 21: 453−459.
Kaur, A. and Kumar, S. 2012. Plants and plant products with potential antipsoriatic activity—a review.
Pharm. Biol. 50: 1573−1591.
Kjær, T.N., Thorsen, K., Jessen, N., Stenderup, K. and Pedersen, S.B. 2015. Resveratrol ameliorates
imiquimod-induced psoriasis-like skin inflammation in mice. PLoS One 10: e0126599.
Koo, J. and Arain, S. 1998. Traditional Chinese medicine for the treatment of dermatologic disorders.
Arch. Dermatol. 134: 1388−1393.
Lee, S.Y., Nam, S., Hong, I.K., Kim, H., Yang, H. and Cho, H.J. 2018. Antiproliferation of keratinocytes
and alleviation of psoriasis by the ethanol extract of Artemisia capillaris. Phytother Res. doi:
10.1002/ptr.6032.
Li, N., Zhao, W., Xing, J., Liu, J., Zhang, G., Zhang, Y., Li, Y., Liu, W., Shi, F. and Bai, Y. 2017. Chinese
herbal Pulian ointment in treating psoriasis vulgaris of blood-heat syndrome: a multi-center,
double-blind, randomized, placebo-controlled trial. BMC Complement. Altern. Med. 17: 264.
Liu, H.P., Liu, H.C. and Li, G.Y. 2001. Integrated traditional Chinese and western medicine in treating
37 psoriatic patients. Chin. J. Integr. Med. 7: 53.
Lin, Y.K., Yen, H.R., Wong, W.R., Yang, S.H. and Pang, J.H. 2006. Successful treatment of pediatric
psoriasis with indigo naturalis composite ointment. Pediatr. Dermatol. 23: 507−510.
Lin, Y.K., Chang, C.J., Chang, Y.C., Wong, W.R., Chang, S.C. and Pang, J.H. 2008. Clinical assessment
of patients with recalcitrant psoriasis in a randomized, observer-blind, vehicle-controlled trial
using indigo naturalis. Arch. Dermatol. 144: 1457−1464.
Lin, Y.K., See, L.C., Huang, Y.H., Chang, Y.C., Tsou, T.C., Leu, Y.L. and Shen, Y.M. 2012. Comparison
of refined and crude indigo naturalis ointment in treating psoriasis: Randomized, observer-blind,
controlled, intrapatient trial. Arch. Dermatol. 148: 397−400.
Lin, Y.K., See, L.C., Huang, Y.H., Chang, Y.C., Tsou, T.C., Lin, T.Y. and Lin, N.L. 2014. Efficacy and
safety of indigo naturalis extract in oil (Lindioil) in treating nail psoriasis: a randomized, observer-
blind, vehicle-controlled trial. Phytomedicine 21: 1015−1020.
Lin, Y.K., Chang, Y.C., Hui, R.C., See, L.C., Chang, C.J., Yang, C.H. and Huang, Y.H. 2015. A Chinese
herb, indigo naturalis, extracted in oil (Lindioil) used topically to treat psoriatic nails: a randomized
clinical trial. JAMA Dermatol. 151: 672−674.
Lowes, M.A., Bowcock, A.M. and Krueger, J.G. 2007. Pathogenesis and therapy of psoriasis. Nature.
445: 866−873.
Lu, C., Liu, H., Jin, X., Chen, Y., Liang, C.L., Qiu, F. and Dai, Z. 2018. Herbal components of
a novel formula PSORI-CM02 interdependently suppress allograft rejection and induce
CD8+CD122+PD-1+ regulatory T cells. Front. Pharmacol. 9: 88.
Mansouri, P., Mirafzal, S., Najafizadeh, P., Safaei-Naraghi, Z., Salehi-Surmaghi, M.H. and Hashemian,
F. 2017. The impact of topical Saint John’s Wort (Hypericum perforatum) treatment on tissue tumor
necrosis factor-alpha levels in plaque-type psoriasis: A pilot study. J. Postgrad. Med. 63: 215−220.
184 ETHNOBOTANY: Local Knowledge and Traditions
McDermott, L., Madan, R., Rupani, R. and Siegel, D. 2016. A review of indigo naturalis as an alternative
treatment for nail psoriasis. J. Drugs Dermatol. 15: 319−323.
Miroddi, M., Navarra, M., Calapai, F., Mancari, F., Giofrè, S.V., Gangemi, S. and Calapai, G. 2015.
Review of clinical pharmacology of Aloe vera L. in the treatment of psoriasis. Phytother. Res.
29: 648−655.
Misík, V., Bezáková, L., Máleková, L. and Kostálová, D. 1995. Lipoxygenase inhibition and antioxidant
properties of protoberberine and aporphine alkaloids isolated from Mahonia aquifolium. Planta
Med. 61: 372−373.
Monsef-Esfahani, H.R., Shahverdi, A.R., Khorramizadeh, M.R., Amini, M. and Hajiaghaee, R. 2014.
Two matrix metalloproteinase inhibitors from Scrophularia striata Boiss. Iran. J. Pharm. Res.
13: 149−155.
Müller, K. and Ziereis, K. 1993. Effects of oxygen radicals, hydrogen peroxide and water-soluble singlet
oxygen carriers on 5- and 12-lipoxygenase. Arch. Pharm. (Weinheim). 326: 819−821.
Müller, K., Ziereis, K. and Gawlik, I. 1995. The antipsoriatic Mahonia aquifolium and its active
constituents; II. Antiproliferative activity against cell growth of human keratinocytes. Planta
Med. 61: 7475.
Muruganantham, N., Basavaraj, K.H., Dhanabal, S.P., Praveen, T.K., Shamasundar, N.M. and Rao,
K.S. 2011. Screening of Caesalpinia bonduc leaves for antipsoriatic activity. J. Ethnopharmacol.
133: 897−901.
Na Takuathung, M., Wongnoppavich, A., Pitchakarn, P., Panthong, A., Khonsung, P., Chiranthanut,
N., Soonthornchareonnon, N. and Sireeratawong, S. 2017. Effects of Wannachawee Recipe
with antipsoriatic activity on suppressing inflammatory cytokine production in HaCaT human
keratinocytes. Evid. Based Complement. Alternat. Med. 2017: 5906539.
Nagar, H.K., Srivastava, A.K., Srivastava, R. and Ranawat, M.S. 2016. Evaluation of potent
phytomedicine for treatment of psoriasis using UV radiation induced psoriasis in rats. Biomed.
Pharmacother. 84: 1156−1162.
Nickoloff, B.J. 1991. The cytokine network in psoriasis. Arch. Dermatol. 127: 871–884.
Nickoloff, B.J. and Nestle, F.O. 2004. Recent insights into the immunopathogenesis of psoriasis provide
new therapeutic opportunities. J. Clin. Invest. 113: 1664−1675.
Parker, S., Zhang, A.L., Zhang, C.S., Goodman, G., Wen, Z., Lu, C. and Xue, C.C. 2014. Oral granulated
Chinese herbal medicine (YXBCM01) plus topical calcipotriol for psoriasis vulgaris: study protocol
for a double-blind, randomized placebo controlled trial. Trials 15: 495.
Prieto, J.M., Recio, M.C., Giner, R.M., Máñez, S., Giner-Larza, E.M. and Ríos, J.L. 2003. Influence
of traditional Chinese anti-inflammatory medicinal plants on leukocyte and platelet functions.
J. Pharm. Pharmacol. 55: 1275−1282.
Saelee, C., Thongrakard, V. and Tencomnao, T. 2011. Effects of Thai medicinal herb extracts with
anti-psoriatic activity on the expression on NF-κB signaling biomarkers in HaCaT keratinocytes.
Molecules 16: 3908−3932.
Sampson, J.H., Raman, A., Karlsen, G., Navsaria, H. and Leigh, I.M. 2001. In vitro keratinocyte
antiproliferant effect of Centella asiatica extract and triterpenoid saponins. Phytomedicine
8: 230−235.
Schneider, I. and Bucar, F. 2005. Lipoxygenase inhibitors from natural plant sources. Part 2: medicinal
plants with inhibitory activity on arachidonate 12-lipoxygenase, 15-lipoxygenase and leukotriene
receptor antagonists. Phytother. Res. 19: 263−272.
Sethi, G., Sung, B., Kunnumakkara, A.B. and Aggarwal, B.B. 2009. Targeting TNF for treatment of
cancer and autoimmunity. Adv. Exp. Med. Biol. 647: 37−51.
Seyger, M.M., van de Kerkhof, P.C., van Vlijmen-Willems, I.M., de Bakker, E.S., Zwiers, F. and de
Jong, E.M. 1998. The efficacy of a new topical treatment for psoriasis: Mirak. J. Eur. Acad.
Dermatol. Venereol. 11: 13−18.
Shan, C., Yuan, L., Xiuzhen, B. and Aiju, Q. 2006. Treatment of psoriasis vulgaris by oral administration
of yin xie ping granules—a clinical report of 60 cases. J. Tradit. Chin. Med. 26: 198−201.
Shawahna, R. and Jaradat, N.A. 2017. Ethnopharmacological survey of medicinal plants used by patients
with psoriasis in the West Bank of Palestine. BMC Complement. Altern. Med. 17: 4.
Antipsoriatic Medicinal Plants: From Traditional Use to Clinic 185
Simpson, B.S., Luo, X., Costabile, M., Caughey, G.E., Wang, J., Claudie, D.J., McKinnon, R.A. and
Semple, S.J. 2014. Polyandric acid A, a clerodane diterpenoid from the Australian medicinal
plant Dodonaea polyandra, attenuates pro-inflammatory cytokine secretion in vitro and in vivo.
J. Nat. Prod. 77: 85−91.
Singh, K.K. and Tripathy, S. 2014. Natural treatment alternative for psoriasis: a review on herbal
resources. J. Appl. Pharm. Sci. 4: 114−121.
Singh, S.K., Chouhan, H.S., Sahu, A.N. and Narayan, G. 2015. Assessment of in vitro antipsoriatic
activity of selected Indian medicinal plants. Pharm. Biol. 53: 1295−1301.
Smith, N., Weymann, A., Tausk, F.A. and Gelfand, J.M. 2009. Complementary and alternative medicine
for psoriasis: a qualitative review of the clinical trial literature. J. Am. Acad. Dermatol. 61: 841−856.
Song, P., Lysvand, H., Yuhe, Y., Liu, W. and Iversen, O.J. 2010. Expression of the psoriasis-associated
antigen, Pso p27, is inhibited by traditional Chinese medicine. J. Ethnopharmacol. 127: 171−174.
Spelman, K., Burns, J., Nichols, D., Winters, N., Ottersberg, S. and Tenborg, M. 2006. Modulation
of cytokine expression by traditional medicines: a review of herbal immunomodulators. Altern.
Med. Rev. 11: 128−150.
Sun, J., Zhao, Y. and Hu, J. 2013. Curcumin inhibits imiquimod-induced psoriasis-like inflammation
by inhibiting IL-1beta and IL-6 production in mice. PLoS One 8: e67078.
Syed, T.A., Ahmad, S.A., Holt, A.H., Ahmad, S.A., Ahmad, S.H. and Afzal, M. 1996. Management of
psoriasis with Aloe vera extract in a hydrophilic cream: a placebo-controlled, double-blind study.
Trop. Med. Int. Health. 1: 505−509.
Takeshita, J., Grewal, S., Langan, S.M., Mehta, N.N., Ogdie, A., Van Voorhees, A.S. and Gelfand, J.M.
2017. Psoriasis and comorbid diseases: Epidemiology. J. Am. Acad. Dermatol. 76: 377−390.
Talbott, W. and Duffy, N. 2015. Complementary and alternative medicine for psoriasis: what the
dermatologist needs to know. Am. J. Clin. Dermatol. 16: 147−165.
Tian, Q., Li, J., Xie, X., Sun, M., Sang, H., Zhou, C., An, T., Hu, L., Ye, R.D. and Wang, M.W. 2005.
Stereospecific induction of nuclear factor-κB activation by isochamaejasmin. Mol. Pharmacol.
68: 1534−1342.
Tirant, M., Lotti, T., Gianfaldoni, S., Tchernev, G., Wollina, U. and Bayer, P. 2018. Integrative
dermatology—the use of herbals and nutritional supplements to treat dermatological conditions.
Open Access Maced. J. Med. Sci. 6: 185−202.
Tse, T.W. 2003. Use of common Chinese herbs in the treatment of psoriasis. Clin. Exp. Dermatol. 28:
469−475.
Tuominen, M., Bohlin, L. and Rolfsen, W. 1992. Effects of calaguala and an active principle, adenosine,
on platelet activating factor. Planta Med. 58: 306−310.
van der Fits, L., Mourits, S., Voerman, J.S., Kant, M., Boon, L., Laman, J.D., Cornelissen, F., Mus,
A.M., Florencia, E., Prens, E.P. and Lubberts, E. 2009. Imiquimod-induced psoriasis-like skin
inflammation in mice is mediated via the IL-23/IL-17 axis. J. Immunol. 182: 5836−5845.
Vasänge, M., Rolfsen, W. and Bohlin, L. 1997. A sulphonoglycolipid from the fern Polypodium
decumanum and its effect on the platelet activating-factor receptor in human neutrophils.
J. Pharm. Pharmacol. 49: 562−566.
Vasänge-Tuominen, M., Perera-Ivarsson, P., Shen, J., Bohlin, L. and Rolfsen, W. 1994. The fern
Polypodium decumanum, used in the treatment of psoriasis, and its fatty acid constituents as
inhibitors of leukotriene B4 formation. Prostaglandins Leukot. Essent. Fatty Acids 50: 279−284.
Venkatesha, S.H. and Moudgil, K.D. 2016. Celastrol and its role in controlling chronic diseases. Adv.
Exp. Med. Biol. 928: 267−289.
Vogler, B.K. and Ernst, E. 1999. Aloe vera: a systematic review of its clinical effectiveness. Br. J. Gen.
Pract. 49: 823−828.
Voorhees, J.J. 1983. Leukotrienes and other lipoxygenase products in the pathogenesis and therapy of
psoriasis and other dermatoses. Arch. Dermatol. 119: 541−547.
Wen, J., Pei, H., Wang, X., Xie, C., Li, S., Huang, L., Qiu, N., Wang, W., Cheng, X. and Chen, L.
2014a. Gambogic acid exhibits anti-psoriatic efficacy through inhibition of angiogenesis and
inflammation. J. Dermatol. Sci. 74: 242−250.
186 ETHNOBOTANY: Local Knowledge and Traditions
Wen, Z.H., Xuan, M.L., Yan, Y.H., Li, X.Y., Yao, D.N., Li, G., Guo, X.F., Ou, A.H. and Lu, C.J. 2014b.
Chinese medicine combined with calcipotriol betamethasone and calcipotriol ointment for psoriasis
vulgaris (CMCBCOP): study protocol for a randomized controlled trial. Trials 15: 294.
Wen, J., Wang, X., Pei, H., Xie, C., Qiu, N., Li, S., Wang, W., Cheng, X. and Chen, L. 2015. Anti-
psoriatic effects of honokiol through the inhibition of NF-κB and VEGFR-2 in animal model of
K14-VEGF transgenic mouse. J. Pharmacol. Sci. 128: 116124.
Yao, D.N., Lu, C.J., Wen, Z.H., Yan, Y.H., Xuan, M.L., Li, X.Y., Li, G., He, Z.H., Xie, X.L., Deng,
J.W., Guo, X.F. and Ou, A.H. 2016. Oral PSORI-CM01, a Chinese herbal formula, plus topical
sequential therapy for moderate-to-severe psoriasis vulgaris: pilot study for a double-blind,
randomized, placebo-controlled trial. Trials 17: 140.
Yu, J., Xiao, Z., Zhao, R., Lu, C. and Zhang, Y. 2017. Paeoniflorin suppressed IL-22 via p38 MAPK
pathway and exerts anti-psoriatic effect. Life Sci. 180: 17−22.
Zhou, L.L., Lin, Z.X., Fung, K.P., Cheng, C.H.K., Che, C.T., Zhao, M., Wu, S.H. and Zuo, Z. 2011.
Celastrol-induced apoptosis in human HaCaT keratinocytes involves the inhibition of NF-κB
activity. Eur. J. Pharmacol. 670: 399−408.
CHAPTER 10
Knowledge of the
Ethnomedicinal Plants Used
by Tobas and Mocovíes Tribes in
the Central-North of Argentina
María I. Stegmayer,1 Norma H. Alvarez,1 Melina G. Di Liberto,2
Lucas D. Daurelio1 and Marcos G. Derita1,2,*
Introduction
Among the flora of different regions of the world, Latin America represents one
of the wealthiest sources of material with pharmacological activities due to its
biodiversity (Brandão et al. 2008). It possesses a very high number of vascular
plants (85,000) (Grornbridge 1992) and there is a recent evidence that neotropical
forests located in Latin America possess the highest diversity of plants in the world
(Berry 2002). In addition, some factors critically distinguish the medicinal plants
of Latin America: (1) this region possesses a huge unexplored biodiversity (Cruz et
al. 2007); (2) there is a rich traditional use of medicinal plants (Gupta 1995, 2008);
(3) the ethnopharmacological knowledge has been tightly kept or transmitted by the
many indigenous populations still living in this region (Murillo 1889, Rosenblat
1954, Morton 1981, Correia 1984, Cleaves 2001, Portillo et al. 2001, Coelho de
1
CONICET, Universidad Nacional del Litoral/Facultad de Ciencias Agrarias/Laboratorio de
Investigaciones en Fisiología y Biología Molecular Vegetal, Kreder 2805, Esperanza, Santa Fe,
Argentina.
2
CONICET, Universidad Nacional de Rosario/Facultad de Ciencias Bioquímicas y Farmacéuticas/
Cátedra de Farmacognosia, Suipacha 531, Rosario, Santa Fe, Argentina.
* Corresponding author: [email protected]
188 ETHNOBOTANY: Local Knowledge and Traditions
Souza et al. 2004, Scarpa 2004a, Goleniowski et al. 2006, Cruz et al. 2007, Estévez
et al. 2007); and (4) these resources have been poorly studied.
In Argentina, there is a large number of indigenous people living in different
communities that are present in several geographical areas, each one with its
own cultural characteristics. During the 200 years of history of the nation, these
populations were victims of all kinds of physical and symbolic violence by the
ruling classes, overwhelming their customs and lifestyles. They were exiled from
their territories and forced to assume a religion and social norms, which were
completely alien to them. However, some tribes maintained their identity and still
endure, although they had to adapt to new living conditions in large cities.
Many studies on the medical folklore of northwestern Argentina (Di Lullo
1929, 1946, Sosa Verón and Vivante 1951, Daoud 1954, Ávila 1960, Carrizo 1960,
Torres 1975) are of great ethnographical value as they unravel ancient therapeutic
practices, many of which have been lost. However, these studies are incomplete in
their review of plants and the medicinal uses related to them. Later studies carried
out by Sturzenegger (1987, 1989, 1999) focusing on medical anthropology do not
provide enough information on medicinal plants either. Finally, Scarpa (2000)
points out 81 uses of 61 plant species in veterinary medicine by the Hispano-
Quechua community called “Criollo” groups. He also showed that their veterinary
health practices involve different approaches to treatment: the ancient Hippocratic
medicine, magical procedures and Christian religious practices. Healing with
plant remedies is not a specialized activity within this society. As with most folk
knowledge, it is mainly well spread within the population. When Criollos fall ill,
they resort to the experience of an elderly member of the community with a good
knowledge about home remedies. For unknown diseases or when home remedies
fail, they resort to the nearest village hospital for treatment or, alternatively, to
somebody who “cures by secret”. The latter, called “curanderos” (medicine-man),
are endowed with a gift known as “the secret”; they carry out a special therapy
by invoking supernatural forces. These therapies are performed by rituals called
“cura de palabra” (healing by words) and “cura por el rastro” (healing through
traces) which involve magical and/or religious elements such as spells, prayers, or
invocations to God and/or saints.
It is difficult to approach the ethnobotanical knowledge of all the indigenous
communities of Argentina. Many authors studied and compiled data related to the
inhabitants of different geographic regions of our territory (Scarpa 2004a, Svetaz
et al. 2010). In this chapter, we will discuss the survey information of the medicinal
plants that grows in the states of Santa Fe, Chaco and Formosa, mainly inhabited
by the original towns Tobas and Mocovíes. The phytogeographic characteristics of
the region as well as the use and properties of the medicinal plants used by these
tribes will also be presented. Finally, we will analyze statistically the main plant
families reported for medicinal purpose and the more common uses of them.
Ethnomedicinal Plants Used by Tobas and Mocovíes Tribes 189
Central region
Northeast region
Northwest region
Cuyana region
Patagonian region
Toba tribes
Mocovi tribes
Fig. 10.1. Map of different Argentinean regions showing the zones inhabited by Tobas and Mocovíes
tribes.
190 ETHNOBOTANY: Local Knowledge and Traditions
Chaquena Province
Fig. 10.2. Argentinean phytogeographic regions according to Cabrera (1976), showing Chaqueña and
the Espinal provinces where Toba and Mocoví tribes live nowadays.
Ethnomedicinal Plants Used by Tobas and Mocovíes Tribes 191
from the surroundings can be varied, in quantitative terms the animal production
destined to self-consumption and commercialization predominates widely and
has accentuated in the last decades. Tobas and Mocovíes reside in the rural area
and are mainly engaged in the extensive grazing of beef and goats cattle on fiscal
lands (Scarpa 2000).
and sprinkled with sugar, to accompany different remedies, for example, those
presented by the genus Prosopis sp. In this case, its stem embers are used
to prepare the “quemadillo” and this element accompanies many vegetable
remedies referred to as “warm” (Pen 2013).
• “Mate” has its origins in the Guaraní town and is currently consumed mostly
in southern Brazil and northern Argentina. It is a drink that is prepared using
the leaves of the “yerba mate” plant (Ilex paraguariensis), which is filtered
in hot water. Drinking mate is a very important social practice, similar to
coffee or tea. In fact, this infusion is so popular that it is the national drink
of Argentina and Paraguay. The correct preparation and consumption of the
drink is essential and specific utensils are required. The container used to
drink mate is a hollow pumpkin that is left to dry in the sun. In addition to
the pumpkin, a small bulb tube is needed, traditionally made of silver and
includes ornamental decorations although the most modern varieties can be
made of nickel or stainless steel, which are cheaper (Fig. 10.3). The mate is
prepared in the pumpkin, filling it with dried leaves of Ilex paraguariensis.
Then, a strong stir is necessary, so that the dusty residue is separated from
the leaves and hot water is poured into the pumpkin. It is important that the
water temperature oscillates between 70 and 80ºC but not boiling (Burtnik
2006, Dellacassa 2007).
• “Tereré” is a refreshing drink and also originated in the Guarani town. Its
preparation is similar to that of “mate” with the difference that “tereré”
employs water cooled with pieces of ice, and fruit juices such as orange,
grapefruit or lemon may be added (Oberti 1960).
Fig. 10.3. (A) “Yerba mate” plant (Ilex paraguariensis). (B) Hollow pumpkin and small bulb tube
used to prepare the “mate”.
Quebracho
Schinus fasciculata (Griseb.) I.M. Johnst. Molle pispito, Molle curative of cough, antidiarreheic, contraceptive, against flue stems and leaves
fragante, Molle
Apiaceae
Petroselinum crispum (Mill.) Nyman ex Perejil strengthen gums, curative of cough, contraceptive, abortive aerial parts
A.W. Hill
Pimpinella anisum L. Anís anthelmintic, against pains, abortive seeds
Apocynaceae
Asclepias mellodora A.St.-Hil Matatodo antimicrobial leaves
Aspidosperma quebracho-blanco Schltdl Quebracho blanco purgant, expectorant, against cooling and flu, antidysenteric, bark and seeds
abortive, depurative of blood, curative of cough, against
malaria, for ripen pimples, antimicrobial
Funastrum gracile (Decne.) Schltr Tramontana, Enredadera diuretic, against renal affections, antihypertensive, aerial parts
hepatic anti-inflammatory, antiperistaltic, oral antiseptic,
against Chagas disease, depurative of blood, preventive,
antidandruff, antimicrobial, vulnerary
Morrenia odorata (Hook. & Arn.) Lindl. Doca against palpitations, against bronchitis, against snake bites, Stems and flowers
antimicrobial
Vallesia glabra (Cav.) Link Ancoche, Ancochi vulnerary, for ripen pimples, against rheumatic pain, against aerial parts
cooling, childbirth stimulative
Aquifoliaceae
Ilex paraguariensis A.St.-Hil. Yerba purgant, diuretic, to cure warts, childbirth stimulative aerial parts
Asteraceae
Acanthospermum hispidum DC. Guasdrilla, Guarilla, diuretic, against malaria, febrifuge roots and branches
Guasdiya
Ambrosia tenuifolia Spreng. Altamisa, Altamisa de las anthelmintic, hepatic digestive, against sunstroke, febrifuge aerial parts
islas
Artemisia absinthium L. Ajenjo abortive, hepatic digestive, against flu and cooling leaves
Baccharis salicifolia (Ruiz & Pav.) Pers. Suncho against cooling and flu, against bones and kidneys pain, aerial parts
diuretic
Cyclolepis genistoides D.Don Palo azul diuretic, against renal affections, febrifuge, hepatic digestive, aerial parts
depurative of blood, antihypertensive
Eupatorium christieanum Baker Eupatorio against cooling and flu aerial parts
Flaveria bidentis (L.) Kuntze Balda, Balta against sunstroke branches
Parthenium hysterophorus L. Altamisa, Altamisa de anthelmintic, against rheumatic pain, against cooling and flu, aerial parts
Ethnomedicinal Plants Used by Tobas and Mocovíes Tribes
Bombacaceae
Ceiba chodatii (Hassl.) Ravenna Yuchán, Lluchán against sunstroke, curative of cough, for infected wounds, leaves and flowers
diuretic, sedative, hypocholesterolemic, against snake bites,
hepatic digestive
Borraginaceae
Borago officinalis L. Borraja, Borraja de to treat measles stems and leaves
Castilla
Heliotropium elongatum (Lehm.) Gürke Borraja e´campo, Borraja to treat measles, febrifuge, stomach digestive stems and leaves
Heliotropium procumbens Mill. Cola de gama vulnerary, antiarthritic stems and leaves
Brassicaceae
Lepidium didymum L. Quimpe, Quimpi against gingivitis, curative of cough, expectorant aerial parts
Buddlejaceae
Buddleja sp Salvia against sunstroke aerial parts
Cactaceae
Gymnocalycium mihanovichii (Fric ex against bone pains stems
Gürke) Britton & Rose
Opuntia elata Link & Otto ex Salm-Dyck febrifuge fruits
Opuntia ficus-indica (L.) Mill. against rheumatic pain, against kidney stones stems
Opuntia quimilo K. Schum. Quimil against sunstroke, diuretic, for infected wounds, febrifuge, stems
hepatic antiinflammatory, antiinflammatory, for ripen pimples
Quiabentia verticillata (Vaupel) Borg Sacha rosa for infected wounds leaves
Stetsonia coryne (Salm-Dyck) Britton et Cardón against cutaneous eruptions, hepatic digestive fruits
Rose
Capparaceae
Anisocapparis speciosa (Griseb.) Bola verde, Palo verde odontalgic, against the “cold stomach”, antidysenteric aerial parts
X. Cornejo & H.H.Iltis
Capparicordis tweedieana (Eichler) Iltis & Hoja redonda, Sacha antidisenteric, against the “cold stomach”, for ripening aerial parts
Cornejo mamita, Mataburro, pimples
Comida de burro
Capparis salicifolia Griseb. Sacha sandía diuretic fruits
Caricaceae
Carica papaya L. Mamón, Papaya anthelmintic seeds
Ethnomedicinal Plants Used by Tobas and Mocovíes Tribes
Citrullus lanatus (Thunb.) Matsum. & Sándia against measles, against general cooling fruits and seeds
Nakai
Cucumis melo L. Melón emenagogue seeds
Cucurbita maxima Duchesne Zapallo anthelmintic seeds
Cucurbita moschata Duchesne Anco against burns mucilage of the fruit
Cuscutaceae
Cuscuta indecora Choisy Cabello de ángel, Rayo antialopecic stems
de sol
Erythroxylaceae
Erythroxylum coca Lam. Coca against the “side pain”, stomach digestive, oxytocic leaves
Phyllantaceae
Phyllanthus niruri L. Rompepiedras vesicular stones, against renal affections aerial parts
Euphorbiaceae
Croton bonplandianus Baill. Escoba negra, Tinajero, hepatic digestive, antidiarreic, gastric pains aerial parts
Paloma yuyo, Comida de
paloma
Croton hieronymi Griseb. Poleo’el monte, Poleo stomach digestive aerial parts
Euphorbia serpens Kunth Yerba ’e la golondrina, stomach refreshing, oral antiseptic, hepatic digestive, against roots and aerial parts
Yerba golondrina, urinary tract irritations, diuretic, febrifuge
Golondrina
Jatropha hieronymi Kuntze; Jatropha Piñón, Manchador, for infected wounds latex
excisa Griseb. Higuera ’el monte,
Higuerilla
Manihot esculante Crantz Mandioca antidiarrheic, gut depurative, against sunstroke roots
Ricinus communis L. Tártago, Ricino against sunstroke and headache, against the “cold stomach” leaves
Sapium haematospermum Müll. Arg. Lecherón vulnerary, cicatrizant, dermic affections bark and leaves
Tragia hieronymi Pax & K. Hoffm. Yuyo quemador, against insect bites aerial parts
Quemador, Ortiguilla
Fabaceae
Acacia albicorticata Burkart Espinillo vulnerary, against throat pain bark and leaves
Cedrela sp. Cedro for the “internal blows”, against the “side pain” stems
Melia azederach L. Paraíso for cutaneous eruptions, headache, abortive, anthelmintic, leaves and roots
emenagogue
Menispermaceae
Cissampelos pareira L. Mil hombres against the “cold stomach”, depurative of blood, hepatic stems
digestive, diuretic, vulnerary, anti inflammatory, abortive
Menyanthaceae
Nymphoides indica (L.) Kuntze febrifuge leaves
Myrthaceae
Eucalyptus tereticornis Sm. Ucalito expectorant, curative of cough, against throat pain, against leaves and stems
the “air”
Nyctaginaceae
Boerhavia diffusa var. leiocarpa (Heimerl) Batata e´cuchi, Batata de stomach refreshing, diuretic, depurative of blood, febrifuge roots
202 ETHNOBOTANY: Local Knowledge and Traditions
Castela coccinea Griseb. Meloncillo, Melonciyo antidisenteric, against hypothermia, against the roots
“astonishment”
Solanaceae
Capsicum chacoense Hunz. Ají del monte, Ají stomach digestive, to wean fruits
Cestrum parqui (Lam.) L’Hér. Hediondilla against headache and sunstroke, for the “Inner fever”, roots and leaves
febrifuge, stomach refreshing, antihemorrhoidal, antipruritus
Datura ferox L. Chamico for odontological pains, vulnerary, against asthma, for ripen leaves
pimples, against headache
Nicotiana glauca Graham Palán, Palancho Anti inflammatory, against headache, for ripening pimples, leaves
febrifuge, against sunstroke, vulnerary
Nicotiana tabacum L. Tabaco against the “air”, against hypothermia leaves
Solanum aridum Morong Pocote, Pocotillo, Pocote antifungal fruits
´e perro
Solanum argentinum Bitter & Lillo Cabrayuyo general preventive, against “bone pain”, against rheumatic aerial parts
pain, against sunstroke, febrifuge, against hypothermia,
against cooling and flu, for ripen pimples
Solanum glaucophyllum Desf Corcho ´el agua, Sunho emetic aerial parts
´el agua
Solanum hieronymi Kuntze Pocote antifungal fruits
Solanum sisymbrifolium Lam. Vila vila intestinal refreshing, hepatic digestive, febrifuge, oral roots
antiseptic, diuretic, against irritation of the urinary tract,
depurative of blood, curative of cough, general preventive,
contraceptive
Solanum tuberosum L. Papa Anti inflammatory tubers
Theaceae
Camellia sinensis (L.) Kuntze Té for ophthalmic infections leaves
Urticaceae
Parietaria debilis G. Forst. Paletaria against irritation of the urinary tract, hepatic and intestinal aerial parts
refreshing, febrifuge
Verbenaceae
Aloysia gratissima (Gillies & Hook.) Tronc. Poleo del campo digestive, carminative, tonic, against palpitations, nervous leaves
diseases, antifungal
Aloysia polystachya (Griseb.) Moldenke Burrito, Poleo, Poleo de la stomach and hepatic digestive, hypertensive, against aerial parts
casa, Cedrón palpitations, for nervous diseases
Glandularia tweedieana (Niven ex Hook.) Margarita, Sangre de febrifuge, for ripen pimples, emenagogue aerial parts
Ethnomedicinal Plants Used by Tobas and Mocovíes Tribes
P. Peralta Cristo
Table 10.1 contd. …
205
…Table 10.1 contd.
Species Vernacular name Medicinal uses Utilized parts
Lantana trifolia L. Salvia ´e monte stomach digestive leaves
Lippia alba (Mill.) N.E.Br. ex Britton & Salvia de castilla, Salvia against cooling and flu, against throat pain, against gastric aerial parts
P.Wilson de la casa, Salvia pains and headache, curative of cough
Phyla reptans (Kunth) Greene Mosko yuyo, Mosko yuyo for infected wounds and gangrene, against skin rashes, aerial parts
del bajo against sunstroke
Viscaceae
Phoradendron liga (Gillies ex. Hook. & Liga, Corpo oxytocic, antihypertensive, against hypothermia aerial parts
Arn.) Eichler; Phoradendron bathyoryctum
Eichler
Vitaceae
Cissus palmata Poir Zarzaparrilla, Zarza, blood depurative, hepatic refreshing leaves
Enredadera, Bejuco´el
agua
Zygophylaceae
Bulnesia sarmientoi Lorentz ex Griseb. Palo santo hepatic digestive, against the “internal blows” and the “side aerial parts
pain”, febrifuge, blood depurative, against hypothermia,
206 ETHNOBOTANY: Local Knowledge and Traditions
Typha dominguensis Pers. Totora diuretic, purgant, antidisenteric, anti-allergic rhizomes and leaves
207
208 ETHNOBOTANY: Local Knowledge and Traditions
are sorted according to the same criteria, by their scientific name including their
vernacular names, medicinal applications and used parts. All the data related to the
uses are briefly presented, since all the information is much broader and is related
to the respective cultural context (Crovetto 1968, Marzocca 1997, Lahitte 1998,
Hurrell 2011, Scarpa 2013).
From the information summarized in Table 10.1, it can be observed that plant
families most used by these communities belong to dicotyledonous class (90%),
while monocots are scarcely used for medicinal purposes, representing only 10% of
the total species reported in this work. Within dicotyledons, the most prominent used
families are: Fabaceae (11%), Asteraceae (9%), Solanaceae (8%), Euphorbiaceae
(6%), Cactaceae (4%), Verbenaceae (4%), Amaranthaceae (4%), Apocynaceae (4%),
Cucurbitaceae (3%), Lamiaceae (3%), Borraginaceae (2%), Capparaceae (2%),
Malvaceae (2%), Rutaceae (2%), Anacardiaceae (2%) and another 34 families that
each one constitutes 1% of the total dicotyledons surveyed (Fig. 10.4).
Regarding the most important medicinal uses of the 156 plants surveyed, they
were grouped into 17 different categories. It should be noted that the description of
the uses of plants by the inhabitants of these communities is much more detailed
and descriptive, but this grouping into categories was carried out in order to shorten
the information and draw some broad conclusions about the use of their plants. It
is important to mention that a plant species can be used for one or several ailments
categories.
The percentages of plants used for the different categories are the following
(Fig. 10.5): odontalgic disease (10%), ophthalmic disease (4%), antiparasitic
(17%), antiinflammatory (4%), kidney dysfunctions (21%), female health problems,
childbirth & abortive (21%), digestive tract ailments (45%), antimicrobials
(11%), febrifuge (24%), respiratory disease (20%), depurative and purgant (15%),
rheumatic and general pains (12%), sunstroke (10%), anti-hypertensive and heart
problem (12%), headache (5%), skin diseases and wounds (35%), others (21%).
100% 40%
90%
90% 35%
80%
30%
70%
25%
60%
20%
50%
15%
40%
10%
30%
5%
20%
10% 0%
e e e e e e e e e e e e e e
10% ea a ea ae ea ea ea ea ea ea ea ea ea ea ea
rs
ac iace ac ace ac tac rac tac iac bac iac vac tac nac nac
e
th
h c a i l
nt n r i n b m u
R ola rbe
O
d b a a
0% r a rca ocy ste rag Ca app rcu hor F La M S
a a p A or C u
C Eu
p Ve
Monocotyledon Dicotyledon Am An A B
50%
45%
40%
35%
30%
25%
20%
15%
10%
5%
0%
c
e
nt
ge
iti
ns
em
e
ts
ke
s
ns
e
e
ls
as
tiv
y
nd
as
as
ch
as
en
or
ifu
ia
ai
s
tro
io
rg
or
se
bl
er
se
ar
ou
b
lp
da
se
at
ct
lm
br
pu
ab
ro
ns
ro
di
tip
th
un
di
ra
w
di
ea
Fe
ai
tp
ic
Su
c
&
&
An
ne
O
ic
sf
&
ry
tim
gi
H
ct
ar
fla
e
rth
lm
dy
al
to
ge
e
tra
iv
he
An
in
as
nt
ta
ra
bi
at
ey
ti-
&
e
do
ph
ild
pi
&
se
ur
tiv
An
dn
ic
es
e
ep
O
ch
O
di
es
at
iv
Ki
in
ns
um
s,
ig
Sk
m
rte
he
le
pe
ob
hy
pr
ti-
th
An
al
he
e
al
m
Fe
Fig. 10.5. Percentages of medicinal plants used by Tobas and Mocovíes for different ailments
categories.
A B C D
E F G
Fig. 10.6. Pictures of the seven most important medicinal species of this Argentinean region: (A)
Schinus molle, (B) Salix humboldtiana, (C) Gomphrena tormentosa, (D) Commelina erecta, (E)
Clematis montevidiensis, (F) Cestrum parqui, (G) Baccharis salicifolia.
Conclusion
Native peoples of Argentina represent a very important cultural value for the
country. Thermal and climatic amplitudes of the region offer a biodiversity of
plants that constitutes an amazing natural resource. Two of the main communities
that inhabit the “Chaqueña” and the “Espinal” phytogeographic provinces are
the Tobas and Mocovíes tribes. Ethnobotanical data look upon a wide range of
information regarding the ways in which these cultural communities interact
with its plant environment and the knowledge associated to a plant species. It
was possible to compile the ethnobotanical information of 156 vegetal species
existing in different texts and specialized reports, concluding that the main families
used by these tribes are: Fabaceae, Asteraceae, Solanaceae, Euphorbiaceae,
Cactaceae, Verbenaceae, Amaranthaceae, Apocynaceae, Cucurbitaceae, Lamiaceae,
Borraginaceae, Capparaceae, Malvaceae, Rutaceae and Anacardiaceae. The most
important medicinal uses of the 156 plants surveyed correspond to the categories
of: odontalgic disease, ophthalmic disease, antiparasitic, anti-inflammatory, kidney
dysfunctions, female health problems, digestive tract ailments, antimicrobials,
febrifuge, respiratory disease, depurative and purgant, rheumatic and general pains,
sunstroke, anti-hypertensive and heart problem, headache and skin diseases and
wounds. The forms of the remedies’ preparation using medicinal plants is quite
212 ETHNOBOTANY: Local Knowledge and Traditions
varied and these tribes use three particular ways such as “quemadillo”, “mate”
and “tereré”. Finally, we can conclude that most important medicinal species
of this Argentinean region are: Schinus molle, Salix humboldtiana, Gomphrena
tormentosa, Commelina erecta, Clematis montevidiensis, Cestrum parqui and
Baccharis salicifolia, among others.
References
Adámoli, J., Neumann, R., Ratier de Colina, A. and Morello, J. 1972. El Chaco aluvional salteño.
Revista de Investigaciones Agropecuarias 9: 165–238.
Arenas, P. 1987. La etnobotánica en el Gran Chaco. VI Congreso Latinoamericano de Botánica, Simposio
de Etnobotánica, Serie Memorias de Eventos Científicos Colombianos, Medellín ICFES, 35–42.
Ávila, M. 1960. Flora y Fauna en el folklore de Santiago del Estero, Ed. M. Violetto, San Miguel de
Tucumán, p. 254.
Bates, D. 1985. Plant utilization: Patterns and prospects. Economic Botany 39: 241–265.
Berry, P.E. 2002. Diversidad y endemismo en los bosques neotropicales de bajura. pp. 83–96. In:
Guariguata, M. and Catan, G. (eds.). Ecología y Conservación de Bosques. Libro Universitario
Regional (Eulac/GTZ), Cartago.
Brandão, M., Zanetti, N., Oliveira, P., Grael, C., Santos, A. and Monte-Mór, R. 2008. Brazilian medicinal
plants described by 19th century European naturalists in the Official Pharmacopoeia. Journal of
Ethnopharmacology 120: 141–148.
Burtnik, O. 2006. Yerba Mate: Manual de Producción. INTA, AER Santo Tomé, Corrientes, Argentina,
p. 52.
Cabrera, A. 1971. Fitogeografía de la República Argentina. Boletín de la Sociedad Argentina de
Botánica 14: 1–42.
Cabrera, A. 1976. Enciclopedia Argentina de Agricultura y Jardinería: Regiones Fitogeográficas
Argentinas. Acme.
Cabrera, A. and Willink, A. 1980. Biogeografía de América Latina. Monografía 13. Serie de Biología,
Secretaría General de la Organización de los Estados Americanos, Washington DC, EEUU, p. 120.
Carrizo, J. 1960. Algunas supersticiones medicinales del Norte argentino. Cuadernos del Instituto
Nacional de Investigaciones Folklóricas 1: 160–175.
Cleaves, C. 2001. Etnobotánica médica participativa en el Parque Nacional Lachua (Thesis). Universidad
de San Carlos de Guatemala, Guatemala.
Coelho de Souza, G., Haas, A., von Poser, G., Schapoval, E. and Elisabetsky, E. 2004.
Ethnopharmacological studies of antimicrobial remedies in the south of Brazil. Journal of
Ethnopharmacology 90: 135–143.
Correia, P. 1984. Dicionário de Plantas Úteis do Brasil e Das Exóticas Cultivadas. Instituto Brasileiro
de Desenvolvimiento Forestal, Imprenta Nacional, Río de janeiro, p. 490.
Crovetto, R.M. 1968. Introducción a la Etnobotánica aborigen del nordeste argentino. Etnobiológica
11: 1–10.
Cruz, M., Santos, P., Barbosa Jr., A., de Mélo, D., Alviano, C., Antoniolli, A., Alviano, D. and Trindade,
R. 2007. Antifungal activity of Brazilian medicinal plants involved in popular treatments of
mycoses. Journal of Ethnopharmacology 111: 409–412.
Daoud, D. 1954. Veterinaria y medicina popular en Tucumán. Boletín de la Asociación Tucumana de
Folklore 6(3): 30–87.
Dellacassa, E., Cesio, V., Vázquez, A., Echeverry, S., Soule, S., Ferreira, F. and Heinzen, H. 2007.
Yerba mate. Historia, uso y propiedades. Revista de la Asociación de Química y Farmacia del
Uruguay 51: 16–20.
Di Lullo, O. 1929. La medicina popular de Santiago del Estero, Ed. El Liberal, Santiago del Estero, p. 171.
Di Lullo, O. 1946. Contribución al estudio de las voces santiagueñas. Ed. Gobierno de la Provincia de
Santiago del Estero, Santiago del Estero, p. 371.
Ethnomedicinal Plants Used by Tobas and Mocovíes Tribes 213
Estévez, Y., Castillo, D., Tangoa Pisango, M., Arévalo, J., Rojas, R., Alban, J., Deharo, E., Bourdy,
G. and Sauvain, M. 2007. Evaluation of the leishmanicidal activity of plants used by Peruvian
Chayahuita ethnic group. Journal of Ethnopharmacology 114: 254–259.
Goleniowski, M., Bongiovanni, G., Palacio, L., Núñez, C. and Cantero, J. 2006. Medicinal plants
from the “Sierra de Comechingones”, Argentina. Journal of Ethnopharmacology 107: 324–341.
Grornbridge, E. 1992. Global diversity Status of the Earth’s Living Resources.
Gupta, M. 1995. 270 Plantas Medicinales Latinoamericanas, CYTED-SECAB, Bogotá, p. 617.
Gupta, M. 2008. Plantas medicinales Iberoamericanas, Convenio Andrés Bello Ed., Bogotá, p. 520.
Hurrell, J., Ulibarri, E., Arenas, P. and Pochettino, M. 2011. Plantas de herboristería, Ed. LOLA, Buenos
Aires, Argentina, p. 242.
Lahitte, H., Hurrell, J., Belgrano, J., Jankowski, M., Haloua, L. and Mehltreter, M. 1998. Plantas
medicinales rioplatenses: plantas nativas y naturalizadas utilizadas en medicina popular en la
región del Delta del Paraná, Isla Martín García y Ribera Platense. Ed. LOLA, Buenos Aires,
República Argentina, p. 240.
Martin, G. 1995. Ethnobotany. Chapman & Hall, London, p. 268.
Marzocca, A., Fernández, M. and Fernández, A. 1997. Vademécum de malezas medicinales de la
Argentina: indígenas y exóticas. Orientación Gráfica, Buenos Aires, Argentina, p. 352.
Morton, J. 1981. Atlas of medicinal plants of Middle America: Bahamas to Yucatan. Charles C. Thomas.
Murillo, A. 1889. Plantes médicinales du Chili. Exposition Universelle de Paris, section chilienne,
Lagny, París.
Oberti, F. 1960. Disquisiciones sobre el origen de la bombilla. Cuadernos del Instituto Nacional de
Antropología y Pensamiento Latinoamericano 1: 151–158.
Pen, C., Romero, C., Deza, M., Durando, P. and Barioglio, C. 2013. Las Prácticas Culturales de
Pequeñas Productoras Caprinas de los Departamentos Cruz del Eje e Ischilín de la Provincia de
Córdoba, Argentina. VII Jornadas Santiago Wallace de Investigación en Antropología Social.
Sección de Antropología Social. Instituto de Ciencias Antropológicas. Facultad de Filosofía y
Letras, UBA, p. 11.
Portillo, A., Vila, R., Freixa, B., Adzet, T. and Cañigueral, S. 2001. Antifungal activity of Paraguayan
plants used in traditional medicine. Journal of Ethnopharmacology 76: 93–98.
Rosenblat, A. 1954. La población indígena y el mestizaje en América: La población indígena, 1492–1950.
Instituto de Filología de la Universidad de Buenos Aires, Biblioteca Americanista, Ed. Nova, p. 79.
Scarpa, G. 2000. Plants employed in traditional veterinary medicine by the Criollos of the Northwestern
Argentine Chaco. Darwiniana 38: 253–265.
Scarpa, G. 2004a. Medicinal plants used by the criollos of northwestern Argentine Chaco. Journal of
Ethnopharmacology 91: 115–135.
Scarpa, G. 2004b. El síndrome cálido-fresco en la medicina popular criolla del Chaco argentino. Revista
de Dialectología y Tradiciones Populares 59(2): 5–29.
Scarpa, G. 2013. Las plantas en la vida de los criollos del oeste formoseño: medicina, ganadería,
alimentación y viviendas tradicionales. Ed. Rumbo Sur Asociación Civil, Buenos Aires, República
Argentina, p. 237.
Sosa Verón, H. and Vivante, A. 1951. Algunas recetas supersticiosas de Río Hondo (Santiago del
Estero). Revista del Instituto de Antropología de la Universidad Nacional de Tucumán 5: 89–102.
Sturzenegger, O. 1987. Medecine traditionnelle et pluralisme medical dans une culture creole du Chaco
Argentin. Mémoire pour le D.E.A. Anthropologie: Biologie Humaine et Société, Universite de
Droit, D’Economie et des Sciences D’Aix-Marseille, France, p. 72.
Sturzenegger, O. 1989. Maladie et environnement culturel: à propos des “Culture-bond syndromes”.
Ecologie Humaine 7: 53–62.
Sturzenegger, O. 1999. Le mauvais oeil de la lune: Ethnomédecine créole en Amérique du Sud. Ed.
Karthala, Paris, p. 302.
Svetaz, L., Zuljan, F., Derita, M., Petenatti, E., Tamayo, G., Cáceres, A., Cechinel Filho, V., Giménez,
A., Pinzón, R., Zacchino, S. and Gupta, M. 2010. Value of the ethnomedical information for the
discovery of plants with antifungal properties. A survey among seven Latin American countries.
Journal of Ethnopharmacology 127(1): 137–158.
Torres, M. 1975. Ingeniero Guillermo Nicasio Juárez y los parajes del oeste de Formosa, Tiempo de
hoy, Buenos Aires, p. 167.
CHAPTER 11
Introduction
At the dawn of 20th century, fresh plants were more widely used for medicinal
purposes. Increased investments into cultivation of medicinal plants and their more
organised and effective usage have marked the decades of the century and opened
novel paths in the study of plants and its potentially beneficial properties. Despite
many advantages of modern medicine, traditional medical treatment is of great
importance. Medicinal plants are widely applied in traditional medicine and have
been an irreplaceable aspect of cultural heritage of diverse nations, both in the past
and the present. The knowledge of beneficial active substances of plants has lately
influenced the global increase in the medicinal application of various herbs. Their
popularity may have been due to their status of inexpensive raw materials which
contain products with increased biological activity particularly useful in prevention
of various metabolism disorders (Petrovska 2012).
Medicinal plants are applied either independently or in combination with
synthetic drugs. The efficiency of phytotherapy largely depends on the active
components identified in the herbs used as well as on the appropriately established
diagnosis and dose. Previous extensive studies and technological developments
have contributed to the recognition of significance medicinal plants have in
medicine and pharmacy. Plant origin preparatus has become widely applicable in
various domains. Pharmacies all over the world sell teas, extracts or pills made
of medicinal plants. Plant products in the medicines show multilevel biological
activity and therefore have diuretic, sedative, antiseptic, antioxidant, antidiabetic
Department of Biology and Ecology, Faculty of Science, University of Kragujevac, Radoja Domanovića
12, 34000 Kragujevac, Republic of Serbia.
* Corresponding author: [email protected]
Ethnobotany of Teucrium Species 215
Botanical Common Names Part Used Therapeutic Use Manipulation Biological Activity Notes
Name
Teucrium Wall germander, Aerial parts Skin inflammations, Infusion, decoction, Antioxidant, Large doses
chamaedrys L. podubica, dubačac strengthening of the immune tincture, elixirs, antiproliferative, cause liver
system, anaemia powder antiinflammatory, damage
antimicrobial and
antiseptic
Teucrium Mountain germander, Aerial parts Respiratory inflammations, Infusion, powder, Antioxidant, antiviral, Used in
montanum L. trava iva, dubačac Strengthening of the immune tincture antimicrobial, aromatising
mali system, stress, tiredness, anticancer, wines, liquers,
stimulation of bile secretion, antispasmodic and and rakija
stimulation of digestion, loss of antipyretic Leaves are used
appetite, cleaning wounds to flavour meat
Teucrium Felty germander, Aerial parts Inflammations, diabetes, Infusion, powder Antioxidant, Large doses
polium L. kalpooreh, pepeljuša rheumatism, indigestion, antidiabetic, cause liver
abdominal pain, headache, antiinflammatory, damage
kidney rocks antispasmodic,
antipyretic,
216 ETHNOBOTANY: Local Knowledge and Traditions
antimicrobial,
antifungal and antiviral
Teucrium Croatian germander, Aerial parts Scarce data Infusion Antioxidant, No data
arduini L. planinska metvica antimicrobial and
antiviral
Teucrium botrys Cut leaf germander, Aerial parts Strengthening of the immune Infusion Antioxidant, No data
L. dubačac crveni system, cold, enhancing antimicrobial and
digestion, kidney diseases anticancer
Teucrium Water germander, Aerial parts Infectious skin diseases, Infusion Antioxidant, No data
scordium subsp. vodeni dubačac diseases of digestive tract, antiproliferative and
scordium increased temperature and fever, antifungal
respiratory disorders, poisoning,
a cough, intestinal parasites
Teucrium Water germander, Aerial parts Respiratory disorders Infusion Antioxidant, No data
scordium subsp. lukovac antimicrobial,
scordioides anticancer and
proapoptotic
Teucrium Tree germander, Aerial parts Diuretic and depurative effects Infusion Antioxidant and No data
fruticans L. žbunasti dubačac antimicrobial
Teucrium Yellow germander, Aerial parts Diabetes, external treatment Infusion Antiinflammatory, No data
flavum L. žuti dubačac of skin traumas, cleaning of antidiabetic, anticancer,
wounds antioxidant and
antimicrobial
Ethnobotany of Teucrium Species
217
218 ETHNOBOTANY: Local Knowledge and Traditions
of the genus Teucrium are distributed in both southern parts of the continent and
certain nearby islands (Fig. 11.1) (Meusel et al. 1978, Hollis and Brummitt 1992).
Out of the total number of 250 species of the genus Teucrium, approximately
200 species are found in the Mediterranean area. The widest distribution has been
recorded on the Iberian peninsula whereas the smallest distribution has been
observed on the Apennine peninsula. The areas of Northern Africa, Asia Minor
and the Balkans are registered as having a significant number and wide variety of
species. About ten species of the genus are found in Australia and America.
In terms of distribution, it is necessary to emphasise that there is a small
number of widely distributed species, i.e., there are more moderately distributed or
even endemic species. Teucrium chamaedrys, Teucrium montanum and Teucrium
scordium are among the most frequently found species on the territory of Europe
(Tutin and Wood 1972, Diklić 1974, Meusel et al. 1978).
The species of the genus Teucrium grow on all types of calcareous soil.
However, seldom are these plants found on serpentine and silicate substrates. Saline
soils are also regarded as unfavourable for the species in question. These species
may be found in mountain, hill and lowland localities such as arid, termophilous
habitats with high level of insolation. A small number of the species grows in
humid lowland areas. Deciduous, mixed, and coniferous forests, communities of
herbaceous vegetation, rocky habitats, meadows, pastures, continental steppes and
sands have been confirmed as established habitats of the species. Ocassionally, the
species may grow in hygrophilous communities along rivers as well as in ruderal
habitats (Horvat et al. 1974, Diklić 1974, Ellenberg and Strutt 2009).
1 2 3
5 6 7 9
Fig. 11.2. Described Teucrium species: (1) T. chamaedrys; (2) T. montanum; (3) T. polium; (4)
T. arduini; (5) T. botrys; (6) T. scordium subsp. scordium; (7) T. scordium subsp. scordioides; (8)
T. flavum; (9) T. fruticans.
220 ETHNOBOTANY: Local Knowledge and Traditions
short petiole and dentate margins. Flowers are located in the basis of bracts. The
calyx has mild dorsal protuberance and is covered in hairs. Mildly red corolla is
twice or thrice as long as calyx. Stamens, located above flowers, are slightly bent.
Fruits are ovoid nuts (Stanković et al. 2010, Stanković 2012a).
Teucrium chamaedrys is a Mediterranean and Middle European species
distributed in whole Europe, save for the northern part of the continent. It can also
be found in northern Africa and western Asia (Horvat et al. 1974, Diklić 1974,
Stanković 2012а).
The species Teucrium chamaedrys mostly grows in arid rocky localities of
calcareous origin. Rarely can it be found on serpentine and silicate substrate. The
species may inhabit areas whose altitudes range from 200 to 1500 m (Horvat et al.
1974, Diklić 1974). It is widely distributed in deciduous, mixed, and coniferous
forests as well as in communities of broadleaved evergreen and deciduous forests
of bushy vegetation. Meadows, pastures, continental steppes and sands are also
frequent habitats of Teucrium chamaedrys (Horvat et al. 1974, Diklić 1974,
Ellenberg and Strutt 2009).
Teucrium chamaedrys is used for preparing teas, tinctures, wines and other
therapeutic products which havе bitter taste due to the presence of bitter active
substances. These substances positively influence digestive system and may be used
in the treatment of skin inflammation and anaemia as well as for the purpose of
strengthening the immune system. The species is used as an ingredient of different
elixirs, rakijas made with different medicinal herbs, and traditional drink vermouth.
The tea is made out of dried herb and water. It is taken before meal 2 or 3 times
a day. The tincture is made of dried herb and rakija. After 8 days, the mixture is
filtered and 30 drops of the filtered content is used before every meal. Tincture
powder is used to strengthen the organism in quantities of 5 to 10 g a day (Sarić
1988, Kojić et al. 1998, Keršek 2006, Stanković et al. 2012b).
Germander is widely applied as food supplement either in combination with
other herbs or as capsules available in 200 mg dose (Barceloux 2012). Long term
usage of the species Teucrium chamaedrys may cause liver damage as it contains
secondary metabolites from the group of neo-clerodane diterpenes such as Teucrin
А (Savvidou et al. 2007). On average, 100 ml of germander tea contains between
75 and 150 mg of Tеucrin А (Barceloux 2012). Consequently, the usage of teas and
other products made of this species must be moderate and carefully dosed (Khleifat
2002). US FDA has allowed metabolite Teucrin A as flavouring agent in alcoholic
drinks such as aromatic wines, vermouth or bitter drinks (Barceloux 2012).
When it comes to phenolic content of the above ground parts of the species
Teucrium chamaedrys, quantitative and qualitative analyses of flavonoids have
shown high concentrations of luteoline and apigenin. Among other detected
substances are phenylpropanoid glicosides, diterpenes and phenolic acids. The most
important glicosides are teucroside, verbascoside, teucroside-3-O-methyl ether
and teucroside-3,4-O-dimethyl ether. Among detected diterpenes are Teucrin A,
Teucrin G, teuflin and dihydroteugin. With regard to phenolic acids, the presence
of caffeine and rosemary acid has been confirmed (Gafner et al. 2003, Avula et al.
Ethnobotany of Teucrium Species 221
2003, Bosisio et al. 2004, Bruno et al. 2004, Kadifkova-Panovska et al. 2005, Lin
et al. 2009). By the examination of quantity and content of evaporable components
using GC/MC analysis, it has been established that the principal components of
essential oil are β-caryophyllene and germacrene D (Bežić et al. 2011).
By following the influence of neo-clerodane diterpenes isolated from the
species Teucrium chamaedrys on seed germination and growth and development of
young plants of the species Dactylis hispanica Roth, Petrorhagia velutina (Guss.)
Ball et Heyw., Phleum subulatum (Savi) Asch. et Gr., the allelopathic effect of
secondary metabolites of the species has been observed (Fiorentino et al. 2009).
The extracts of the species Teucrium chamaedrys have antioxidant (Kadifkova-
Panovska et al. 2005), proapoptotic (Stanković et al. 2011a), genotoxic,
antimutagenic (Milošević-Djorđević et al. 2013), antiinflammatory (Pourmotabbed
et al. 2010), antimalarial (Tagarelli et al. 2010), antimicrobial and antiseptic (Vlase
et al. 2014) activity in both in vitro and in vivo conditions. Apart from the previously
stated effects, it has been established that Teucrium chamaedrys has a significant
cytotoxic impact on HCT-116 cells after 24 hour exposure (Stanković et al. 2011a).
The previously conducted analysis showed that the species from serpentine
habitats are important in terms of biological activity as it contains greater
concentrations of phenols and flavonoids and shows high level of antioxidant
activity. Therefore, Teucrium chamaedrys from these habitats is safe for use as it
does not contain heavy metals (Zlatić et al. 2017).
Teucrium montanum L.
Teucrium montanum (Fig. 11.2.2) is a perennial plant with developed semi-woody
root. The well spread branches either rise or cover the ground and may reach the
length between 5 and 25 cm. The leaves are oppositely arranged, lanceolate, with
entire margins, narrowed in the upper parts. Abaxial side is covered in white hair,
whereas adaxial side may be hairless. The flowers form dichasium and their stalks
are short. Corolla is of pale yellow colour. Stamens, reaching over corolla, are
located between upper corolla lobes. The fruits are nuts of ovoid shape (Stanković
et al. 2011b, Stanković 2012a).
Teucrium montanum grows in southern Europe as well as in southern parts
of Western and Eastern Europe, Asia Minor and in northern Africa. It is widely
distributed in Mediterranean areas as mountain species (Horvat et al. 1974, Diklić
1974, Stanković 2012a).
The habitats of Teucrium montanum are calcareous rocks, pine forests on
calcareous soil, pastures and occasionally serpentine substrate. The species may
inhabit areas whose altitudes range from 30 to 2000 m (Horvat et al. 1974, Diklić
1974, Stanković 2012a).
It grows in mixed, coniferous and deciduous forests, in serpentine rocky
habitats, gorges and canyons as well as in the communities in sub-Mediterranean
region, xerophytic and mountainous habitats (Horvat et al. 1974, Diklić 1974,
Ellenberg and Strutt 2009).
222 ETHNOBOTANY: Local Knowledge and Traditions
For centuries, peoples of the Balkans have kept to traditional belief that this
herb is medicinal and highly beneficial. Teucrium montanum is used in the treatment
of inflammations of respiratory system and to strengthten the organism in stressful,
tiring and physically demanding conditions. Teas, tinctures and wines stimulate
bile secretion, suppress a cold, relieve digestive problems and enhance digestion.
When it comes to gallbladder disorders, a tincture is used. Tincture is made of
20 g of dried herb and 100 ml of rakija. After 14 days, the compound is macerated
and filtrated. The maximum amount to be taken is 20 drops per dose dissolved in
water or tea of some other herb thrice a day. Tea is prepared in standard manner
and daily intake is limited to less than 3 cups. The powder of plant may be used
for similar purposes and the maximum amount of it is 1 to 3 g per dose thrice a
day before meal (Sarić 1988, Kojić et al. 1998). Teucrium montanum is mixed with
other herbs for purpose of making different elixirs and medicinal types of rakija
(Keršek 2006). The species is widely used as a natural medicine for diseases related
to disorders of bile secretion, liver and lack of appettite. As for external application,
it is predominantly used for treating and cleaning wounds and other skin traumas.
HPLC analysis of phenols of the species Teucrium montanum confirmed that
genistein acid is the predominant phenolic acid. Though quantitatively present to
a lesser degree, it is important to bring up a variety of other detected acids such as
chlorogenic, coumarin, syringic, gallic, vanillin, caffeine and ferulic acid (Tumbas
et al. 2004, Čanadanović-Brunet et al. 2006). Quantitative analysis of etheric
oil by means of GC/MC test showed that the main components are: β-cadinene,
β-selinene, α-calacorene, β-caryophyllene, β-pinene and germacrene (Vuković et
al. 2008, Bežić et al. 2011).
The extracts of the species Teucrium montanum have antioxidant (Čanadanović-
Brunet et al. 2006), antiviral (Bežić et al. 2011), antimicrobial (Stanković et al.
2012b), genotoxic, antimutagenic (Milošević-Djorđević et al. 2013), antirheumatic,
antispasmodic and antipyretic activity (Shah and Shah 2015). In terms of anticancer
effect, Teucrium montanum extracts have shown a significant level of cytotoxic
activity on HeLa and K562 cancer cell lines (Stanković et al. 2015).
The up to date research showed that Teucrium montanum from serpentine
localities show high level of biological activity reflected in the total content of
phenols and flavonoids as well as in intense antioxidant effect. Consequently, due
to the undetected presence of heavy metals, Teucrium montanum from serpentine
habitats is safe for wide application (Zlatić et al. 2017).
Teucrium polium L.
Teucrium polium (Fig. 11.2.3) is a perennial plant with semi-bushy above ground
plant parts and well developed semi-woody root. The branches are upright,
moderately developed and may grow up to 40 cm. Sessile hairy leaves are
oppositely arranged, elongated, slightly oval and dentate at the top. The flowers
Ethnobotany of Teucrium Species 223
are zygomorphic and form dichasium. The whole surface of calyx is covered in
white hair. Corolla leaves are mostly white in colour. Upper labia make two oval
oppositely arranged lobes. The length of anthers rarely surpasses the length of
corolla. The fruits are ovoid nuts (Stanković 2012a).
The species Teucrium polium is distributed in southern Europe, northern Africa
and Asia Minor. It inhabits localities at an altitude varying from 300 m to 1000
m. It grows mostly on arid and rocky terrains, in gorges and canyons as well as
in sub-Mediterranean regions and xerophile communities (Tutin and Wood 1972,
Horvat et al. 1974, Diklić 1974, Ellenberg and Strutt 2009, Stanković 2012a).
Teucrium polium is used in traditional medicine in the treatment of different
physiological disorders such as inflammation, diabetes, rheumatism or diseases of
gastrointestinal tract. The tea of the species is used to enhance digestion, to alleviate
abdominal pain, to mitigate the symptoms of the most serious type of diabetes as
well as in the treatment of cold, a headache, kidney stones and excessive sweating
(Afifi et al. 2009, Vahidi et al. 2010, Jaradat 2015).
Quantitative and qualitative analyses of secondary metabolites in watery and
alcoholic extract have shown that flavonoids apigenin and luteolin are the most
frequently found secondary metabolites in the above ground plant parts of Teucrium
polium (Safaei and Haghi 2004). Among other important and often detected active
substances are rutin, cirsiliol, diosmetin, cirsimaritin and cirsilineol (Kadifkova
Panovska et al. 2005, Sharififar et al. 2009, Stefkov et al. 2011). Examination of
etheric oil from above ground plant parts demonstrated that the principal evaporable
components of the species Teucrium polium are germacrene, linalool, ρ- cimen,
carvon, β-caryophyllene, α-pinene, β-pinene, carvacrol and caryophyllene oxide
(Afifi et al. 2009, Moghtader 2009, Menichini et al. 2009, Bežić et al. 2011).
The previous studies have shown that the extracts of Teucrium polium
have antioxidant, antidiabetic, antiinflammatory, antispasmodic, antipyretic,
antimicrobial, antifungal and antiviral activity (Jaradat 2015). When it comes to
antioxidant effects of the species, the previously conducted research has shown
that Teucrium polium extracts may be regarded either as equally or even more
efficient than Ginkgo and Green tea extracts (Stanković et al. 2012c). As for the
anticancer effect of Teucrium polium, metabolites from the extract of the species
may be used in the treatment of prostate cancer as these inhibit signaling pathway
which leads to metastasis of cancer (Kanduoza et al. 2010). In treating cell cultures
of glioblastoma, alveolar adenocarcinoma, breast cancer and adrenal gland with
extracts of the species Teucrium polium, it has been established that secondary
metabolites of the plant show significant cytotoxic activity in in vitro conditions
(Eskandary et al. 2007, Nematollahi-Machani et al. 2007). Analysis of the impact of
water extract of Teucrium polium on NSCLS cell line of lung cancer demonstrated
that the extract shows intense antiproliferative activity by inhibiting cell cycle and
causing death of cell (Haidara et al. 2011). Ethanol extract of the species Teucrium
polium enhances the effect of vincristine, vinblastine and doxorubicin which are
widely used in cancer treatment (Rajabalijan 2008).
224 ETHNOBOTANY: Local Knowledge and Traditions
Teucrium arduini L.
Teucrium arduini (Fig. 11.2.4) is a perennial plant with moderately branched hairy
and woody older shoots which may grow up to 50 cm in height. The leaves are oval,
petiolated, with well developed leaf nervature, serrated margins and extended base.
Flowers are densely arranged into clusters that look like raceme inflorescence. They
open up from the basis up to the top of spike. Calyx is differentiated into upper
and lower labia. Hairy corolla is mostly white in colour and its size surpasses the
size of calyx. Stamens grow beyond corolla and have reddish anthers. The fruit is
ovoid nut (Stanković 2012a).
Teucrium arduini is an endemic species native to the Balkan Peninsula, that
is, it grows on the territory encompassing the belt from northwestern Albania to
northwestern Croatia (Kremer et al. 2011).
Teucrium arduini grows on calcareous substrate. It inhabits arid, termophile
rocky habitats located at an altitude varying between 50 and 1500 m. Calcareous
rocks, cliffs, canyons and gorges of mountain regions are also well known types
of habitat of the species (Tutin and Wood 1972, Horvat et al. 1974, Diklić 1974,
Ellenberg and Strutt 2009, Stanković 2012a).
There is scarcity of data on quantitative and qualitative content of secondary
metabolites of the species Teucrium arduini. Examination of the quantity and content
of evaporable components in the above-ground plant parts of the species Teucrium
arduini by means of GC/FID and GC/MS tests demonstrated that predominant
components of etheric oil are β-caryophyllene, caryophyllene oxide and germacrene
D. As for flavonoids, the presence of cirsimarin, characteristic of this species of
the genus Teucrium, has been confirmed (Vuković et al. 2011, Dunkić et al. 2011).
The extracts of the species Teucrium arduini show high level of antimicrobial,
antiviral and antioxidant activity (Šamec et al. 2010, Stanković et al. 2012b, Kremer
et al. 2013). The most prominent proapoptotic effect of Teucrium arduini on HCT-
116 cells was observed after a three-day long exposure (Stanković et al. 2011a).
Teucrium botrys L.
Teucrium botrys (Fig. 11.2.5) is an annual, rarely biannual herbaceous plant.
The semi-woody root is well branched. The hairy shoots are upright, moderately
branched, greenish or red in colour and may grow up to 40 cm in height. The
oppositely arranged, hairy leaves are cut into 5 to 7 lobes with well developed stalk.
Zygomorphic flowers are vertically set in comparison with the stem. They form
dense clusters shorter than bracts. Tube-like, hairy calyx has dorsal protuberance
of tubular part. Corolla is purple with dark streaks. Its external surface is hairy.
Stamens and style of gynoecium are longer than corolla. Dark nut fruits are circular
or ovoid in shape (Stanković 2012a).
Teucrium botrys is distributed in Middle Europe and in northwestern Africa.
It grows on calcareous substrate and inhabits open, arid and rocky areas, formerly
cultivated soil, rocky pastures, arid places beside roads and generally, localities at
Ethnobotany of Teucrium Species 225
up to 1.500 m of altitude (Tutin and Wood 1972, Horvat et al. 1974, Diklić 1974,
Ellenberg and Strutt 2009, Stanković 2012a).
This species, as all others which belong to the genus Teucrium, has medicinal
properties. It is used to strengthen the immune system, to relieve symptoms of cold,
in the treatment of kidney diseases and to enhance digestion (Stanković 2012a).
There is little data on the results of research on quantitative and qualitative
characteristics of secondary metabolites of the species Teucrium botrys. Analyses
of chemical composition of essential oil obtained from the above ground plant
parts of the species have shown the presence of significant concentrations of neo-
clerodane diterpenoids 19-deacetylteuscorodol and teubotrin as well as of diterpenes
such as teucvidin, montanine D, teuchamedryn С and 6β-hydroxyteusoordin.
19-deacetylteuscorodol and teubotrin are significant for the species Teucrium botrys
in chemotaxonomic terms (De La Torre et al. 1986).
Biological activity of extracts of the species Teucrium botrys is reflected in its
antioxidant, antimicrobial and anticancer activity (Stanković et al. 2012b, Fajfarić
2013). With regard to antioxidant efficiency, Teucrium botrys extracts are proved
to be either equally or even more efficient than Ginkgo and Green tea extracts
(Stanković et al. 2014). When it comes to anticancer effects, Teucrium botrys
extracts have shown a significant level of cytotoxic activity on HeLa and K562
cancer cell lines (Stanković et al. 2015).
Teucrium flavum L.
Teucrium flavum L. (Fig. 11.2.8) is a perennial, evergreen, bushy species with shoots
reaching up to 60 cm. The stem is upright, hairy and branchy, with ovoid, mildly
dentate leaves and small flowers of pale yellow colour. The species mostly inhabits
xerophyll, calcareous and rocky areas located at up to 1000 m of altitude. It can
Ethnobotany of Teucrium Species 227
Teucrium fruticans L.
Teucrium fruticans L. (Fig. 11.2.9) is a perennial, evergreen, bushy species
with shoots reaching up to 2 m. The above ground plant part is branchy. The
oval leaves of grey-green colour on adaxial side and grey-white on abaxial side
have a thick indumentum. Blue flowers are quite small. The species grows in
termophile calcareous habitats in western Mediterranean region. In other parts
of the Mediterranean, the species is successfully cultivated (Frabetti et al. 2009,
Stanković and Zlatić 2017).
Teucrium fruticans L. is appreciated to a great extent in central parts of Italy
due to its pharmacological properties. The leaf of the species is used to prepare
nfusion with diuretic and depurative effects. The extracts of this species contain
neo-clerodane diterpenes germacrene D and β-caryophyllene. High amounts of
β-pinene and β-myrcene as well as flavonoid compounds cirsilineol and cirsimaritin
which show high level of biological activity were also detected (Kisiel et al. 2001,
Frabetti et al. 2009, Acquaviva et al. 2017). The extracts of the species from Spain
have antimicrobial and antioxidant effect and may be used in food, pharmaceutical
and cosmetic industry (Stanković et al. 2017).
Conclusions
Last decades have brought new tendencies in the treatment of numerous disorders
and diseases. The supremacy of pharmacological industry has been challenged
by traditional medicine. Plant species have significant place in contemporary folk
medicine. This chapter is a review of morphological, chemical and medicinal
properties, of geographical distribution as well as of ethnobotanical and commercial
application of 9 selected species of the genus Teucrium. The studies conducted so
far have proved and confirmed the presence of metabolites and other beneficial
228 ETHNOBOTANY: Local Knowledge and Traditions
References
Acquaviva, R., Genovese, C., Amodeo, A., Tomasello, B., Malfa, G., Sorrenti, V., Tempera, G., Addamo,
A.P., Ragusa, S., Rosa, T., Menichini, F. and Giacomo, C.D. 2017. Biological activities of Teucrium
flavum L., Teucrium fruticans L., and Teucrium siculum rafin crude extracts. Plant Biosyst. http://
dx.doi.org/10.1080/11263504.2017.1330773.
Afifi, F.U., Abu-Irmaileh, B.E. and Al-Noubani, R.A. 2009. Comparative analysis of the esential oils
of Teucrium polium L. grown in different arid & semi-arid habitats in Jordan. Jordan J. Pharm.
Sci. 2: 42–52.
Avula, R., Manyam, R.B., Bedir, E. and Khan, I.A. 2003. Rapid separation and determination of
four phenylpropanoid glycosides from T. chamaedrys by capillary electrophoresis method.
Chromatographia 8: 751–755.
Barceloux, D.G. 2012. Medicinal toxicology of natural substances. Foods, fungi, Medicinal herbs,
plants and venomous animal. John Wiley & Sons, Hoboken.
Bedir, E., Manyam, R. and Khan, I.A. 2003. Neo-clerodane diterpenoids and phenylethanoid glycosides
from Teucrium chamaedrys L. Phytochemistry 63: 977–983.
Bezić, N., Vuko, E., Dunkić, V., Ruščić, M., Blažević, I. and Burčul, F. 2011. Antiphytoviral activity of
sesquiterpene-rich essential oils from four Croatian Teucrium species. Molecules 16: 8119–8129.
Bosisio, E., Giavarini, F., Dell’Agli, M., Galli, G. and Galli, C.L. 2004. Analysis by high-performance
liquid chromatography of teucrin A in beverages flavoured with an extract of Teucrium chamaedrys
L. Food Addit. Contam. 21: 407–414.
Bruno, M., Piozzi, F., Rosselli, S., Maggio, A., Alania, M., Lamara, K., Al-Hillo, Y.R.M. and Servettaz,
O. 2004. Phytochemical investigation of four Teucrium species. Rev. Soc. Quím. Mex. 48: 137–138.
Čanadanović-Brunet, J., Djilas, M.S., Ćetković, S.G., Tumbas, T.V., Mandić, I.A. and Čanadanović,
M.V. 2006. Antioxidant activities of different Teucrium montanum L. extracts. Int. J. Food Sci.
Tech. 41: 667–673.
De La Torre, C.M., Fernández-Gadea, F., Michavila, A., Rodríguez, B., Piozzia, F. and Savonaa, G.
1986. Neo-clerodane diterpenoids from Teucrium botrys. Phytochemistry 25: 2385–2387.
Diklić, N. 1974. Teucrium L. pp. 349–356. In: Josifović, M. (ed.). Flora of Federative Republic of
Serbia, Belgrade.
Dunkić, V., Bezić, N. and Vuko, E. 2011. Antiphytoviral activity of essential oil from endemic species
Teucrium arduini. Nat. Prod. Commun. 9: 1385–1388.
Ellenberg, H. and Strutt, K.G. 2009. Vegetation Ecology of Central Europe, 4th ed., Cambridge
University Press.
Eskandary, H., Rajabalian, S., Yazdi, T., Eskandari, M., Fatehi, K. and Ganjooei, A.N. 2007. Evaluation
of cytotoxic effect of Teucrium polium on a new glioblastoma multiforme cell line (REYF-1)
using MTT and soft agar clonogenic assays. Int. J. Pharmacol. 3: 435–437.
Fajfarić, M. 2013. Antioxidant activity of the plant species Teucrium botrys L. Dissertation. Faculty of
Pharmacy and Biochemisty. University of Zagreb. Croatia.
Fiorentino, A., D’Abrosca, B., Esposito, A., Izzo, A., Pascarella, M.T., D’Angelo, G. and Monaco,
P. 2009. Potential allelopathic effect of neo-clerodane diterpenes from Teucrium chamaedrys
(L.) on stenomediterranean and weed cosmopolitan specieс. Biochem. Syst. Ecol. 37: 349–353.
Frabetti, M., Gutiérrez-Pesce, P., Mendoza, D.E., Gyves, E. and Rudini, E. 2009. Micropropagation of
Teucrium fruticans L., an ornamental and medicinal plant. In vitro Cell. Dev. Biol. 45: 129–134.
Gafner, S., Bergeron, C., Batcha, L.L. and Angerhofer, C.K. 2003. Analysis of Scutellaria lateriflora
and its adulterants Teucrium canadense and Teucrium chamaedrys by LC-UV/MS, TLC, and
digital photomicroscopy. J. AOAC Int. 86: 453–460.
Ethnobotany of Teucrium Species 229
Milošević-Đorđević, O., Stošić, I., Stanković, M. and Grujičić, D. 2013. Comparative study of
genotoxicity and antimutagenicity of methanolic extracts from Teucrium chamaedrys and Teucrium
montanum in human lymphocytes using micronucelus assay. Cytotechnology 65: 863–869.
Monsef-Esfahani, R.H., Miri, A., Amini, M., Amanzadeh, Y., Hadjiakhoondi, A., Hajiaghaee, R. and
Ajani, Y. 2010. Seasonal variation in the chemical composition, antioxidant activity and total
phenolic content of Teucrium persicum Boiss. essential oils. Res. J. Biol. Sci. 5: 492–498.
Moghtader, M. 2009. Chemical composition of the essential oil of Teucrium polium L. from Iran. Am.
Eurasian J. Agric. Environ. Sci. 5: 843–846.
Morteza-Semnani, K., Saeedi, M. and Akbarzadeh, M. 2007. Essential oil composition of Teucrium
scordium L. Acta Pharmacol. 57: 499–504.
Nematollahi-Mahani, S.N., Rezazadeh-Kermani, M., Mehrabani, M. and Nakhaee, N. 2007. Cytotoxic
Effects of Teucrium polium on some established cell lines. Pharm. Biol. 45: 295–298.
Petrović, S. 1883. Medicinal plants of Serbia, Serbian archive for medicine, Belgrade.
Petrovska, B.B. 2012. Historical review of medicinal plants usage. Pharmacogn. Rev. 6: 1–5.
Piozzi, F., Bruno, M., Rosselli, S. and Maggio, A. 2005. Advances on the chemistry of furano-diterpenoids
from Teucrium genus. Heterocycles 65: 1221–1234.
Pourmotabbed, A., Farshchi, A., Ghiasi, G. and Khatabi, M.P. 2010. Analgesic and anti-inflammatory
activity of Teucrium chamaedrys leaves aqueous extract in male rats. Iran. J. Basic Med. Sci.
13: 119–125.
Rajabalian, S. 2008. Methanolic extract of Teucrium polium L. potentiates the cytotoxic and apoptotic
effects of anticancer drugs of vincristine, vinblastine and doxorubicin against a panel of cancerous
cell lines. Exp. Oncol. 30: 133–138.
Redžić, S.S. 2007. The ecological aspect of ethnobotany and ethnopharmacology of population in
Bosnia and Herzegovina. Coll. Antropol. 31: 869–890.
Safaei, A. and Haghi, G. 2004. Identification and quantitative determination of flavonoids in the aerial
parts of Teucrium polium by HPLC. Int. J. Pharm. Res. 3: 90.
Sarić, R.M. 1988. Medicinal plants of Federative Republic of Serbia, Serbian Academy of Sciences
and Arts, Belgrade, pp. 640.
Savvidou, S., Goulis, J., Giavazis, I., Patsiaoura, K., Hytiroglou, P. and Arvanitakis, C. 2007. Herb-
induced hepatitis by Teucrium polium L.: report of two cases and review of the literature. Eur. J.
Gastroenterol. Hepatol. 19: 507–511.
Šamec, D., Gruzb, J., Strnadb, M., Kremerc, D., Kosalecc, I., Grubešić, J.R., Karlović, K., Lucica, A.
and Piljac-Žegaraca, J. 2010. Antioxidant and antimicrobial properties of Teucrium arduini L.
(Lamiaceae) flower and leaf infusions (Teucrium arduini L. antioxidant capacity). Food Chem.
Toxicol. 48: 113–119.
Sharififar, F., Dehghn-Nudeh, G. and Mirtajaldini, M. 2009. Major flavonoids with antioxidant activity
from Teucrium polium L. Food Chem. 112: 885–888.
Shah, M.M.S. and Shah, H.M.S. 2015. Phytochemical, antioxidant, antinociceptive and anti-
inflammatory potential of the aqueous extracts of Teucrium stockisianum bioss. BCM Complement.
Altern. Med. 15: 351.
Stanković, M.S., Topuzović, M., Solujić, S. and Mihailović, V. 2010. Antioxidant activity and
concentration of phenols and flavonoids in the whole plant and plant parts of Teucrium chamaedrys
L. var. glanduliferum Haussk. J. Med. Plants Res. 4: 2092–2098.
Stanković, M.S., Ćurčić, M.G., Žižić, J.B., Topuzović, M.D., Solujić, S.R. and Marković, S.D. 2011a.
Teucrium plant species as natural sources of novel anticancer compounds: Antiproliferative,
Proapoptotic and Antioxidant Properties. Int. J. Mol. Sci. 12: 4190–4205.
Stanković, M.S., Nićiforović, N., Topuzović, M. and Solujić, S. 2011b. Total phenolic content,
flavonoid concentrations and antioxidant activity, of the whole plant and plant parts extracts
from Teucrium montanum L. var. montanum, f. supinum (L.) Reichenb. Biotechnol. Biotechnol.
Equip. 25: 2222–2227.
Stanković, M.S. 2012a. Biological Effects of Secondary Metabolites of the Species of the genus
Teucrium L. of Serbian flora. Dissertation. Faculty of Science. University of Kragujevac. Serbia.
Ethnobotany of Teucrium Species 231
Stanković, M.S., Stefanović, O., Čomić, Lj., Topuzović, M., Radojević, I. and Solujić, S. 2012b.
Antimicrobial activity, total phenolic content and flavonoid concentrations of Teucrium species.
Cent. Eur. J. Biol. 7: 664–671.
Stanković, M.S., Nicifirović, N., Mihajlović, V., Topuzović, M. and Solujić, S. 2012c. Antioxidant
activity, total phenolic content and flavonoid concentrations of different plant parts of Teucrium
polium L. subsp. polium. Acta Soc. Bot. Pol. 81: 117–122.
Stanković, M.S., Jakovljević, D., Topuzović, M. and Zlatković, B. 2014. Antioxidant activity and
content of phenolics and flavonoids in the whole plant and plant parts of Teucrium botrys L.
Oxid. Commun. 37: 522–532.
Stanković, M.S., Mitrović, T.Lj., Matić, I.Z., Topuzović, M.D. and Stamenković, S.M. 2015. New
values of Teucrium species: in vitro study of cytotoxic activities of secondary metabolites. Not.
Bot. Horti. Agrobo. 43: 41–46.
Stanković, M.S., Stojanović-Radić, Z., Blanco-Salas, J., Vázquez-Pardo, F.M. and Ruiz-Téllez, T.
2017. Screening of selected species from Spanish flora as a source of bioactive substances. Ind.
Crops Prod. 95: 493–501.
Stanković, M. and Zlatić, N. 2017. The total quantity of phenolic compounds and antioxidant activity
of the selected specie of the genus Teucrium. XXII Counselling on Biotechnology, Faculty of
Agronomy Čačak, University of Kragujevac, Serbia, pp. 515–520.
Stefkov, G., Kulevanova, S., Miova, B., Dinevska-Kjovkarovska, S., Møjgaard, P., Jäger, A.K. and
Josefsen, K. 2011. Effects of Teucrium polium spp. capitatum flavonoids on the lipid and
carbohydrate metabolism in rats. Pharm. Biol. 49: 885–892.
Sundaresan, P.R., Slavoff, S.A., Grundel, E., White, K.D., Mazzola, E., Koblenz, D. and Rader, L. 2006.
Isolation and characterisation of selected germander diterpenoids from authenticated Teucrium
chamaedrys and T. canadense by HPLC, HPLC-MS and NMR. Phytochem. Anal. 17: 243–250.
Tagarelli, G., Tagarelli, A. and Piro, A. 2010. Folk medicine used to heal malaria in Calabria (Southern
Italy). J. Ethnobiol. Ethnomed. 6: 27.
Tumbas, T.V., Mandić, I.A., Ćetković, S.G., Djilas, M.S. and Čanadanović-Brunet, M.J. 2004. HPLC
analysis of phenolic acids in Mountain Germander (Teucrium montanum L.) extracts. Acta
Periodica Technologica 35: 265–273.
Tutin, T.G. and Wood, D. 1972. Teucrium. pp. 129–135. In: Tutin, T.G., Heywood, V.H., Burges, N.A.,
Moore, D., Valentine, D. and Walters, S. (eds.). Flora Europaea, 1st Ed. Cambridge University
Press, Cambridge, England.
Vahidi, A.R., Dashti-Rahmatabadi, M.H. and Bagheri, S.M. 2010. The effects of Tecrium polium boiled
extract in diabetic rats. Int. J. Diabetes Obes. 2: 27–31.
Vlase, L., Benedec, D., Hanganu, D., Damian, G., Csillaq, I., Sevastre, B., Mot, A.C., Silaghi-Dumitrescu,
R. and Tilea, I. 2014. Evaluation of antioxidant and antimicrobial activities and phenolic profile
for Hyssopus officinalis, Ocimum basilicum and Teucrium chamaedrys. Molecules 19: 5490–5507.
Vuković, N., Milošević, T., Sukdolak, S. and Solujić, S. 2008. The chemical composition of the essential
oil and the antibacterial activities of the essential oil and methanol extract of Teucrium montanum.
J. Serb. Chem. Soc. 73: 299–305.
Vukovic, N., Sukdolak, S., Solujic, S., Mihailovic, V., Mladenovic, M., Stojanovic, J. and Stankovic,
M.S. 2011. Chemical composition and antimicrobial activity of Teucrium arduini essential oil
and cirsimarin from Montenegro. J. Med. Plants Res. 5: 1244–1250.
Zlatić, N.M., Stanković, M.S. and Simić, Z.S. 2017. Secondary metabolites and metal content dynamics
in Teucrium montanum L. and Teucrium chamaedrys L. from habitats with serpentine and
calcareous substrate. Environ. Monit. Assess. 189: 110.
CHAPTER 12
Ethnobotanical Issues on
Medicinal Plants from Paraguay
Rosa Luisa Degen de Arrúa,1,* Yenny González1 and
Esteban A. Ferro B.2
Introduction
Paraguay is a land-locked country located in the sub-tropical region of South
America. It has a area of 406,760 km2, distributed in two big regions separated
by Paraguay river. The country does not have any relevant heights, but it is gifted
with a rich flora with about 5,500 to 6,000 vascular species. Among those, a
considerable amount has medicinal uses in the country (Mereles 2014). This use
of plants can be traced back to the oldest cultural traditions, and medicinal plants
were established as the base of traditional medicine (Bertoni 1927), practices that
are still present today. The recognition of these plants’ value comprises their use
for health preservation and treatment, becoming valuable sources of raw material
for the extraction of bioactive molecules to be employed alone or following either
chemical or microbial processing, and even more, providing lead structures for
the development of new molecules directed to treat a variety of diseases (Ibarrola
and Degen 2011).
The plants employed for medicinal purposes receive several names, such
as diet supplements, traditional medicine or phytotherapeutic remedies, and the
WHO supports the implementation of these therapeutic resources among the state
members. The utilization of medicinal plants evokes different reactions among
1
National University of Asunción, Faculty of Chemical Sciences, Research Department, Department
of Botany, Paraguay.
2
National University of Asunción, Faculty of Chemical Sciences, Research Department, Department
of Phytochemistry, Paraguay.
* Corresponding author: [email protected], [email protected]
Ethnobotanical Issues on Medicinal Plants from Paraguay 233
different societies, going from the enthusiasm without any criticism to the extreme
lack of credibility. Yet, their use as alternative and complement treatments is quickly
increasing in developed countries; however, in developing countries, these resources
remain widely applied, strongly enough to be the first therapeutic resource in
several countries. This is a frequent practice in Latin American countries, including
Paraguay. Some countries of the region have established legal frameworks and
standardized criteria in order to fulfill safety, effectiveness and quality requirements
for herbal remedies, in order to make reliable products available for the population,
reducing these risks associated with the consumption of plant-derived medicines
(Ibarrola and Degen 2011). It is considered as a priority for the country to have a
national policy for medicinal plants and phytotherapeutic resources. Such policy
would help to guarantee the safe and rational use of those products as valuable
resources for primary health care by rural and urban populations (Degen et al. 2009).
The aim of this chapter is to review the background of the use of medicinal
plants in Paraguay, their conservation and trading conditions, the advance in research
efforts and their future perpectives.
Fig. 12.1. Ilex paraguariensis var. paraguariensis, “yerba mate”, medicinal plant.
(Photo: Germán González, Department of Botany).
uses. By 1877, Domingo Parodi prepared a list of plants using both Spanish and
Guarani names, specifying botanical families and names, and their medical use.
More recently, Moses Bertoni a naturalist from Switzerland, studied the Paraguayan
flora. He settled in Paraguay by the end of 19th century and described the most used
plants in Paraguay and the neighboring countries, in alphabetical order. Moreover,
he recovered information from the aboriginals, and by the end of 1899 discovered
the species recognized as ‘sweet herb’ or ka’á he’ẽ (Fig. 12.2), Stevia rebaudiana
(González Torres 1992, MAG-DGPE 2008, Scavone 2010). Between centuries 19th
and 20th, two botanists made great collections of the flora from Paraguay. They
were the Swiss Dr. Emil Hassler, and the Paraguayan Teodoro Rojas, considered
as the first botanist from Paraguay, since the previous botanists came from other
countries. Teodoro Rojas worked hardly under the influence of great botanists,
like the previously mentioned E. Hassler and M. Bertoni, among others. Rojas
became an expert technician in systematic botany, collecting thousands of species,
describing new ones and publishing several works (Basualdo 1993). His collections,
performed in Paraguay, Bolivia and Argentina reached 12,837 records, during his
50 years of activity as a botanist collecting about 40,000 samples, counting both
original samples and duplicates (Schinini 2005).
More recently, Prof. Dionisio González Torres published in 1970 the first
edition of his book entitled “Catálogo de plantas medicinales y alimenticias y
útiles usadas en el Paraguay” (Catalogue of medicinal, edible and useful plants
employed in Paraguay). In this book, he presented 1,500 popular names of
plants, alphabetically ordered, their scientific names, properties and attributes,
and preparation procedures. Most of the named species were autochthonous, but
exotic species were also included, following a vast review of the bibliography,
with information collected by naturalists from centuries 16th to 19th, as a result
of interviews performed in different areas of the country along several years. This
book was considered as the only one with enough records on medicinal plants from
Paraguay for a long time, and even at the present time it is considered as a valuable
starting point to perform research and academic works.
Another outstanding researcher of Paraguayan natural environment is Dr.
Carlos Gatti Battilana, who expanded his interests in social problems, focusing his
attention on both Guarani civilization and the Paraguayan population of the 20th
century. Such interest resulted in the publication of a Spanish–Guarani dictionary
for medical use, where is recorded an important content of the medical Guarani
knowledge, obtained from his patients (Benítez 1986). At this point, we must
name pharmacist Rómulo Feliciángeli, who prepared in 1939 the project of the
Paraguayan Pharmacopoeia. This work included an addendum, containing 33 plant
species used at that time for medicinal purposes (Feliciángeli 1939).
In 1978, Prof. Isabel Basualdo and her all female research team from the
Facultad de Química y Farmacia (Chemistry and Pharmacy School), today Facultad
de Ciencias Químicas, FCQ (Chemical Sciences School), started their research
works for the recovery of the popular knowledge on the use of medicinal plants in
Paraguay, backed by the botanical identification of the species and the preservation
of voucher specimens. This activity made possible to set up the Herbarium of the
Chemical Sciences School of the Universidad Nacional de Asunción, which is
internationally recognized as FCQ for its acronym in Spanish.
Between 1982 and 1985, the United Nations Development Program supported
the training of human resources and provided basic equipment required to start
chemical studies on medicinal plants from Paraguay. As a result of this project,
chemical studies on species from Asteraceae and Celastraceae families were
executed. Following these efforts, a joint project between the FCQ and the Medical
and Pharmaceutical University of Toyama, Japan—with the support of the Japan
International Cooperation Agency (JICA)—was executed with two main objectives:
to record with documentary backing the medicinal flora from Paraguay, and to
236 ETHNOBOTANY: Local Knowledge and Traditions
evaluate its biological activity in a bioassay panel. These works allowed to publish
in 1987 a document summarizing both chemical and pharmacological findings
from herbs collected in Paraguay. A few years later, following the same research
line, a list of medicinal plants commercialized in popular markets in Asunción and
its metropolitan area was published (Basualdo et al. 2004), and more recently the
Illustrated catalogue with 80 medicinal plants from Paraguay was also published.
This work was awarded with the National Science Award, granted by the National
Congress of Paraguay to the researchers from FCQ in 2012 (Degen and González
2014b).
Several researchers have published lists of medicinal plants that include their
popular and scientific names, and also their descriptions, applications, preparation
mode and habitat, all backed by herbarium reference material. These names are
usually related to some location, village or native community, as observed in the
ethnobotanical works published by Pastor Arenas and Ricardo Moreno Azorero
(1976, 1977). They started their research with a project on the genetic characteristics
of indigenous populations, focusing initially on the Maká community characterized
by its high level of isolation and the preservation of their language and manners.
Later, they followed their studies in other native communities such as Nivakle,
Ayoreo and others, getting relevant results. In Maká community, they found high
inbreeding, high mortality and low fertility rates, which moved them to study how
the natives controlled the fertility to find medicinal plants as natural resources for
birth control. A total of 22 plant species were recorded as abortive, contraceptive,
sterilizing and fecundating from ten different ethnic groups and native communities
from Paraguay.
After that, Mereles and Degen (1994a, 1997) published a list containing 31
trees and bushes from 16 botanical families, growing in the Boreal Chaco region
and employed by native populations. Basualdo et al. (1977) described useful plants
growing at Cerro Corá National Park, at Amambay Department in the Northeastern
region of Paraguay. Mereles (2001) mentioned the useful plants from Tebicuary-
mí and Capiibary basin of Paraguay Eastern region, just to name other studies in
the subject.
Different authors have published books on medicinal plants and related issues.
We can mention Soria and Basualdo (2005), who recorded plants employed in a
community from Caazapá, Pin et al. (2009) who presented a list of medicinal plants
cultivated at the Asunción Botanical Garden, and other authors as Vera (2009, 2011),
Ibarrola and Degen (2011), Scavone (2011), who described traditional application
of medicinal plants in popular environment. Polini et al. (2013) published two
books containing the description of traditional use of medicinal plants by the Enxet
community, located in the western region of Paraguay. The later authors performed
studies that allowed rescuing the traditional knowledge about medicinal plants,
its distribution, conservation status, pharmacological properties and chemical
composition, among other data. Finally, it should be mentioned that the two editions
of the book about medicinal plants from Latin America, edited by Gupta (1995,
2008) include plants used as medicine in Paraguay.
Ethnobotanical Issues on Medicinal Plants from Paraguay 237
The Ministry of Health and Social Welfare (MSPyBS) from Paraguay started
in 2008 a process directed to include the traditional medical practices as a relevant
component of the primary health services (APS) in order to make health services
accessible to the communities. Within this concept, Soria and Ramos (2015)
published a guide of medicinal plants aimed to ease the recognition of these
species by the primary health practitioners in APS units, linking the traditional
knowledge with the formal health services. Following this initiative, Maidana et al.
(2015) have named the plant species employed by type 2 diabetes mellitus patients
receiving attention within the framework of the Diabetes National Program from
the Paraguayan Ministry for Health and Wellbeing.
Fig. 12.4. Cyclolepis genistoides, “palo azul” (blue stick) and “matorro negro” (black bush).
(Photo: Giuseppe Polini, Intercultural Pharmacies Project).
“climbing liana”, with several examples as ysypo he’é “sweet liana” (Rynchosia
senna), ysypo hú “black liana” (Adenocalymma marginatum) and ysypo kamby
“milky liana” (Morrhenia odorata). Trying to identify those species cultivated as
menta (peppermint) and menta’i (peperina) in Paraguay, a project was performed
where two species were recognized, Mentha arvensis and M. spicata, two hybrids
Ethnobotanical Issues on Medicinal Plants from Paraguay 239
markets in different cities (Fig. 12.6). The people trading in such stands, known as
“yuyeros” o “yuyeras” (herb sellers), are also recognized as key informants about
the use of plants. Following this methodology, Basualdo and Soria (1996a) reported
20 species of aromatic plants employed for medicinal use, including whole plants
and plant organs like roots, leaves, rhizomes, aerial parts and flowering tops. In
the same year, these authors published a report on 24 species employed to treat
respiratory tract diseases (Basualdo and Soria 1996b). As a continuous effort in
the same way, Basualdo et al. (2004) published a list containing 266 plant species
regularly commercialized in popular markets from Asuncion metropolitan area.
This list included plants from 82 botanical families, with 85 medical indications
for different plant organs. The list also included plants employed for preparing
refreshing beverages, as Gomphrena decumbens and Euphorbia serpens, among
others. Pin et al. (2009) recorded 510 medicinal species in the markets of Asunción,
San Lorenzo and Luque, belonging to 94 botanical families; 309 out of those
species were included in the book Plantas Medicinales del Jardín Botánico de
Asunción (Medicinal Plants from Asuncion Botanical Garden), which contains
the basic description in order to identify them. Degen and González (2014a),
retrieving information through regular visits to the main markets from Asunción,
San Lorenzo, Luque and Caacupé, reported 37 different species and one variety
among those was employed as anti-inflammatory; they belonged to 27 botanical
families, and included species like Verbena litoralis, Sida cordifolia and Schinus
weinmannifolius.
Discrepancies in the use of medicinal plants were reported when different
communities or country regions were surveyed, as mentioned by Mereles (2001),
who reported 51 species with their applications, among those growing in the basins
of rivers Tebicuary-mí and Capiibary, comprising the departments of Guairá,
Caazapá, Paraguarí and a little area from Caaguazú department. These locations
have experienced heavy deforestation resulting in the disappearance of some
Fig. 12.6. Medicinal plant from Paraguay commercialized in popular markets from Asuncion.
(Photo: Yenny González, Department of Botany).
Ethnobotanical Issues on Medicinal Plants from Paraguay 241
species, and the concomitant loss of the knowledge about their use. It is relevant
to mention that among such species, two ferns were scarcely mentioned previously
as medicinal like Microgramma vaccinifolia (Polypodiaceae) and Lycopodiella
cernua, (Lycopodiaceae).
Another relevant contribution was provided by Soria and Basualdo (2005),
who mentioned 55 species employed in a rural community from Caazapa
departament. They recorded plant species collected in the surroundings, including
modified soils, such as Chenopodium ambrosioides, Solanum sisymbrifolium, and
Senna occidentalis, while other species were obtained from the wild forests, like
Allophylus edulis (Fig. 12.7), Macfadyena unguis-catis, Sorocea bonplandii, and
Eugenia uniflora. Besides those, other species were grown in gardens and orchards,
like avocado (Persea Americana), wormwood (Artemisia absinthium), anise
(Pimpinela anisum), rye (Hordeum vulgare), lemongrass (Cymbopogon citratus)
and Plectranthus barbatus.
Vera (2009) reported 60 species, comprising both autochthonous and exotic
plants among those employed in the buffering zone of the three protected wild
areas, belonging to the private natural reserve “Tapytá”, located within San Rafael
and Caazapá National Parks.
In a recent survey performed in the communities Itá Azul (Fig. 12.8) and
San Gervasio, located in a protected area of Ybyturuzu, Guaira department, the
inhabitants mentioned 68 medicinal plant species, distributed in 35 botanical
families. Most of the named plants belong to the following families: Asteraceae,
Rutaceae, Fabaceae, and Lamiaceae. The named medical conditions related to these
species were grouped into 11 categories, the digestive and respiratory ailments being
the most frequently mentioned. In this study, a quite unusual report was observed:
2 species of Orquidaceae family, Aspidogyne kuczynskii and Miltonia flavescens,
Fig. 12.8. Itá Azul Community located in a protected area of Ybyturuzú, Guairá Department.
(Photo: Germán González, Department of Botany).
were mentioned in this area as medicinal, probably collected in the wild (Degen
and González 2014b).
González et al. (2013) reported a list comprising 15 medicinal species belonging
to 15 different botanical families from a survey performed at Pikysyry, Cordillera
department (Fig. 12.9). The ailments for which these species are employed are
diverse: four species were reported to treat respiratory conditions, three for digestive
problems, two for lowering cholesterol, two as hypotensive, two for liver diseases,
and one species for diabetes, diarrhea, cancer, heart ailments, wound cleaning,
herpes wounds and appendicitis, respectively. Leaves and aerial parts were the
parts most frequently employed.
Mereles (2006) mentioned the use of medicinal plants thriving in wetlands
areas as a current practice in Paraguay. One of the species growing in slow-flowing
surface waters is Victoria cruziana, of which leaves are used to prepare infusions to
treat respiratory tract diseases. Soria et al. (2006) had recorded 25 medicinal species
that grow in wetlands, damped and exposed to flood soils, swamps and flooded
channels. The conservation of these species is at risk due to dramatic modification
of soils, mainly related to the road building and rice plantations.
Concerning those plants growing in the Paraguayan Western region or Chaco,
Mereles and Degen (1994a, 1997) quoted 29 plant species from 16 botanical families
popularly employed for medicinal purposes, as referred by native communities,
rural inhabitants, and even some immigrants living in the surrounding of Mennonite
settlements in Central Chaco. Recently, a research study performed on the Enxet
community from that region identified 165 medicinal species referred by shamans,
chieftains, native leaders, elderly people of both sexes, men and women. Thirty
one out of these species are exclusively employed by shamans to treat ailments,
and 19 plants are used for the reproductive function in women (Polini et al. 2013).
Vera (2011) quoted 30 plant species employed to prepare phytomedicines,
presented as syrups, ointments or capsules. Among many others, it is common
to find Aloe vera, Cecropia pachystachya, Cymbopogon citratus, Eucalyptus sp.,
Piper regnellii and Rosmarinus oficinalis.
To describe a view beyond the informal trading of medicinal plants, Degen
et al. (2004) named 108 different species that are currently commercialized by
local enterprises comprising activities like distribution, fractioning and packaging
of medicinal and aromatic plants, either as powders or coarsely crushed dry
plant material; among such species could be mentioned “koku”, Allophyllus
edulis, Scoparia dulcis, Stevia rebaudiana, Menta x piperita, Maytenus ilicifolia
(Fig. 12.10), and Cecropia pachystachya.
It is remarkable to name one of the foremost published works about the
consumption of medicinal plants by patients. In the present case, Maidana et al.
(2015) reported that 78.1% out of 61 type-2 diabetes mellitus patients used medicinal
plants; 33 species from 25 botanical families were identified, mostly consumed
along with prescription drugs. The most frequently species named in that work are
Moringa oleífera, Artemisia absinthium, Tithonia diversifolia, Baccharis trimera
and Stevia rebaudiana. Besides this, Soria and Ramos (2015) named 23 plant species
that, based on scientific evidence, could be useful in primary health care; mostly
employed for this purpose are Menta x piperita, Artemisia absinthium, Eugenia
uniflora, Lippia alba and Allophylus edulis. The authors also cited some species
considered harmful to humans.
A landmark concerning the use of medicinal plants by humans in Paraguay
was the controlled clinical trial reported by Achucarro et al. (2011), describing the
effect of tablets prepared with Stevia rebaudiana leaf powder on intestinal parasites.
244 ETHNOBOTANY: Local Knowledge and Traditions
like rue, Ruta chalepensis; for wound washing like Acanthospermum australe; as
poultices with chamomile, Matricaria chamomilla, or to prepare hot baths with
bitter orange leaves, Citrus aurantium, respectively (Basualdo et al. 2003, Degen
and González 2014a). More recently, the consumption of processed composite
yerba mate, Ilex paraguariensis—a mixture of yerba mate with other plants—and
the “flavored composite yerba mate” which contains one or more essential oils,
became popular. Peppermint, boldo, and lemon are the herbs and flavors most
frequently added (Degen et al. 2011).
Even at the present time, it is quite usual to find in Asuncion downtown
and other Paraguay main cities medicinal plant sellers in street stalls, who also
recommend different medicinal plants to the clients, according to their ailments
or requirements. These plants are offered fresh, usually comprising mixtures of
two or more species, crushed in a mortar and packed in a plastic bag, ready to be
mixed with water for “tereré”. It is remarkable that the clients of such stalls are
either young or elder people, from different social status, which affirms that “tereré”
consumption is a deeply rooted tradition in the Paraguayan population. Along with
the promotion of processed yerba mate and other plant-related products through
mass media, younger generations are acquiring the practice of “tereré” consumption
which is also a relevant way for medicinal plants use. In such a way, two popular
practices like the consumption of both the traditional beverage “tereré” and the
medicinal plants are being consolidated as a part of Paraguayan traditions in the
whole society, instead of being lost over the years (Degen and González 2014a).
packing enterprises also trade medicinal plants as crushed material or dried powders.
Besides this, processing industries for both food products and phytomedicines
prepare syrups, ointments and capsules based on medicinal plants.
From the 108 medicinal species named by Degen et al. (2004), 66% were
native, 9% imported and 25% cultivated; out of the 41 cultivated species, 13 were
native and 27 acclimatized. The species with the highest demand were Allophyllus
edulis, Scoparia dulcis, Stevia rebaudiana, Menta x piperita, Maytenus ilicifolia,
Cecropia pachystachya, Cassia angustifolia and Peumus boldus. Some of the
species showed high demand, with seasonal variations; chamomile (Matricaria
chamomilla), and flaxseed (Linum usitatissimun), were sold throughout the whole
year; however, others like borage (Borago officinalis) were just demanded in the
cold weather season. The use of some species has also followed fashion tendencies
like Macfadiena unguis-cati, or Uncaria sp. and Moringa oleifera, just to mention
a few (Degen et al. 2004, Degen and González 2014a).
The medicinal plants business usually gets raw material from collectors who
buy the productions from family groups, for whom it represents an important
source of income. Agroindustrial producers usually claim select species where just
the leaves or another aerial part are employed, but it’s quite common to notice the
trading of underground parts like roots or rhizomes and roots barks, as observed in
Boerhavia diffusa, Cayaponia espelina, Herreria montevidensis, Jatropha isabelli,
among many others, with a high risk of overexploitation. The use of other parts
like the aerial parts or flower tops allows the reproduction of such species (Degen
et al. 2004).
The work performed on Itá Azul and San Gervasio communities revealed
that the medicinal plants employed by the population have several sources, i.e.,
50% and more were autochthonous species mostly consumed as fresh herbs and
collected from the wild; following this group are introduced species which are
cultivated around the houses only for family consumption, and finally are those
imported species locally available as dried herbs in the stores. They also mentioned
a few native species being grown because of their shortage in the wild, like Piper
regnellii, which was included in the list of threatened species elaborated by the
National Environmental Secretary (SEAM) (2006), or Stevia rebaudiana, being
currently absent in its natural habitat, but widely cultivated for industrial purposes.
Another species severely compromised as a consequence of overexploitation is
Maytenus ilicifolia, since its root bark is the most requested part. Collectors harvest
very small plants, which results in very low development, placing the species in
a critical conservation status. Achyroclyne alata can also be mentioned, since this
native species is present only in certain regions of the country, which moves the
inhabitants of rural communities to buy it for personal use (Degen and González
2014b, Degen et al. 2004).
The continuous pressure on medicinal plants in their habitat motivated
research efforts in order to initiate acclimation studies to contribute to their
preservation and to encourage sustainable production. As a result of such efforts,
the successful development in controlled conditions of three medicinal species
Ethnobotanical Issues on Medicinal Plants from Paraguay 247
González et al. (2009b), González et al. (2011), Degen et al. (2011), Degen et al.
(2012a), Degen et al. (2012b), González et al. (2014) and González et al. (2016).
This kind of research has also been performed in the Biology Department of the
Faculty of Exact and Natural Sciences (Facultad de Ciencias Exactas y Naturales,
UNA), resulting in the anatomical description of Stevia rebaudiana, Tagetes
minuta, Pterocaulon polystachyum (Asteraceae), and Laurus nobilis (Lauraceae),
among others (Benítez et al. 2010, Pereira et al. 2011, González and Pereira 2012,
González et al. 2015).
Based on the number of plant species currently employed for medicinal
purposes in Paraguay, it is evident that much work still needs to be done concerning
morphology and anatomy studies of our plants.
to study the effects of medicinal plants on the central nervous system and the animal
behavior in the search of molecules acting as sedative, anxiolytic, antidepressant,
antipsychotic and anticonvulsant. Such studies started with the analysis of biological
properties of Kyllinga brevifolia and Aloysia polystachya, and more recently, they
kicked off the evaluation of activity on the digestive tract, either gastroprotective
or hepatoprotective in A. polystachya and Sida rhombifolia. Some efforts were also
directed to perform the experimental validation of species traditionally employed
to treat diabetes, like Prosopis ruscifolia and Cyclolepis genistoides (Ibarrola and
Degen 2011).
A very good example of a multidisciplinary evaluation process on medicinal
plants was achieved by the researchers from the FCQ, which have obtained relevant
results from preclinical essays with Solanum sisymbriifolium, demonstrating low
toxicity, little effects on animal behavior and an important decrease of arterial
pressure (Ibarrola et al. 1996, 2006); furthermore, bioassay-guided isolation was
conducted for identification of two closely related spyrostannic monodesmosidic
saponins: isonuatigenoside (Fig. 12.11)—a new chemical structure (Ferro et al.
2005), and nuatigenoside (Fig. 12.12). Recently, these are recognized as the most
active isolated metabolites, allowing to establish a close correlation between the
activity of the metabolites and the popular use of the plant (Ibarrola and Degen
2011).
Facing the required social and productive projection of the knowledge acquired
from medicinal plants, new routes to catch the interest of local pharmaceutical
and nutraceutical enterprises were explored through innovation projects. A good
example was the development of a standardized protocol for the sustainable
production of a phytomedicine based on the experimental evaluation of Aloysia
polystachya as an antidepressant, which included botanical, chemical and
pharmacological evaluations.
At the present time, bioprospective research projects on medicinal plant species
are being conducted, along with their chemical, pharmacological and toxicological
evaluations, comprising species from Euphorbiaceae, Solanaceae, Verbenaceae,
Moraceae and Lorantaceae families, among others.
Fig. 12.11. Isonuatigenoside (Ferro et al. 2005, Structure elaborated by Amner Muñoz Acevedo).
250 ETHNOBOTANY: Local Knowledge and Traditions
Fig. 12.12. Nuatigenoside (Mimaki et al. 1995, Structure elaborated by Amner Muñoz Acevedo).
Conclusions
Paraguay is a country that has very rich flora, with a variety of native traditions
from both indigenous and European origin: some are autochthonous and others are
shared with other Latin America countries. Among these traditions, those related to
medicinal plants are remarkable and closely related to the native heritage. Medicinal
plants are employed either as fresh or dried plant material, consumed together
with “mate” or “tereré” as refreshment beverages and to treat different ailments,
especially those from digestive and respiratory tracts, but also to treat chronic health
conditions like diabetes or hypertension. This mode of employment reaches the
whole population, across different social classes, and it is getting stronger rather
than being lost. Medicinal plants are a relevant option to develop innovative drugs,
which could result in safer and more effective treatments compared to synthetic
drugs. However, the challenges concerning medicinal plants go further than
validation of traditional knowledge, and should face their transformation into safe
drugs. These challenges include critical issues, like those related to the sustainable
exploitation of the natural resources preserving the availability of highly demanded
plant material without the risk of extinction. Other issues to be addressed are those
related to the recognition of the intellectual rights of native populations, in order
to return a part of the economic benefits and royalties resulting from the trading
of drug developed from traditional medicinal plants, the tracing of raw material
in the productive processes, and the strengthening of multidisciplinary research
teams, with both the human and material resources required for the production of
new knowledge. Such efforts are required to succeed in the race against the menace
of losing traditional heritage and biodiversity, just to mention some critical issues.
Acknowledgments
The authors thank the institutions that have supported the research on medicinal
plants at the Facultad de Ciencias Químicas, UNA, as the Research Direction
of the Universidad Nacional de Asunción, JICA, CONACYT, Tropical Forest
Conservation Fund-Paraguay, CYTED, FIDA and FUNDAQUIM.
Ethnobotanical Issues on Medicinal Plants from Paraguay 251
They also thank José Luis Martinez for the invitation to participate in this
project, building up an important platform to disseminate the knowledge related
to medicinal plants, and to Lic. Gabriela Ferro for her kind revision of the English
translation.
References
Achucarro, C., Ferro, E.A., Richer, Y., Salazar, M.E., Ciciolli, S., Ortiz, I., Campos, S., Sckell, C.,
Samudio, M., Alborno, R.M., Meza, B., Varela, I., Losanto, J. and Pedrozo, J.R. 2011. Evaluación
clínica preliminar del efecto antiparasitario de Stevia rebaudiana Bertoni (ka`a he ê) en adultos
y niños. An. Fac. Cienc. Méd. 44(2): 35–46.
Alvarenga, N.L., Velázquez, C.A., Gómez, R., Canela, N.J., Bazzocchi, I.L. and Ferro, E.A. 1999. A new
antibiotic nortriterpene quinone methide from Maytenus catingarum. J. Nat. Prod. 62(5): 750–751.
Alvarenga, N.L., Ferro, E.A., Ravelo, A.G., Kennedy, M.L., Maestro, M.A. and González, A.G. 2000.
X-ray analysis of Volubilide, a new decacyclic Diels-Alder C20–C30 aduct from Hyppocratea
volubilis L. Tetrahedron 56: 3771–3774.
Alvarenga, N., Canela, N.J. and Torio, H. 2008. Composición química y actividad antifúngica del aceite
esencial de hojas de Lippia alba, Verbenaceae. Rojasiana 8(1): 39–42.
Armadans, A. 2010. Estudiantes de la FCA presentaron en público trabajos de investigación y tesis.
Congreso Nacional de Ciencias Agrarias. Available at: http://www.agr.una.py/Difusion/imagen/
boletines/boletinfca10.pdf. Consultado el 10 de abril de 2016.
Arenas, P. and Moreno Azorero, R. 1976. Plantas usadas en la medicina folklórica paraguaya para
regular la fecundidad. Rev. Soc. Cient. Paraguay 16: 21–43.
Arenas, P. and Moreno Azorero, R. 1977. plants used as jeans of abortion, conception, sterilization and
fecundation by paraguayan indigenous people. Econ. Bot. 31: 306–306.
Avilla, J., Teixidó, A., Velázquez, C., Alvarenga, N., Ferro, E.A. and Canela, R. 2000. Insecticidal activity
of Maytenus species (Celastraceae) nortriterpene quinone methides against codling moth, Cydia
pomonella (L.) (Lepidoptera: Tortricidae). J. Agricultural & Food Chemistry 48: 88–92.
Basualdo, I., Soria, N., Ortiz, M., Acosta, L., Degen, R. and Eliceche, A. 1992. Plantas tóxicas para
el ganado en los Departamentos de Concepción y Amambay, Paraguay. Editorial EDUNA.
Asunción-Paraguay, pp. 129.
Basualdo, I. 1993. Teodoro Rojas, un ilustre botánico paraguayao. Rojasiana 1(1): 1–2.
Basualdo, I. and Soria, N. 1996a. Plantas aromáticas de la medicina folclórica paraguaya. Anales de
SAIPA. Sociedad argentina para la investigación de productos aromáticos 14: 57–62.
Basualdo, I. and Soria, N. 1996b. Farmacopea herbolaria paraguaya: especies de la medicina folklórica
utilizadas para combatir enfermedades del tracto respiratorio (Parte I). Rojasiana 3(2): 197–238.
Basualdo, I., Soria, N., Keel, S. and Rivarola, N. 1997. Recursos fitogenéticos, Parque Naiconal Cerro
Corá – Amambay. Plantas útiles. Dirección de Parques Nacionales y Vida Silvestre, Facultad
de Ciencias Químicas – Universidad Nacional de Asunción, The Nature Conservancy (USA).
Asunción. 75 pp.
Basualdo, I., Soria, N., Ortiz, M. and Degen, R. 2003. Uso medicinal de plantas comercializadas en
los mercados de Asunción y Gran Asunción, Paraguay. In: Revista de la Sociedad Científica del
Paraguay 14: 5–22.
Basualdo, I., Soria, N., Ortiz, M. and Degen, R. 2004. Plantas medicinales comercializados en los
mercados de Asunción y Gran Asunción. Rojasiana 6(1): 95–114.
Benítez, L.G. 1986. Breve historia de grandes hombres. Industrial Gráfica Comuneros, Asunción,
Paraguay. 390 pp. Disponible en: http://www.portalguarani.com/1484_luis_g_benitez/14151_
breve_historia_de_grandes_hombres_obra_de_luis_g_benitez_.html. Consultado el 1 de abril
de 2016.
Benítez, B., Pereira, C., González, F., Molinas, C. and Bertoni, S. 2010. Morfología y micrografía
del ka’a he’e, Stevia rebaudiana (Bertoni) Bertoni, provenientes de cultivares de Concepción,
Paraguay. Steviana 2: 55–67.
252 ETHNOBOTANY: Local Knowledge and Traditions
Bertoni, M. 1927. La medicina Guaraní. Conocimientos científicos. Imp. y Edit. Ex-Sylvis, Alto Paraná,
Paraguay. 299 pp. Disponible en: http://www.mag.gov.py/bina/dato/La%20Medicina%20Guarani.
pdf. Consultado el 5 de mayo de 2016.
Canela, N., Alvarenga, N.L., Ferro, E.A., Vila, R. and Cañigueral, S. 2004. Chemical composition of the
essential oil of Aristolochia giberti Hooker from Paraguay. J. Essential Oil Research 16: 566–567.
Céspedes de Zárate, C., González, G., Delmás de Rojas, G., Vogt, C. and Quiñonez, P. 2007. Aclimatación
de tres especies de uso en medicina popular con rango de amenaza. Rev. Investigaciones y estudios
en la UNA 3: 63–74.
Céspedes de Zárate, C., González, G. and Delmás de Rojas, G. 2014. Producción de raíces de Herreria
bonplandii, lecomte y H. montevidensis Klotzch ex Griseb., “zarzaparrilla”, especies utilizadas
en medicina popular, Paraguay. Rojasiana 13(2): 25–33.
Degen, R. 1990. Los nombres vulgares y científicos en la taxonomía botánica. La Revista Crítica 2(4):
60–65.
Degen, R., Basualdo, I. and Soria, N. 2004. Comercialización y conservación de especies vegetales
medicinales en Paraguay. Revista Fitoterapia 4(2): 129–138.
Degen, R., Soria, N., Ortiz, M. and Basualdo, I. 2005. Problemática de nombres comunes de plantas
medicinales comercializadas en Paraguay. Dominguezia 21(1): 11–16.
Degen de Arrúa, R.L., González, Y.P. and Amarilla, A. 2009. Legislación sobre Plantas Medicinales
y Fitoterápicos en Paraguay: una tarea pendiente. Bol. Latinoam. Caribe Plant. Med. Aromat.
18(1): 12–16.
Degen, R., González, Y. and González de García, M. 2011. Análisis de la yerba mate elaborada
compuesta, comercializada en Asunción y Gran Asunción, Paraguay. Rojasiana 10(2): 81–91.
Degen de Arrúa, R., González, Y., González de García, M. and Delmás de Rojas, G. 2012a. Morfoanatomía
comparativa de dos especies de Acanthospermum (Asteraceae). Rojasiana 11(1-2):67–78.
Degen, R., Mercado, M.I., Coll Aráoz, M.V., Ruiz, A. and Ponessa, G.I. 2012b. Morfología y anatomía
de dos variedades de Begonia cucullata (Begoniaceae) comercializadas como «agrial» en Paraguay.
Lilloa 49(2): 87–97.
Degen, R. and González, Y. 2014a. Plantas medicinales utilizadas en la medicina popular paraguaya
como antiinflamatorias. Bol. Latinoam. Caribe Plant. Med. Aromat. 13(3): 213–231.
Degen de Arrúa, R. and González, Y. 2014b. Plantas medicinales utilizadas en las comunidades de Itá
Azul y San Gervasio, (Paraguay). Revista de Fitoterapia 14(2): 33–47.
Feliciangeli, R. 1939. Proyecto de la Farmacopea Paraguaya. La Colmena S.A.: Asunción. Tomo III:
168–182.
Ferro, E.A., Alvarenga, N.L., Ibarrola, D.A., Hellion-Ibarrola, M.C. and Ravelo, A.G. 2005. A new
steroidal saponin from Solanum sisymbriifolium roots. Fitoterapia 76: 577–579.
Ferro, E. and Degen de Arrúa, R.L. 2011. Actividad Inhibitoria de Extractos de Plantas Medicinales de
Paraguay sobre Aldosa Reductasa de Cristalino de Rata. Rojasiana 10(2): 31–42.
Freixa, B., Vila, R., Ferro, E.A., Adzet, T. and Cañigueral, S. 2001. Antifungal principles from Piper
fulvescens. Planta Med. 67(9): 873–5.
Gonzalez Torres, D. 1992. Catálogo de plantas medicinales (Utiles y Alimenticias) usadas en Paraguay.
Asunción. 456p
González, F. and Pereira, C. 2012. Morfoanatomia foliar y caulinar de Tagetes minuta L. (suico)
comercializada como medicinal. Libro de resúmenes de las I Jornadas Paraguayaas de Botánica.
Pág.: 18.
González, F., Benítez, B. and Soria, N. 2015. Morfoanatomía cualitativa foliar y caulinar de Pterocaulon
polystachyum DC. (Asteraceae), de uso medicinal en Paraguay. Steviana 7(supl.): 25.
González, G. and Degen de Arrúa, R. 2015. Capítulo V: Fotalecimiento y uso sostenible (Vivero).
Capitulo V. Conservación, Fortalecimiento y uso sostenible de la Flora de Itá Azul, Colonia
Independencia, Paraguay. Fondo de Conservacion de Bosques Tropicales, Facultad de Ciencias
Químicas, FUNDAQUIM. 85–105 p.
González, M., González, Y. and Degen, R. 2009a. “Yerba mate”, Ilex paraguariensis A. St-Hil. var.
paraguariensis (Aquifoliaceae) caracteres exo-endomorfológicos y farmacognósticos. Rojasiana
8(2): 39–51.
Ethnobotanical Issues on Medicinal Plants from Paraguay 253
González, M., Brítez, L., González, Y. and Degen, R. 2011. Morfoanatomía comparativa de Genipa
americana L. (Rubiaceae) y Sorocea bonplandii (Baill.) W.C. Burger, Lanj. & Wess. Boer
(Moraceae). Rojasiana 10(1): 93–101.
González, Y. and Degen, R. 2008. Morfoanatomía comparativa de las especies comercializadas como
“kapi’i kati” en los mercados de Asunción y San Lorenzo, Paraguay. Rojasiana 8(1): 43–47.
González, Y., Degen, R. and Delmás, G. 2008. Estudio morfoanatómico de “salvia” Lippia alba (Miller)
N.E. Brown (Verbenaceae). Rojasiana 8(1): 93–95.
González, Y., Mercado, M.I., Degen, R. and Ponessa, G. 2009b. Morfoanatomía y etnobotánica de
rizoma, tallo y escapo de “kapi’i kati”, Kyllinga odorata (Cyperaceae) y sus sustituyentes, de
Asunción y alrededores, Paraguay. Lilloa 46(1-2): 58–67.
González, Y., Degen, R., González, G. and Delmás, G. 2013. Especies medicinales, su estado de
conservación y usos, de la Compañía Pikysyry, Departamento de Cordillera, Paraguay. Rojasiana
12(1-2): 105–115.
González, Y., Degen de Arrúa, R., Delmás de Rojas, G. and González de García, M. 2014.
Etnofarmacobotanica foliar de burrito, Aloysia polystachya (Griseb.) Moldenke (Verbenaceae)
cultivado en Paraguay. Rojasiana 13(1): 31–41.
González, Y., González de García, M., Delmás de Rojas, G. and Degen de Arrúa, R. 2016. Morfología
y anatomía de Phyllanthus orbiculatus (Phyllanthaceae) comercializada como «para para’í» en
Paraguay y sus posibles sustituyentes. Lilloa 53(2): 217–228.
Gupta, M. 1995. 270 plantas medicinales iberoamericanas. Convenio Andrés Bello-CYTED. Ed.
Presencia Ltda. Santa Fe de Bogotá, Colombia, pp. 617.
Gupta, M. 2008 (ed.). 500 Plantas Medicinales iberoamericanas. CYTED. Convenio Andrés Bello.
1003 pp.
Heck, C.I. and De Mejia, E.G. 2007. Yerba Mate Tea (Ilex paraguariensis): A comprehensive
review on chemistry, health implications, and technological considerations. J. Food Sciences
72(9): R138–R151.
Ibarrola, D.A., Hellión, M.C. and Ferro, E.A. 1996. The hypotensive effect of the crude root extract
of Solanum sisymbriifolium Lam. In normo and hypertensive rats. Journal of Pharmaceutical
Biology 44(5): 378–381.
Ibarrola, D.A., Hellión, M.C., Ferro, E.A., Hatakeyama, N., Shibuya, N., Yamazaki, M., Momose, Y.,
Yamamura, S. and Tsuchida, K. 2006. Cardiovascular action of nuatigenosido from Solanum
sisymbriifolium. Journal of Pharmaceutical Biology 44(5): 378–381.
Ibarrola, D.A. and Degen de Arrúa, R.L. (eds.). 2011. Catálogo ilustrado de 80 plantas medicinales
del Paraguay. Facultad de Ciencias Químicas-UNA y Agencia de Cooperación Internacional del
Japón-JICA, Asunción, Paraguay, pp. 1–178.
MAG-DGPE. 2008. Informe Final. Elaboración del Estudio de la Situación de la Recolección, Producción
y Comercialización de Plantas Medicinales y Aromáticas de Paraguay. Programa Regional de
Apoyo a la Red de Desarrollo de Fitoterápicos en el MERCOSUR. 1–189.
Maidana, M., Gonzalez, Y. and Degen de Arrúa, R. 2015. Plantas medicinales empleadas por pacientes
diabéticos en Paraguay. Infarma 27(4): 218–224.
Masulli, B., Mereles, F., Aquino, A., Gamarra, I., Medina, F., Rossato, V., Sottoli, S. and Vera, V.
1996. El rol de la mujer en la utilización de los recursos naturales en el Paraguay: Un enfoque
multidisciplinario. 1–247.
Mereles, F. and Degen, R. 1994a. Leñosas de uso popular en chaco boreal. Revista forestal del Paraguay,
Universidad Nacional de Asunción 10(1): 14–19.
Mereles, F. and Degen, R. 1994b. Los nombres vulgares de los árboles y arbustos del Chaco Boreal,
Paraguay. Rojasiana 2(2): 67–101.
Mereles, F. and Degen, R. 1997. Contribución al conocimiento de los árboles y arbustos indígenas
utilizados como medicinales en el Chaco Boreal (Paraguay). Parodiana 10 (1-2): 75–89.
Mereles, F. 2001. Recursos Fitogenéticos: Plantas útiles de las cuencas del Tebicuary mi y Capiíbary,
Paraguay Oriental. Proyecto Sistema Ambiental de la Región Oriental, (SARO). Rojasiana, Vol.
Esp. 144 pp.
Mereles, F. 2006. La diversidad, los usos y la conservación de las especies vegetales en los humedales
del Paraguay. Rojasiana 7(2): 171–185.
254 ETHNOBOTANY: Local Knowledge and Traditions
Mereles, F. 2014. Una aproximación al estado ambiental del Paraguay. pp. 127–140. In: Segundo
Simposio internacional. Hacia nuevas políticas culturales. Centro Cultural de la República.
Paraguay.
Mimaki, Y., Nakamura, O., Sashida, Y., Nakaido, T. and Ohimoto, T. 1995. Phytochem. 385: 1279–1286.
Ortiz, M., Degen, R. and Benítez, M.C. 1993. Tricomas glandulares en hojas de Heliotropium procumbens
Miller. Rojasiana 1(1): 16–20.
Ortiz, M. and Delmás, G. 1997. Anatomía foliar de tres especies utilizadas en la medicina folklórica
paraguaya. Rojasiana 4(1): 1–10.
Pin, A., González, G., Marin, G., Céspedes, G., Cretton, S., Christen, P. and Rouget, D. 2009. Plantas
medicinales del Jardín Botánico de Asunción. Municipalidad de Asunción, AEPY y Universite
de Geneve. 1–441.
Pereira, C., González, F. and Benítez, B. 2011. Micrografía foliar de Laurus nobilis L. (Lauraceae)
como herramienta para el control de calidad de muestras comerciales. Boletín de la Sociedad
Argentina de Botánica 46(Supl.): 114.
Polini, G., López Ramírez, A., Degen de Arrua, R., Quarti, A., Delmás de Rojas, G., González, Y. and
Aquino, O. 2013. Comer Del Monte, Plantas Medicinales Del Chaco Central. ISBN 978-99967-
611-2-6. 352 pp.
Resquin Romero, G.A. 2011. Producción sostenible de Menta Mentha arvensis y Mentha x piperita
en sistemas de agricultura familiar campesina de la Región Oriental, Paraguay. FCA-UNA/
CONACYT/CETEC. 235 p.
Resquín, G., Degen de Arrúa, R., Delmás de Rojas, G. and Macchi Leite, G. 2011. Las especies de
Mentha L. cultivadas en Paraguay. Rojasiana 10(1): 77–91.
Riveros, R., González, Y., González, M. and Degen, R. 2009. Etnofarmacobotánica de “Jagua rová”,
Jatropha isabelli Mull. Arg. Rojasiana 8(2): 25–30.
Scavone, C. 2011. Plantas medicinales: un poco de historia. Artículo en ABC Edic. Impresa. 27 de
abril de 2010. Disponible en: http://www.abc.com.py/articulos/plantas-medicinales-un-poco-de-
historia-95752.html. Consultado el 15 de abril 2016.
Schinini, A. 2005. Teodoro Rojas, biografía, viajes y especies dedicadas. Rojasiana 7(2): 101–149.
Schmeda, G. and Silva, M. 1982. The flavonoids of Eupatorium laeve DC. Compositae. Publicaciones
FCQ N° 5.
Schmeda Hirschmann, G., Ferro, E.A., Franco, L., Recalde, L. and Theoduloz, C. 1987. Pyrrolizidine
Alkaloids from Senecio brasiliensis Populations. J. Nat. Prod. 50(4): 770–772.
SEAM (Secretaría del Ambiente). 2006. Resolución 524/06 por la cual se aprueba el listado de especies
de flora y fauna amenazadas del Paraguay.
Soria, N. 1993. Las especies aladas de Baccharis utilizadas como medicinales en Paraguay. Rojasiana
1(1): 3–12.
Soria, N. and Basualdo, I. 2005. Medicina herbolaria de la Comunidad Kavajú Kangué, Departamento
de Caazapá. 1–138.
Soria, N., Basualdo, I. and Ortiz, M. 2006. Las especies medicinales de los humedales en Paraguay.
Rev. Soc. Cient. Paraguay 20: 94–112.
Soria, N. and Ramos, P. 2015. Guía para el uso de plantas medicinales en atención primaria de salud,
Paraguay. Editorial Académica Española. 1–127.
Theoduloz, C., Franco, L., Ferro, E.A. and Schmeda-Hirschmann, G. 1988. Xanthine oxidase inhibitory
activity of paraguayan Myrtaceae. J. Ethnopharmacology 24: 179–183.
Vargas Lehner, F. (Coord.). 2013. Producción de plantas medicinales: burrito, menta, orégano. Proyecto
Financiado por la comunidad europea. Facultad de Ciencias Agrarias. San Lorenzo.
Vera García, R., Peralta, I. and Caballero, S. 2005. Fraction of minerals extracted from Paraguayan
yerba mate Ilex paraguariensis, by cold tea, maceration and hot tea infusion as consumed in
Paraguay. Rojasiana 7(1): 21–25.
Vera Jiménez, M. 2009. Plantas medicinales de tres áreas silvestres protegidas y su zona de influencia
en el sureste de Paraguay. Fundación Moisés Bertoni. Asunción, Paraguay. 1–160.
Vera Jiménez, M. 2011. 30 plantas medicinales utilizadas en fitoterapia. Fundación Moisés Bertoni,
Mancomunidad Mbaracayú y Asociación Etnobotánica Paraguaya. 1–40.
CHAPTER 13
An Overview of Vetiveria
zizanioides (Linn.) Nash (Poaceae)
Traditional Uses and Products
Shubhangi N. Ingole
Introduction
The world is endowed with a rich wealth of medicinal plants and India is sitting on
a gold mine of well recorded and traditionally well-practiced knowledge of herbal
medicine. More than 1500 herbal preparations are sold as dietary supplements or
ethnic traditional medicines (WHO 2000). India is perhaps the largest producer of
medicinal herbs and is rightly called the botanical garden of the world (Parrotta
2001). India is well known as an emporium of medicinal plants (Rao et al. 2016).
The herbal drugs provide an alternative and effective treatment for chronic disorders
(Astin 1998, Cupp 1999).
Man cannot survive on this earth for a long time without the plant kingdom
because the plant products and their active constituents play an important role. The
herbal medicines as the major remedy in traditional medical systems have been used
in practice for thousands of years. Herbs have always been the principal form of
medicine in India and presently they are becoming popular throughout the world.
These have made a great contribution in maintaining human health. Plants as a
source of medicine have been playing an important role in health services around the
globe and constitute the backbone of the herbal medicine (Shankar and Liao 2004).
But India despite its rich traditional knowledge, heritage of herbal medicines
and large biodiversity has a dismal share in the world market due to export of crude
extracts and drugs (Kamboj 2000, Desmet 2002, Dubey et al. 2004). Hence, today
Department of Botany, Bar. R.D.I.K. and N.K.D. College Badnera-Amravati, Maharashtra, India.
Email: [email protected]
256 ETHNOBOTANY: Local Knowledge and Traditions
Sub-division: Monocotyledons
Series: Glumaceae
Family: Poaceae
Sub-family: Andropogoneae
Genus: Vetiveria
Spp.: zizanioides
Synonyms
Andropogon muricatus Retz., A. squarrosus Hook. f., non Linn. F., Anatherum
zizanioides (Linn.) Hitchcock and Chase.
Sanskrit Synonyms
• Nalada, Amrnala, Veerana, Virani, Veeratara, Valaka, Balaka Truna Valukam,
Veniga Mulakam Abhaya, Ranapriya, Virataru, Haripriya Jalvasa, Jalaamoda,
grows in moist places.
• Amrunala, Mrunalaka – Appears similar to Lotus stalk.
• Sugandhika, Samagandika, Sugandhamula – Has a pleasant odor.
• Bahumoola – Bushy roots.
• Shishiram, Sheetmoola – root is a coolant.
• Sevya – suitable for consumption.
There are many ecotypes of vetiver. The vetiver called VS-01 (or sunshine) is
a south Indian variety, has robust root system, and has 1% aromatic oils in its roots.
Other varieties like VS-03 have less aromatic oil content (around 0.3%). Research
has shown that the aromatic oil is produced in the roots by certain bacteria from
precursors released by the vetiver. It is just to say that all vetiver roots are not the
same.
Vetiver roots treat the mother earth too. It is perhaps mentioned in Krishi
Shastra. Vetiver roots increase the ground water recharge capability of soils. It
increases the biomass content in the soil up to 3 meters depth. It will be very
difficult to add leaves and manure at that depth. Vetiver roots add the biomass as
roots, and they decay after 18 months. Vetiver root oil is termite-repelling. The
vetiver root system increases the aeration in the soil, it also play ecological role by
helping to stabilize soil, protects it against erosion and prevents nematode (small
worms that attack the roots and other plants) infection. Because of these effects,
vetiver is grown as rows along vegetable farms, and around trees in orchard which
improves the health and yield of the cultivated crops. Thus, growing neem, tulsi
and vetiver in farms and around houses is good for the health of the plants and
animals in the earth.
Two species of Vetiveria are found in India, of which Vetiveria zizanioides is the
common source of the well known oil of Vetiver, which is used in medicine and in
perfumery. Khas grass grows wild in many states, namely Haryana, Uttar Pradesh,
258 ETHNOBOTANY: Local Knowledge and Traditions
Rajasthan, Gujarat, Bihar, Orissa and Madhya Pradesh and throughout South India.
It is systematically cultivated in the North Indian states of Rajasthan, Uttar Pradesh
and Punjab and in the South Indian states of Kerala, Tamil Nadu, Karnataka and
Andhra Pradesh. The yield from the cultivated crops, however, meets only a very
small percentage of the requirements of the country. The bulk of the roots used
for cooling purposes and for the extraction of the oil are obtained from the wild.
It is also cultivated for the fragrant essential oil distilled from its roots and
used in high end perfumes. Worldwide production is estimated at about 250 tons
per annum. The oil is amber brown and rather thick.
History
It has been known to India since the ancient times. It has been considered as a high
class perfume. Copper plate inscriptions listing the perfume as one of the articles
used by royalty have been discovered. In Ayurvedic literature, it is called ‘Suganti-
mulaka’ (meaning sweet smelling) and ‘sita-mulaka’ (having cool roots). All over
India, the roots are made into scented mats, fans, ornamental baskets and many
other articles and also burnt as a fumigatory. The aromatic roots are made into
bundle and kept in water vase to impart aroma to water and getting cooling effect.
It is also put into cold beverages like unripe mango juice or Indian cold drinks to
impart its taste and coolness.
Morphological Description
It is densely tufted grass. The culms are arising from an aromatic rhizome. The
grass is stout, up to and over 2 m tall, in dense tufts, with stout spongy aromatic
roots. The leaves are narrow, erect, keeled, glabrous and its margins are scabrid. The
An Overview of Vetiveria zizanioides (Linn.) Nash (Poaceae) 259
Chemical Constituents
Principal constituents of oil are d and p vetivone, zizanal and epizizizanal,
vetiselimenol, Khisumol, Allokhusiol, Benzoic acid, Cyclocapacamphene,
Epikhusinol, 2-epizizanone, B-eduesmol, Eugenol, Iskhusimol, Isokhusinoloxide,
Isovalencenol, Isovalencic, Khusimyl acetate, Khusinodiol, Khusinol, Khusitoneol,
Laevojujenol, Levojunenol, Vanillin, Vertiselinenol, B-& J. Vetivene, Vetivenic
acid, vetiverol, zizaene, Zizanol, etc. which were isolated from the oil. Due to the
presence of these chemicals, it has its pharmacological properties (Mishra et al.
2013, Pareek and Kumar 2013).
260 ETHNOBOTANY: Local Knowledge and Traditions
Pharmacology
Zizanal and epizizanal exhibited insect repellent activity.
Parts Used
Roots, vetiver oil.
Doses
Powder 3–6 gm, decoction 15–100 ml, infusion 25–50 ml.
Medicinal Properties
Rasa (taste) – Tikta (bitter), Madhura (Sweet), Guna (qualities), Rooksha (dryness),
Laghu (Lightness), Vipaka – Katu – undergoes pungent taste conversion after
digestion, Veerya – sheeta – cold potency effect on tridosha – pacifies vata and pitta.
Uses
Khas grass has variety of uses from household to therapeutic.
Ethnomedicinal Uses
About 70% of rural folk depend on medicinal plants for their healthcare. Since
ancient times, ethnobotanical use of plants has been known and use of traditional
medicine and medicinal plants in most developing countries as therapeutic agents
for the maintenance of good health has been widely observed and accepted (Rao
et al. 2016).
Various tribes use the different parts of the grass for many of their ailments such
as mouth ulcer, fever, boil, epilepsy, burn, snakebite, scorpion sting, rheumatism,
fever, headache, etc. The Santhal tribes of Bihar and West Bengal use the paste
of fresh roots for burn, snakebite and scorpion sting, and a decoction of the roots
as a tonic for weakness; in West Bengal, the tribal people use the root paste for
headache, rheumatism and sprain, and a stem decoction for urinary tract infection;
in Madhya Pradesh, the leaf juice is commonly used as anthelmintic; the tribes
of the Varanasi district inhale the root vapor for malarial fever. The root ash is
given to patients for acidity by the Oraon tribe. Likewise, there are many different
applications of the plant for different ailments among different ethnic tribes (Singh
and Maheshwari 1983, Jain 1991).
Decoction of the rhizome is taken internally to treat blood pressure and stomach
ache problems in Kumargiri Hills, Tamil Nadu (Kam and Alagesaboopathi 2009).
A decoction of leaves is recommended as a diaphoretic. When locally applied in
rheumatism, lumbago and sprain, it is good ambrocation and affords relief. In M.P.,
the plant is used as an anthelmintic for children. The oil is reported to be used as a
An Overview of Vetiveria zizanioides (Linn.) Nash (Poaceae) 261
Anti Inflammatory
The very soothing and cooling effect of this essential oil calms and pacifies all sorts
of inflammations. But it is particularly good in giving relief from inflammations in
circulatory system and nervous system. It is found to be an appropriate treatment
for inflammations caused by sun stroke, dehydration and loo (name given to very
hot and dry winds prevalent during summers in the dry regions of India and few
neighboring countries).
Antiseptic
In tropical countries like India and its neighbors, microbes and bacteria grow
very fast due to their favorable hot and humid climate found in this region. Then
it becomes obvious that your wounds are most likely to get septic in these places
since there are plenty of bacteria here. But Mother Nature is very kind and she has
provided the remedies too, right in those places. One such remedy is this Vetiver
and the essential oil extracted from it. This oil efficiently stops the growth of
Staphylococcus aureus, the bacteria responsible for causing septic, and eliminates
them, thereby helping cure septic and giving protection against it. Being totally
safe, this oil can be applied externally on wounds or taken orally, to protect wounds
as well as internal organs from septic.
Aphrodisiac
Mixed in sorbets and beverages as a flavoring agent, this oil has an aphrodisiac
effect. It enhances libido and gives arousals. Since sex has more to do with the
psychology (brain) than the physiology, remedy for most of the sexual disorders
like frigidity, lack of libido, impotence, etc. lays in the brain. Certain components
of this oil stimulate those portions of brain and the problems are over.
262 ETHNOBOTANY: Local Knowledge and Traditions
Cicatrisant
Cicatrisant is a property by virtue of which a substance speeds up the eradication
or disappearance of the scars and other marks from the skin. It promotes growth
of new tissues in the affected places which replace the dead and discolored tissues
and helps achieve a uniform look. This is also useful for the post delivery stretch
marks, fat cracks, after spots left by pox, burns, etc.
Nervine
A tonic for the nerves is called a nervine, like our Essential Oil of Vetiver is. It takes
care of the nerves and maintains them in good health. It also heals the damages
done to the nerves by shock, fear, stress, etc. Further, it helps get rid of nervous
disorders, afflictions, epileptic and hysteric attacks, nervous and neurotic disorders
such as Parkinson’s Disease, lack of control over limbs, etc.
Sedative
The Essential Oil of Vetiver is a well known sedative. It sedates nervous irritations,
afflictions, convulsions and emotional outbursts such as anger, anxiety, epileptic
and hysteric attacks, restlessness, nervousness, etc. and even benefits patients of
insomnia.
Tonic
The effect of a tonic on the body is quite similar to that of overhauling and servicing
on a vehicle. A tonic tones up every system functioning in the body, namely the
digestive system, respiratory system, circulatory system, excretory system, immune
system, endocrinal system, nervous system and the neurotic system. Thus, in a
nutshell, it keeps the metabolic system in order, rejuvenates the body, gives strength
and boosts immunity.
Vulnerary
This property of Vetiver Essential Oil helps heal wounds by promoting growth of
new tissues at the wounded place and also by keeping it safe from infections by
inhibiting growth of microbes and promoting crowding of leucocytes and platelets
at the place.
Healing
Vetiver essential oil helps in the formation of new tissue and is also used to accelerate
the healing and recovery of skin wounds as well to remove stains, marks on the skin
and the scars themselves. Also, it is used to repair the cracks and grooves in the skin
caused by different circumstances such as pregnancy, diets, allergies, and burns.
An Overview of Vetiveria zizanioides (Linn.) Nash (Poaceae) 263
Calming
In addition to various beverages for culinary purposes and aphrodisiacs, vetiver
essential oil is used to make soothing infusion which is used to relax and recover
from severe strain. It helps to overcome situations of shock, fear, high levels of
stress, panic, etc.
Other Benefits
Other benefits that we tend to award to the use of vetiver essential oil are, for
example, the strengthening of bones, the treatment of rheumatism, gout, arthritis,
muscle aches, dryness, cramps and dry skin (Balasankar et al. 2013).
Ayurvedic Uses
• Pachana – Digestive, relieves Ama dosha,
• Stambhana – blocks, dries up channels,
• Dahahara – relieves burning sensation as in gastritis, neuropathy, burning
sensation in eyes, etc.,
• Madahara – relieves intoxication,
• Jwarahara – useful in fever,
• Trushnahara – relieves thirst,
• Asrajit – useful in blood disorders such as abscess,
• Vshahara – antitoxic,
• Daurgandnyahara – relieves bad odor,
• Mutrakrichrahara – relieves dysuria, urinary retention, acts as diuretic,
• Kushtanut – useful in skin disorders,
• Baminut – relieves vomiting,
• Vranahara – heals wounds quickly,
• Klantihara – relieves tiredness, fatigue,
• Vataghna – Useful in treating disorders of vata dosha imbalance such as
neuralgia, paralysis, constipation, bloating, etc.,
• Mchanut – useful in urinary tract disorders and diabetes,
• Vetiver water – Vetiver is used to make potable water. A few grams of vetiver
root powder is added to water and this water is filtered and used after 2–3
hours. Once the vetiver is put into water, the water should be replaced with
fresh ones. Such prepared water will have almost all the qualities of Khas-
usheer, as explained above, but in slightly lesser intensities.
(www.easyayurveda.com)
External Application
To apply externally as paste, to relieve burning sensation, skin disorders and to
relieve excessive sweating, there is nothing better than khas (Charaka Sutrasthana
264 ETHNOBOTANY: Local Knowledge and Traditions
25). The root powder is made into paste and applied to relieve burning sensation,
burn wounds, to relieve excessive sweetening, in skin disorders and to improve
skin complexion.
Mode of Administration
• Its water can be used as potable water.
• Its powder or water decoction is also used in medicine. It is administered
along with cow ghee, honey, etc., based on disease.
• Its powder is applied externally.
Commercial Products
• Used, Renalka, anti-wrinkle cream, baby powder, gentle baby shampoo, oil
clear mud face pack, purifying neem foaming face wash.
• Vetiver essential oil is used as ingredient in many Ayurvedic medicines such
as Borototal cream.
• Ayurvedic medicines with Khas (Usheera) as ingredient.
• Usheerasava—a fermented medicine used in skin diseases, intestinal worms,
bleeding disorders, etc.
• Shadanga Paniya—A herbal drink used to treat fever.
• Gopanganadi Kashayam—Used in pitta type of fever.
• Nisosiradi oil—An effective Ayurvedic herbal oil used to treat diabetes, car
buncles and abscesses.
• The annual market allotment of vetiver oil.
Country Percentage
USA 40
France 20
Switzerland 12
England 10
Japan 04
Germany 2.4
The Netherlands 02
Countries of vetiver oil origin 12–16
Bioactive Compounds
Roots and leaves show presence of alkaloid, anthracene glycosides, aucubins,
coumarin, emodin, fatty acid, flavonoid, polyuronoid, starch, tannin, reducing
compounds, saponin, steroids, triterpenoids, volatile oil, and protein indicating
the presence of their respective chemical compounds (Kaikade and Ingole 2014,
Savanur 2017).
The GC-MS analysis of roots of Vetiveria zizanioides, which are medicinal
part, revealed the presence of various compounds (phytochemical constituents) at
An Overview of Vetiveria zizanioides (Linn.) Nash (Poaceae) 265
different retention time that could contribute to the medicinal quality of the plant.
The identification of the phytochemical compounds was confirmed based on peak
area, retention time and molecular formula. Its root’s GC-MS analysis shows
presence of dibutyl phthalate (C6H22O4), benzene-dicarboxylic acid (C6H22O4),
diisooctyl phthalate (C24H38O4)—all possessing antimicrobial and antifouling
properties; pthalic acid (C16H26O4); bis (2-methyl propyl) ester; and butyl 2-methyl-
propyl ester. Roots also show presence of Cedren-13-ol (C15H24O) possessing
antioxidant property; antimicrobial, immune-modulatory, anti tumor property;
spathylenol (C15H24O), 12-epoxide (C15H22O2) as building blocks for the synthesis
of a number of pharmaceutical compounds; and H-2-Indenol (C13H22O2).
The phytochemicals identified through GC-MS analysis possess many
biological properties (Kaikade and Ingole 2014).
Table 13.2. List of expected compounds at RT – 13.98.
• Research showed that the Vetiver oil possessed a strong free radical
scavenging activity when compared to standard antioxidants such as butylated
hydroxytoluene (BHT) and α-tocopherol (Kim et al. 2005).
• Antiproliferative Activity
Research showed that Vetiver oil exhibited strong antiproliferative activity
in a pre-inflammed human dermal fibroblast model cells and significantly
inhibited the production of collagen, an important molecule for skin and tissue
remodeling processes (Han and Parker 2017).
• Antibacterial Activity
The antibacterial activity is measured by zone of inhibition (mm). Totally
four bacterial strains (two gram positive S. aureus, B. subtilis and two gram
negative bacteria P. aeurogenosa, E. coli). Ethanolic extract of Vetiveria
Zizanioides is known to posses flavonoids, alkaloids, terpenoids, saponins,
tannins and phenols which, either individually or through combination, exert
antimicrobial activity. The study showed that EEVZ inhibited gram negative
bacteria than grampositive bacteria. Flavonoids are found to be effective
antimicrobial substance against a wide range of microorganisms, probably
due to their ability to complex with extra cellular and soluble proteins and
to complex with bacterial cell wall; more lipophilic flavonoids may disrupt
microbial membrane. Antibacterial activity of tannins may be related to their
ability to inactivate microbial adhesion enzymes and cell envelope transport
proteins; they also complex with polysaccharides. The presence of tannins
present in the roots of Vetiveria zizanioides implied that tannin may be the
active compound which may be responsible for in vitro antibacterial activity
in this study. Tannin in the plant extract was found to possess antibacterial
activity (Devi et al. 2010).
• Hepatoprotective Activity
Methanolic extract of Vetiveria zizanioides Linn is hepatoprotective at the
dose 300–500 mg/kg. The damage induced by ethanol 20% at the dose of
3.75 gm/kg (Chaudhary 2010).
• Antitubercular Activity
The ethanolic extract of intact as well as spent root showed potent
antituberculosis activity at a minimum concentration of 500 μg/mL (Saikia
et al. 2012).
• Mosquito Repellent Activity
In the laboratory oviposition deterrent test, the root extract of Vetiveria
zizanioides at each concentration greatly reduced the number of eggs deposited
by the gravid Anapheles stephens (Arthi and Murgan 2011).
An Overview of Vetiveria zizanioides (Linn.) Nash (Poaceae) 267
• Antihyperglycemic Activity
The effect of root extract of Vetiveria zizanioides in normal fasted rats after
multiple doses showed significant antidiabetic activity at 2nd and 4th hour
after administration compared to diabetic control (Karam et al. 2012).
• Antidepressant Activity
The ethanolic extract of Vetiveria zizanioides possesses antidepressant activity
and the combination of Fluxetine and ethanolic extract of Vetiveria zizanioides
is effective in tail suspension test, and force swim test induced depressive
behavior (Josephine 2012).
• Other Uses
Apart from medicinal uses, there are multiple uses of khas grass in India.
º The culms along with the panicles form a good broom.
º Traditional medicine.
º Roots as water flavoring agents.
º Root mats for door, window screen during summer.
º Socio-economic life of the rural population in India.
º Dried roots for scenting clothes.
º Dried roots for brooms and for thatching.
º Pulp of the plant for paper and straw board.
º Culms and leaves are also extensively used by tribals and villagers for
thatching their huts and mud walls.
º Some Kerala tribes use the mats of the roots and leaves as a bed for a cooling
effect.
Domestic Use
Mats made by weaving Vetiver roots and binding them with ropes/cords are used
in India to cool rooms in a house during summer. The mats are typically hung in
the doorway and kept moist by spraying with water periodically. It acts like an
air-cooler when wind from a fan or outside hits it. It also adds a pleasant aroma in
the house which is commonly described as “cool” and “refreshing”.
Commercial Uses
The commercial applications of the grass mainly pertain to the extraction of Vetiver
oil through distillation of the roots. Vetiver oil is one of the most valuable and
important raw materials in perfumery and finds extensive applications in the soap
and cosmetic industries, for pharmaceutical companies and as antimicrobial and
antifungal agent (Singh et al. 1978, Dikshit and Husain 1984). Over 150 compounds
have been isolated and characterized from Vetiver oil so far. A major portion of oil
consists of sesquiterpene alcohol (Thakur et al. 1989). A major application of the
roots of Vetiver, particularly in North Indian plains, pertains to the preparation and
268 ETHNOBOTANY: Local Knowledge and Traditions
sale of mats/screens for windows, doors and desert coolers during summer months
when the temperature goes up to as high as 45ºC.
As there is no systematic cultivation of the grass in North India, several
villagers and rural folk collect the roots of the grass in large quantities from the
wild growth and flock to the cities where they sell the root mats and loose roots for
flavoring water to city dwellers. 3–4 months of livelihood of several rural families
is sustained by the sale of roots of Vetiver grass playing important role in socio-
economic sector of rural life.
It also plays an ecological role by helping to stabilize soil, protects it against
erosion and also fields against pests and weeds.
Ecosystem management
• Land stabilization.
• Carbon sequestration.
• Pollution control.
Social development
• Employment generation.
• Strengthen coping capacity.
• Community participation (Joseph et al. 2017).
• Private companies and municipalities use Vetiver systems to protect and heal
degraded environments. Vetiver roots absorb pollutants and clarify water.
• As a grass wall and boundary marker, Vetiver hedges are so stable that
surveyors rely on them to establish property lines.
• Between slender rows of Vetiver, farmers can grow crops that benefit from
the accumulation of silt and plant nutrients. Vetiver’s vertical roots nurture
adjacent crops.
• As an excellent batch material—Mature leaves produce long-lasting absorbent
mulch that reduces evaporation and helps mycorrhizae to accumulate.
• As a bios wale—A Vetiver grass channel is an attractive alternative to
traditional concrete drainage ditches, and effectively filters and attenuates
storm water runoff.
• As a constructed wetland- Installed as a leach field, Vetiver absorbs nutrients
generated by cesspools, piggeries, dairy and poultry farms. Vetiver clarifies
effluent and eliminates odors.
• As livestock feed—Vetiver’s nutritional value is similar to Napier grass
(Pennisetum pupureum).
• As a carbon sink—Given the concern regarding global warming and CO2
emissions, 44,500 acres of land protected by Vetiver hedges will provide a
CO2 sink for the carbon produced by 100,000 cars traveling 12,500 miles a
year.
• As biofuels—Leaves can be used as a substrate for ethanol production through
alkali pretreatment followed by enzyme hydrolysis and yeast fermentation,
which generates an ethanol yield of 13% after one-cycle column distillation.
• As a food additive—Vetiver is used domestically in cooking; it’s infused in
tea and also used in baking.
• Handicrafters use Vetiver leaves and roots to create an extensive range of
beautiful woven handicrafts. Like its sister, bamboo, which creates luxurious
textiles, Vetiver would seem suited to produce soft, durable fabric.
• Vetiver is a beautiful ornamental plant for gardens, patios, decks, etc. It forms
a dense, uniform and attractive hedge under tropical and subtropical climates.
It also forms an aesthetically beautiful barrier to unsightly view.
• Agriculture-Related Activities: Used as a Mulch, compost, animal feed,
substrate for mushroom cultivation, botanical pesticides, fungicides, agricides
and weed control (Balasankar et al. 2013).
Vetiver and agroforestry for poverty reduction in third world and natural
resources protection large vetiver nurseries can be developed by farmers for
the sale of planting material to the other farmers and construction agencies for
Vetiver handicraft component industry. Use of vetiver for sustainable environment
particularly in relation to land and water can be recommended.
Vetiver can produce up to 100 tonnes/hectare of biomass (dry weight) within
8 months. The grass is only harvested as a biomass fuel and the perennial vetiver
grass is left in the ground and allowed to grow back year after year lasting forever.
Ecosystem based regional development programs are emerging worldwide
and hence green technologies and systems for the prevention and mitigation of
natural hazards need to be developed. There is a need to highlight the importance
of unique grass like vetiver that has many unique characteristics.
References
Antiochia, R., Campanella, L., Ghezzi, P. and Movassaghi, K. 2007. The use of vetiver for remediation
of heavy metal soil contamination. Anal. Biochem. 388: 947–956. [Google Scholar]
Arctander, S. 1960. Vetiver. Columns. pp. 649–653. In: Perfume and Flavour Materials of Natural Origin.
Elizabeth, New Jersey. Published by the author; printed by Det Hoffensbergske Etablissement,
Denmark.
Arthi, N. and Murgan, K. 2011. Effect of Vetiveria zizanioides L. Asian Pacific Journal of Tropical
Disease 154–158.
Ash, R. and Truong, P. 2003. The use of Vetiver grasswetland for sewerage treatment in Australia. Proc.
Third InternationalVetiver Conf. China, October 2003.
Ashton Lim, Suelee Sharifah, Nur Munirah, Syed Hasan, Fara diella Mohd. Kusin, Ferdaus Mohamat
Yusuff and Zelina Zaiton Ibrahim. 2017. Phytoremediation potential of Vetiver grass (Vetiveria
zizanioides) for treatment of metal contaminated water. Springer International Publishing,
Switzerland 228: 158.
Astin, J. 1998. Why patients use alternative medicines. Results of National Study. J. Ann. Med. Assoc.
279: 1548–1553.
Bajpai, P.N., Singh, I., Tiwari, L.P., Chaturvedi, O.P. and Singh, J.P. n.d. Varietal performance of khus
(Vetiveria zizanioides Stapf.). The Punjab Horticultural Journal n.v.: 208–211.
Balasankar, D., Vanilarasu, K., Selva Preetha, P., Rajeshwari, S., Umadevi, M. and Bhowmik Debjit.
2013. Traditional and medicinal uses of vetiver. Journal of Medicinal Plants Studies 2(3): 191–200.
Bertea, C.M. and Camusso, W. 2002. Anatomy, biochemistry and physiology. pp. 19–43. In: Maffei,
M. (ed.). Vetiveria. The Genus Vetiveria. London and New York: Taylor and Francis Publishers.
[Google Scholar]
Bharad, G.M. and Bathkal, B.C. 1990. Role of vetiver grass in soil and moisture conservation.
In: Proceedings of The Colloquium on the Use of Vetiver for Sediment Control. April 25, 1990.
Watershed Management Directorate, Dehra Dun, India.
Bhatwadekar, S.V., Pednekar, P.R. and Chakravarti, K.K. 1982. A survey of sesquiterpenoids of vetiver
oil. pp. 412–426. In: Atal, C.K. and Kapur, B.M. (eds.). Cultivation and Utilization of Aromatic
Plants. Regional Research Laboratory, Council of Scientific & Industrial Research, Jammu-Tawi,
India.
Bisagacarya. Girindranath. Mukhopadhyaya. 1994. History of indian medicine, New Delhi: Munishiram
Manoharlal publishers pvt LTD, Vol III, 496–499 pp.
Bowen, H.J.M. 1979. Plants and the Chemical Elements. London: Academic Press. [Google Scholar]
Chadha, K.L. 2011. Hand Book of Horticulture,Vetiver, ICAR, New Delhi, 631–632.
Chen, Y., Shena, Z. and Lib, X.D. 2004. The use of vetiver grass (Vetiveria zizanioides) in the
phytoremediation of soils contaminated with heavy metals. Appl. Geochem. 19: 1553–1565.
272 ETHNOBOTANY: Local Knowledge and Traditions
Chomchalow, N. and Hicks, P.A. 2001. Health Potential of Thai Traditional Beverages. Paper presented
at the 34th AISFT Annual Convention 2001, Adelaide, Australia, 1–4 July 2001; also published
in AU J.T. 5: 20–30.
Chomchalowm, N. 2002. Review and Update of the Vetiver System R&D in Thailand. Proc.
Chopra, R.N., Nayar, S., Chopra, I.C. 1956. Glossary of Indian medicinal plants, NISCAIR, 1st edition
1956: 254.
Chou, S.T., Lai, C.P. Lince and Shin, Y. 2012. Study of the Chemical composition, antioxidant activity
and anti-inflammatory activity of essential oils from Vetiveria zizanoides (L.) Nash. Food
Chemistry 134: 262–268.
Clark, L.G. and Fisher, J.B. 1987. Vegetative morphology of grasses: shoots and roots. pp. 37–45.
In: Soderstrom, T.R. (ed.). Grass Systematics and Evolution. Smithsonian Institution Press,
Washington.
Council of Scientific and Industrial Research (CSIR). 1976. Vetiveria. pp. 451–457. In: The Wealth of
India, Vol. X. Publications & Information Directorate, CSIR, New Delhi.
Cupp, M. 1999. Herbal remedies: Adverse effects and drug interaction. Ann. Fam. Physician 59:
1239–1244.
Dalziel, J.M. 1937. Useful Plants of West Tropical Africa. Crown Agents for the Colonies, London.
Dashora, K. and Gosavi, K.V. 2013. Grasses: An underestimated medicinal repository. Journal of
Medicinal Plant Studies 1(3): 151–157.
DeSmet. 2002. Herbal remedies. New Engl. J. Med. 347: 2046–2056.
Dikshit, A. and Husain, A. 1984. Antifungal action of some essential oil against animal pathogens.
Fitoterapia 55: 171–176.
Dubey, N.K. and Tripathi, P. 2004. Global promotion of herbal medicine: India’s opportunity. Curr.
Sci. 86: 37–41.
Elatler, E. and McCann, C. 1928. Revision of the flora of the Bombay Presidency. Gramineae. Journal
of the Bombay Natural History Society 32: 408–410.
Gogte, V.M. 2000. Ayurvedic pharmacology and therapeutic uses of medicinal plants, 1st ed., Mumbai:
Bharatiya vidya Bhavana 2000: 319–320 pp.
Gould, F.W. and Clark, C.A. 1983. Grass Systematics. 2nd edition. Texas A&M University Press,
College Station, Texas.
Greenfield, J.C. 1987. Vetiver Grass (Vetiveria zizanioides). A Method of Soil and Moisture Conservation.
1st ed. The World Bank, New Delhi.
Greenfield, J.C. 1988. Vetiver Grass (Vetiveria zizanioides). A Method of Soil and Moisture Conservation.
2nd ed. The World Bank, New Delhi.
Greenfield, J.C. 1989. Novel grass provides hedge against erosion. VITA News: 2014–15 Greenfield,
J.C. 1989. Vetiver Grass (Vetiveria spp.): The Ideal Plant for Vegetative Soil and Moisture
Conservation. Asia Technical Department, Agriculture Division, The World Bank, Washington.
Greenfield, J.C. 2002. Vetiver Grass: An essential grass for conservation of planet earth. Haverford,
PA: Infinity Publishing Co. [Google Scholar]
Han Xuesheng and Tory, L. Parker. 2017. Biological Activity of Vetiver (Vetiveria zizanioides)
essential oil in human dermal fibroblasts Cogent medicine, 4 (http://dxdoi.org101086/233120
4x2017.1298176).
Hart, B., Cody, R. and Truong, P. Efficacy of vetiver grass in the hydroponic treatment of post septic
tank effluent. October 6–9, Guangzhou, China. Proc. Third Int. Vetiver Conf. (ICV-3).
Hoang, T.T.T., Tu, T.C.L. and Dao, P.Q. 2007. Progress and results of trials using vetiver for
phytoremediation of contaminated canal sludge around Ho Chi Minh City. Hanoi, Vietnam. Proc.
Vetiver Workshop, Vietnamese.
Hooker, J.D. 1975. Flora of British India. Bishen Singh Mahendra Pal Singh, Dehra Dun, India.
http://interscience.org.uk/index.php/archive/47-volume-7-issue-3-may-june-2017/221-phytochemical-
study-of-usheera-vetiveria-zizanioides-linn-nash.
http://www.bimbima.com.
http://www.easyayurveda.com.
http://www.tandfonline.com/doi/ref/10.1080/15226510902787302?scroll=top.
http://www.vetiver.org/TVN_refs.htm.
An Overview of Vetiveria zizanioides (Linn.) Nash (Poaceae) 273
Hyun-Jin Kim, Feng Chen, Xi Wang, Hau Vin Chung and Zhengyu Jin. 2005. Evaluation of antioxidant
activity of vetiver (Vetiveria zizanioides L.) Oil and identification of its antioxidant constituents.
J. Agric. Food Chem. 53(2): 7691–7695.
Jain, S.K. 1991. Dictionary of Indian Folk Medicine and Ethnobotany. Deep Publ., New Delhi, India.
Joseph, J.K., Haridasan, A., Akhildev, K. and Pradeep Kumar, A.P. 2017. Applications of vetiver grass
(Chrysopagon zizanioides) in Ecosystem based disaster risk reduction studies from Kerala state
of India. J. Geogr. Nat. Disast. 7: 192, doi: 10.4172/2167-0587.1000192.
Juliard, C. 2001. Manuscript of Vetiverim 16. In Letters to the Editor, Vetiverim 17: 15.
Kaikade, R.S. and Ingole, S.N. 2014. Study of Anatomical and Phytochemical Biomarkers of Some
Medicinal Plants mentioned in Atharvaveda, Ph.D. Thesis submiteed to S.G.B. Amravati
University, Amravati.
Kam, A.J. and Alagesaboopathi, C. 2009. Ethnomedicinal plants and their utilization by villagers
in Kumaragiri Hills of Salem District of Tamil Nadu, India. African Journal of Traditional,
Complementary and Alternative Medicines 6(3): 222–227.
Kamboj, V.P. 2000. Herbal Medicine. Curr. Sci. 78(1): 35–39.
Khesorn Nanachit, Manasnant Bunchoo, Banyong Khantava and Chantana Khamvan. 2010.
Antimicrobial activity of roots of Vetiveria zizanoides (L.) Nash. Thai Pharmaceutical and Health
Science Journal 5(2): 99–1026.
Kirtany, J.K. and Paknikan, S.K. 1971. North Indian vetiver oils: comments on chemical composition
and botanical origin. Science and Culture 37: 395–396.
Kirtikar and Basu. 2000. Indian medicinal plants, 3rd ed., Delhi: Sri Satguru publications, 3699 pp.
Kokate, C.K., Purohit, A.P., Gokhale, S.B. and Furia, D.K. 1998. Pharmacognosy. 10th Edition, Nirali
Publication, Pune, pp. 319–320.
Liu, P., Zheng, C., Lin, Y., Luo, F., Lu, X. and Yu, D. 2003. Dynamic State of Nutrient Contents of
Vetiver Grass. Proc. Third International Vetiver Conf. China, October 2003.
Mabberley, D.J. 1989. The Plant-book: A portable dictionary of the higher plants. Reprinted with
corrections, Cambridge University Press, Cambridge.
Maistrello, L. and Henderson, G. 2001. Vetiver grass: Useful tools against Formosansubterranean
termites. Vetiverim 16: 8.
Manzoor-i-Khuda, M., Faruq, M.O., Rahman, M., Yusuf, M., Wahab, M.A. and Chowdhury, J. 1984.
Studies on the essential oil bearing plants of Bangladesh. Part 1. A preliminary survey of some
indigenous varieties. Bangladesh Journal of Scientific and Industrial Research 19(1-4): 151–169.
Martinez, J., Rosa, P.T.V., Menut, C., Leydet, A., Brat, P., Pallet, D. and Meireles, M.A.A. 2004. J.
Agr. Food Chem. 52: 6578–6584.
Mishra Snigdha, Sharma Satish, Kumar Mohapatra Sharmistha and Chauhan Deepa. 2013. An overview
on Vetiveria zizanioides. Research Journal of Pharmaceutical, Biological and Chemical Sciences
4(3): 777–783.
Murti, K.S. and Moosad, C.R. 1949. South Indian vetiver root study. American Perfume and Essential
Oil Record 54: 113–115.
Nair, E.V.G., Channamma, N.P. and Kumari, R.P. 1982. Review of the work done on vetiver (Vetiveria
zizanioides Linn.) at the Lemongrass Research Station, Odakkali. pp. 427–430. In: Atal, C.K. and
Kapur, B.M. (eds.). Cultivation and Utilization of Aromatic Plants. Regional Research Laboratory,
Council of Scientific and Industrial Research, Jammu-Tawi, India.
Nanachit Khesorn, Manasnant Bunchou, Banyong Khantava and Chantava Khamuan. 2010. Antimicrobial
activity of alkaloids from roots of Vetiveria zizanoides (L.) Nash. Thai Pharmaceutical and Health
Science Journal 5(2): 99–1026.
National Research Council. 1993. Vetiver Grass: A Thin Green Line Against Erosion. National Academy
Press, Washington.
National Resource Council. 1995. Vetiver Grass: A Thin Green Line Against Erosion. Washington,
DC: National Academy Press.
Pareek Archana and Ashwani Kumar. 2013. Ethnobotanical and Pharmaceutical Uses of Vetiveria
zizanoides (Linn) Nash: A medicinal plant of Rajasthan. International Journal of Life Sciences
and Pharma Research 3(4): 1–12.
274 ETHNOBOTANY: Local Knowledge and Traditions
Pichai, N.M.R., Samjiamjiaras, R. and Thammanoon, H. 2001. The wonders of a grass, Vetiver and its
multifold applications. Asian Infrastruct. Res. Rev. 3: 1–4.
Rao Srinivasa, G.M., Narasimha Rao and Prayaga Murthy. 2016. Diversity and indigenous uses of some
ethnomedicinal plants in papikondalu wildlife sanctuary, Eastern Ghats of Andhra Pradesh, India.
American Journal of Ethnomedicine 3(2): 6–10.
Sastry, K.N.R. 1998. Socio-economic dimensions of vetiver in rainfed areas of Karnataka, India. Proc.
ICV-1, Chiang Rai, Thailand, 243–248.
Sellar, W. 1992. The Directory of Essential Oils. C.W. Daniel Co Ltd., Great Britain.
Sethi, K.L., Chandra, V. and Singh, A. 1976. Adaptability of vetiver hybrid clones to saline-alkali soils.
pp. 166–169. In: Proceedings of Second Workshop on Medicinal and Aromatic Plants. Gujarat
Agricultural University, Anand, India.
Singh, G., Singh, B.S. and Kumar, B.R. 1978. Antimicrobial activity of essential oils against
keratinophilic fungi. Indian Drugs 16(2): 43–45.
Singh, K.K. and Maheshwari, J.K. 1983. Traditional phytotherapy amongst the tribals of Varanasi
district, U.P.J. Econ.Tax. Bot. 4: 829–838.
Singh, B. and Sankhala, K.S. 1957. From khas roots to rooh khas. Indian Forester 83(5): 302–306.
Smyle, J.W. and Magrath, W.B. 1990. Vetiver grass—a hedge against erosion. Paper presented at the
annual meeting of the American Society of Agronomy, October 2, 1990, San Antonio, Texas.
Thakur, R.S., Puri, H.S. and Akhtar, H. 1989. Major medicinal plants of India. pp. 521–527, CIMAP,
Lucknow, India.
Truong, P. 2002.Vetiver grass technology. pp. 114–132. In: Maffei, M. (ed.). Vetiveria. The Genus
Vetiveria, London and New York: Taylor and Francis Publishers.
Truong, P. and Smeal, C. 2003. Research, Development and Implementation of Vetiver System for
Wastewater Treatment: GELITA Australia. Pacific Rim Vetiver Network Tech. Bull. 3.
Virmani, O.P. and Data, S.C. 1975. Vetiveria zizanioides (Linn.) Nash. Indian Perfumer 19: 35–73.
Watson, L. and Dallwitz, M.J. 1988. Grass Genera of the World (with microfiche and data disks).
Australian National University Printing Service, Canberra.
WHO. 2000. General guidelines for methodology on research and evaluation of traditional medicines,
World Health Organization, Geneva.
World Bank. 1993. Vetiver Grass: The Hedge Against Erosion. 4th ed. The World Bank, Washington.
CHAPTER 14
Introduction
Some plants produce beneficial pharmacologic effects on the human body and have
been used for treating illnesses since the dawn of time. The therapeutic properties
are due to the secondary metabolites that naturally synthesize and accumulate
in these plants like alkaloids, sterols, terpenes, flavonoids, saponins, glycosides,
cyanogenic, tannins, resins, lactones, quiniles, volatile oils, etc. (Motaleb 2011).
These compounds are identified by the rigor of scientific, pharmacological,
toxicological and clinical tests in search of active ingredients that explain the
rational therapeutic use of these plants and promote the validity of its use (Muñoz
et al. 1999).
1
Facultad de Agronomía, Pontificia Universidad Católica de Chile.
2
Facultad de Química y Biología, Universidad de Santiago de Chile.
3
Centro de MicroBioinnovación, Facultad de Farmacia, Universidad de Valparaíso.
4
Centro Regional de Estudios en Alimentos Saludables (CREAS).
5
Facultad de Ciencias, Universidad de Santiago de Chile.
6
Vicerrectoría de Investigación, Desarrollo e Innovación, Universidad de Santiago de Chile.
† In memoriam
* Corresponding author: [email protected]
276 ETHNOBOTANY: Local Knowledge and Traditions
Peumus boldus, Salix chilensis, Solanum ligustrinum and Maytenus boaria to treat
internal, dental, rheumatic or menstrual pain, as well as neuralgia or headache;
Lysimachia serrulana, Salix chilensis and Sphacele salviae to treat paralysis;
Artemisia copa and Baccharis linearis (Ruiz & Pav.) Pers. (it is synonym of Baccharis
rosmarinifolia Hook. & Arn.) to treat convulsions; Chenopodium ambrosioides and
Salix chilensis for intestinal cramps; Latua pubiflora with narcotic activity; Geum
quellyon and Senecio eriophyton to treat impotence or contribute to the erection;
Senecio eriophyton and Chenopodium ambrosioides as stimulant or for fatigue
treatment; Senecio eriophyton as aphrodisiac and to chills (Fig. 14.1, Table 14.1).
Some adverse effects (toxic, carcinogenic and respiratory) were reported for
Chenopodium ambrosioides, Laurelia sempervirens and Solanum ligustrinum
(Muñoz et al. 1999).
On the other hand, 12 of the 30 species were studied for their pharmacological
action (Acaena magellanica, Aristotelia chilensis, Artemisia copa, Buddleja
globosa, Chenopodium ambrosioides, Fabiana imbricata, Haplopappus baylahuen,
Latua pubiflora, Laurelia sempervirens, Peumus boldus, Proustia pyrifolia and
Ugni molinae), and another twelve were studied chemically (Araucaria araucana,
Azara microphylla, Centaurium cachanlahuen, Geum quellyon, Lampayo officinalis,
Maytenus boaria, Parastrephia lepidophylla, Quillaja saponaria, Salix chilensis,
Senecio eriophyton, Solanum ligustrinum and Sphacele alviae). Finally, no scientific
studies were found for 6 of these species (Baccharis rosmarinifolia, Cryptantha
hispida, Lysimachia sertulata, Oenothera acaulis, Sophora macnabiana and
Wahlenbergia linarioides).
Native plants with different
pharmacological effects
Nerve disorders
Analgesic
Sedative
Intemal pain
Paralysis treatment
Anticonvulsant
Intestinal cramps
Narcotic activity
Importence
Fatigue
Aphrodisiac
With adverse effects
Fig. 14.1. Pharmacological uses and effects associated with Chilean medicinal plants. The pie chart
highlights the use in nervous disorders and the analgesic and sedative properties.
Table 14.1. Scientific name, traditional medicinal applications, used parts, mode of administration, experimental scientific studies and reference used and scientific
studies of the medicinal plants with report of use for treatment of diseases of nervous origin.
Scientific Name Traditional Medicinal Used Parts Mode of Experimental Scientific Reference Used And
Applications Administration Studies Scientific Studies
1 Acaena magellanica Analgesic Whole plant Infusion A 20% w/v infusion administered orally at 16 Feresin et al. (2002)
(LAM.) VAHL mL/kg presented analgesic effect in the acetic
acid-induced abdominal constriction test in
mice.
2 Araucaria araucana Headache Resin Patches Five diterpenes were isolated from this plant, Muñoz et al. (1999)
(Molina) K. Koch,* but its biological function is not known enough.
3 Aristotelia chilensis Analgesic activity Leaves Infusion Leaves have alkaloids and tannins which act Muñoz et al. (1999),
(Molina) Stuntz* as analgesics. In several topical analgesia (2011), Misle et al.
models, dichloromethane, methanol, aqueous (2011)
extract and a crude mixture of alkaloids were
active in the formalin assay. In tail flick test,
a crude mixture of alkaloids and methanol
extract were the most active (58.2% and 55.2%,
respectively). In the tail formalin assay, the
methanol extract (74.1%) was the most active.
4 Artemisia copa Phil* Sedative, anxiolytic and Aerial parts Infusion At doses up to 1.5 g/kg, a dose-dependent sleep Miño et al. (2010)
278 ETHNOBOTANY: Local Knowledge and Traditions
Scientific Name Traditional Medicinal Used Parts Mode of Experimental Scientific Reference Used And
Applications Administration Studies Scientific Studies
9 Chenopodium Stimulating, analgesic Root Infusion It contains thiamine, riboflavin, niacin, Muñoz et al. (1999),
ambrosioides L. and antispasmodic vitamin C, ascaridol, geranidol, 1-limonene, Ibironke and Ajiboye
myrcene, p-cymene, d-alcamphor, butactic (2007)
acid, spinasterol, terpinene, long chain alkyls,
methyl salicylate, alkaloids, saponins and various
glycosides. Analgesic effect was observed with
the hotplate device maintained at 55°C as well as
on the early and late phases of formalin-induced
paw licking in rats. The 10% infusion has mild
antispasmodic activity in rats. Infusions may be
toxic (DL50 > 1.0 g/kg in mice).
10 Cryptantha hispida Falling Asleep - - No studies found. Mellado et al. (1996)
(Phil.) Reiche*
11 Fabiana imbricata Sedative and analgesic Bark and logs Infusion Derivatives of anthraquinones, terpene Muñoz et al. (1999)
Ruiz and Pavon* alkaloids, sugars and flavonoids have been
isolated of this plant. The hydroalcoholic
extract showed analgesic effects.
280 ETHNOBOTANY: Local Knowledge and Traditions
12 Geum quellyon Impotence Root Decoction It was detected that it contains hydrolyzable Muñoz et al. (1999)
Sweet* tannins, flavonoids, gallic acid and eugenol, but
there is no biological-chemical information that
supports its medicinal use.
13 Haplopappus Aphrodisiac and chills Leaves and Infusion or Anthraquinone glycosides, preniletine and Muñoz et al. (1999)
baylahuen treatment stems decoction flavonoids have been isolated from the aerial
J.Remy* parts and stems. Some animal tests showed that
the infusion of the plant has relaxing effects on
the uterus.
14 Lampayo officinalis it produces sleep Leaves Infusion Extract showed higher concentrations of Mellado et al. (1996),
F. Phil. ex Murillo* phenols and flavonoids. Garrido et al. (2013),
Morales and Paredes
(2014)
15 Latua pubiflora Narcotic, anxiolytic and Leaves and Infusion It contains alkaloids. The anxiolytic effect of an Plowman et al.
(Griseb.) Baill.* sedative activities flowers alkaloid fraction was corroborated. The alkaloid (1971), Rojas (2002),
extract has sedative and anxiolytic properties Muñoz and Casale
involving the GABAA receptor. The non- (2003), Ulloa (2004)
alkaloid extract presents a sedative property not
associated with GABAA.
16 Laurelia Headache Leaves Infusion It contains complex alkaloids of aporphine Muñoz et al. (1999),
sempervirens type and bisbenzylisoquinolyl, and safrole. I.V. Schmeda-Hirschmann
(Ruiz and Pav.) Tul* administration of a hydroalcoholic extract to et al. (1994)
rats elicited a hypotensive response of (–27.0%)
in blood pressure of normotensive animals at a
dose of 5 mg crude extract. Carcinogenic effects
have been detected in experimental animals due
to the use of the essential oil of the leaves (high
safrole 91%).
17 Lysimachia sertulata Paralysis - - No studies found. Mellado et al. (1996)
Baud*
18 Maytenus boaria Dental and internal Leaves and Infusion A variety of sesquiterpenes, triterpenes, Muñoz et al. (1999)
Molina analgesic seeds or decoction polyphenols and flavonoids have been
isolated from the aerial. Sesquiterpenes are
antiinflammatory and polyphenols are effective
antioxidant in association with proteins and
amino acids normalizing the cardiovascular
function.
19 Oenothera acaulis Antidepressant and - - No studies found. Mellado et al. (1996)
Cav* analgesic
Chilean Medicinal Plants Used for Nervous System Ailments
Scientific Name Traditional Medicinal Used Parts Mode of Experimental Scientific Reference Used And
Applications Administration Studies Scientific Studies
20 Parastrephia Analgesic Leaves and Infusion Two benzofurans (tremetone 1 and Benites et al. (2012),
lepidophylla (Wedd.) branches methoxytremetone 6) were isolated. Tremetone Hierba medicinal
Cabrera 1 exhibited a morphine-like analgesic property. (2016)
21 Peumus boldus Sedative, antineuralgic Leaves Infusion and The essential oil contains terpene hydrocarbons, Muñoz et al. (1999)
Molina* and antirheumatic cataplasma common flavonol glycosides, aporophinoid
alkaloids and non-aporphinoid alkaloids.
The wood contains laurolitsina and several
unidentified bases. The bark has boldine,
benzylisoquinolinic alkaloids and coclaurine.
Boldine exerts in vitro relaxing effect on
rat musculature, directly interfering with
the cholinergic mechanism involved.
Antiinflammatory activity of ethanolic extracts
has also been demonstrated.
22 Proustia pyrifolia DC Analgesic Leaves and Infusion and The evaluation of the topic antiinflammatory Delporte et al. (2005),
roots showers activities induced by arachidonic acid, and Tesauro Regional
phorbol 12-myristate 13-acetate of the different Patrimonial (2016b)
282 ETHNOBOTANY: Local Knowledge and Traditions
Scientific Name Traditional Medicinal Used Parts Mode of Experimental Scientific Reference Used And
Applications Administration Studies Scientific Studies
28 Sphacele salvia Paralysis treatment Leaves Infusion and In this plant were found abetes and ursolic acid Mellado et al. (1996),
(Lindl). Briq.* tonic as main secondary metabolites. Also, camosol Flagg (2000), Escuder
and rosmadial were found. Antitumorigenic et al. (2002)
activity in oncology screens and antioxidant
activity have been documented.
29 Ugni molinae Turcz.* Analgesic Leaves Infusion Dichloromethane (DCM), ethyl acetate Delporte et al. (2007)
(EA) and methanol (ME) leaf extracts were
assessed in mice showing a dose-dependent
antinociceptive activity in all the assays under
different administration routes.
30 Wahlenbergia Sedative Leaves and Infusion No studies found. Mellado et al. (1996),
linarioides Schrad. wood Montes et al. (1974)
ex Roth
*endemic
284 ETHNOBOTANY: Local Knowledge and Traditions
Chilean Medicinal Plants Used for Nervous System Ailments 285
References
Arrau, S., Delporte, C., Cartagena, C., Rodríguez-díaz, M., González, P., Silva, X., Cassels, B.K. and
Miranda H.F. 2011. Antinociceptive activity of Quillaja saponaria Mol. saponin extract, quillaic
acid and derivatives in mice. J. Ethnopharmacol 133(1): 164–167. http://doi.org/10.1016/j.
jep.2010.09.016.
Backhouse, N., Delporte, C., Apablaza, C., Farías, M., Goïty, L., Arrau, S., Negrete, R., Castro, C. and
Miranda, H. (2008a). Antinociceptive activity of Buddleja globosa (matico) in several models of
pain. J. Ethnopharmacol. 119(1): 160–165. http://doi.org: 10.1016/j.jep.2008.06.022.
Backhouse, N., Rosales, L., Apablaza, C., Goïty, L., Erazo, S., Negrete, R., Theodoluz, C., Rodríguez,
J. and Delporte, C. 2008b. Analgesic, anti-inflammatory and antioxidant properties of
Buddleja globosa, Buddlejaceae. J. Ethnopharmacol. 116(2): 263–269. http://doi.org: 10.1016/j.
jep.2007.11.025.
Benites, J., Gutierrez, E., López, J., Rojas, M., Rojo, L., Costa, M.C., Vinardell, M.P. and Buc Calderon,
P. 2012. Evaluation of analgesic activities of tremetone derivatives isolated from the Chilean
altiplano medicine Parastrephia lepidophylla. Nat. Prod. Commun. 7(5): 611–4.
286 ETHNOBOTANY: Local Knowledge and Traditions
Delporte, C., Backhouse, N., Erazo, S., Negrete, R., Vidal, P. and Silva, X. 2005. Analgesic-
antiinflammatory properties of Proustia pyrifolia. J. Ethnopharmacol. 99: 119–124. http://doi.
org/10.1016/j.jep.2005.02.012.
Delporte, C., Backhouse, N., Inostroza, V. and Aguirre, M.C. 2007. Analgesic activity of Ugni molinae
(murtilla) in mice models of acute pain. J. Ethnopharmacol. 112: 162–165. http://doi.org/10.1016/j.
jep.2007.02.018.
Escuder, B., Torres, R., Lissi, E., Labbé, C. and Faini, F. 2002. Antioxidant capacity of abietanes from
Sphacele salviae. Nat. Prod. Lett. 16(4): 277–281. http://.org/10.1080/10575630290020631.
Estomba, D., Ladio, A. and Lozada, M. 2006. Medicinal wild plant knowledge and gathering patterns
in a Mapuche community from North-western Patagonia. J. Ethnopharmacol. 103(1): 109–119.
doi:10.1016/j.jep.2005.07.015.
Feresin, G.E., Schmeda-hirschmann, G., Feresin, G.E., Tapia, A., R., A.G., Delporte, C., … Schmeda-
hirschmann, G. 2002. Free radical scavengers, anti-inflammatory and analgesic activity of Acaena
magellanica analgesic activity of Acaena magellanica. J. Phar. Pharmacol. 54: 835–844. http://
doi.org/10.1211/0022357021779014.
Flagg, M.L. 2000. Bioprospecting, chemical investigations and drug discovery from Chilean plants.
(Unpublished Ph.D degree thesis). University of Arizona, Tucson, E.E.U.U. Retrieved from http://
arizona.openrepository.com/arizona/bitstream/10150/284167/1/azu_td_9972115_sip1_m.pdf.
Garrido, G., Ortiz, M. and Pozo, P. 2013. Fenoles y flavonoides totales y actividad antioxidante de
extractos de hojas de Lampaya medicinalis F. Phil. J. Pharm. Pharmacogn Res. 1(1): 30–38.
Hierba Medicinal. 2016. Thola para la tos y expectorar en resfriados y gripes. Retrieved from http://
www.hierbamedicinal.es/thola-para-la-tos-y-expectorar-en-resfriados-y-gripes.
Houghton, P.J. and Manby, J. 1985. Medicinal plants of the Mapuche. J. Ethnopharmacol.
13(1): 89–103. http://doi:10.1177/1533210110391077.
Ibironke, G.F. and Ajiboye, K.I. 2007. Studies on the anti-inflammatory and analgesic properties of
Chenopodium ambrosioides leaf extract in rats. Int. J. Pharmacol. 3(1): 111–115. http://doi.
org/10.3923/ijp.2007.111.115.
Mellado, V., Medina, E. and San Martín, C. 1996. Herbolaria médica de Chile, diagnóstico de su estado
actual y perspectivas futuras para la medicina oficial chilena. Santiago, Chile: Ministerio de Salud.
Miño, J.H., Moscatelli, V., Acevedo, C. and Ferraro, G. 2010. Psychopharmacological effects of
Artemisia copa aqueous extract in mice. Pharm. Biol. 48: 1392–1396. http://doi.org/10.3109/1
3880209.2010.486407.
MINSAL (Ministerio de Salud). 2009. Medicamentos herbarios tradicionales. Retrieved from http://
www.minsal.cl/portal/url/item/7d9a8480e0821613e04001011e01021b.pdf.
Misle, E., Garrido, E., Contardo, H. and González, W. 2011. Maqui [Aristotelia chilensis (Mol.)
Stuntz]—the Amazing Chilean Tree: a review.
Montes, M., Wilkomirsky, T. and Ubilla, H. 1974. Quelques aspects de la medication vegetale populaire
dans la region de Concepcion (Chili). Planta Medica 25(02): 183–192.
Morales, G. and Paredes, A. 2014. Antioxidant activities of Lampaya medicinalis extracts and their
main chemical constituents. BMC Complem. Altern. M. 14(1): 1. http://doi.org/: 10.1186/1472-
6882-14-259.
Moreira-Muñoz, A. 2011. Plant Geography of Chile. (Plant and Vegetation, Volume 5). London, New
York: Springer.
Motaleb, M.A. 2011. Selected Medicinal plants of chittagong hill tracts. Retrieved from http://cmsdata.
iucn.org/downloads/medicinal_plant_11_book.pdf.
Muñoz, O., Montes, M. and Wilkomirsky, T. 1999. Plantas medicinales de uso en Chile: química y
farmacología. (2da ed.) Santiago, Chile: Editorial Universitaria S.A.
Muñoz, O. and Casale, J.F. 2003. Tropane alkaloids from Latua pubiflora. Zeitschrift für Naturforschung
C, 58(9-10): 626–628. http://doi.orh/doi: 10.1515/znc-2003-9-1003.
Muñoz, O., Christend, P., Crettond, S., Backhouse, N., Torres, V., Correa, O., Costa, E., Miranda, H. and
Delporte, C. 2011. Chemical study and anti-inflammatory, analgesic and antioxidant activities of
the leaves of Aristotelia chilensis (Mol.) Stuntz, Elaeocarpaceae. J. Phar. Pharmacol. 63: 849–859.
http://doi.org/10.1111/j.2042-7158.2011.01280.x.
Chilean Medicinal Plants Used for Nervous System Ailments 287
Niemeyer, H.M. 1995. Biologically active compounds from Chilean medicinal plants. pp. 137–153.
In: Arnason, J.T., Mata, M. and Romeo, J.T. (eds.). Phytochemistry of Medicinal Plants (Volume
29). Nueva York: Plenum Press.
Plowman, T., Gyllenhaal, L.O. and Lindgren, J.E. 1971. Latua pubiflora magic plant from Southern
Chile. Bot. Mus. Leafl. 23(2): 61–92. Retrieved from http://www.jstor.org/stable/41762272.
Rahimi, R., Ghiasi, S., Azimi, H., Fakhari, S. and Abdollahi, M. 2010. A review of the herbal
phosphodiesterase inhibitors; future perspective of new drugs. Cytokine 49(2): 123–129. http://
doi.org doi: 10.1016/j.cyto.2009.11.005.
Rojas, M.A. 2002. Caracterización química de extractos de “palo brujo” (Latua pubiflora (Griseb.) Phil.),
con propiedades depresoras del sistema nervioso central, y su caracterización farmacológica en
ratones. (Unpublished Thesis for the title of pharmaceutical chemist). Universidad Austral de Chile,
Valdivia, Chile. Retrieved from http://cybertesis.uach.cl/tesis/uach/2002/fcr741c/doc/fcr741c.pdf.
Sagareishvili, T.G., Alaniya, M.D. and Kemertelidze, É.P. 1983. A new flavonol glycoside from Azara
microphylla. Chem. Nat. Compd. 19(3): 275–278. http://doi.org:10.1007/BF00579757.
Schmeda-Hirschmann, G., Loyola, J., I. and Rodriguez, J. 1994. Hypotensive effect of Laurelia
semperviren (Monimiaceae) on normotensive rats. Phytother. Res. 8: 49–51. http://doi.org/10.1002/
ptr.2650080112.
Singh, S., Ali, A., Singh, R. and Kaur, R. 2016. Sexual Abnormalities in Males and Their Herbal
Therapeutic Aspects. Pharmacologia, 1–11. http://doi.org/10.5567/pharmacologia.2013.265.275.
Tesauro Regional Patrimonial. 2016a. Azara microphylla, corcolén. Retrieved from http://www.
tesauroregional.cl/trp/tesauro/default.asp?a=338&Element_ID=2212.
Tesauro Regional Patrimonial. 2016b. Proustia pyrifolia, tola blanca Retrieved from http://www.
tesauroregional.cl/trp/tesauro/default.asp?a=338&Element_ID=2079.
Tesauro Regional Patrimonial. 2016c. Quillaja saponaria, quillay. Retrieved from http://www.
tesauroregional.cl/trp/tesauro/default.asp?a=338&Element_ID=2288.
Tesauro Regional Patrimonial. 2016d. Senecio eriophyton, chachacoma. Retrieved from http://www.
tesauroregional.cl/trp/tesauro/default.asp?a=338&Element_ID=2057.
Ulloa, G.E. 2004. Estudio químico de un extracto alcaloideo de Latua pubiflora (Griseb) (Latúa) y
evaluación farmacológica de los compuestos alcaloideos (Unpublished Thesis for the title of
pharmaceutical chemist). Universidad Austral de Chile, Valdivia, Chile. Retrieved from http://
cybertesis.uach.cl/tesis/uach/2004/fcu.42e/pdf/fcu.42e-TH.4.pdf.
Waizel-Bucay, J. 2011. Plantas y compuestos importantes para la medicina: los sauces, los salicilatos
y la aspirina. Rev. Fitoter 61–75.
CHAPTER 15
Introduction
Traditional knowledge on the use of medicinal plants to treat human diseases
still exists in many parts of the globe (Katewa et al. 2004, Mahishi et al. 2005).
Safe, effective and inexpensive indigenous remedies are gaining popularity and
communities in Nepal are still practicing the use of medicinal plants to treat a
variety of ailments (Chaudhary 1998, Bhattarai 2009, Manandhar 2002, Baral
and Kurmi 2006). Tharus are a culturally and linguistically diverse ethnic group
of Nepal Tarai having a long history of knowledge on the use of medicinal plants.
In the rural areas of Tharu communities, even today healthcare among the
Tharus is checked by the local Gurewa (traditional healer), who performs primeval
rites of protection, blessings and healing by using local medicinal herbs (Manandhar
2002). Tharu people mainly settled in Surkhet, Dang, Kailali, Kanchanpur, Banke,
Kapilvastu, Rupandehi, Nawalparasi, Chitwan, Parsa, Bara, Rautahat, Sindhuli,
Udyapur, Morang and Jhapa districts in Nepal (Fig. 15.1).
The fertile land of Tarai is called rice basket of Nepal (Sapkota 2014,
Bhattachan 2016). Tharu people live in villages in houses plastered with mud and
cow dung (Pyakuryal 1982). The houses are large and communal (Meyer and Deuel
1999). The Tharus are recognized as an official nationality by the Government of
Nepal (Lewis et al. 2014), whereas the Government of India recognizes the Tharu
people as a scheduled tribe (Verma 2010).
Fig. 15.1. Districts showing the main settlements by the Tharu communities in Nepal.
who works for the village welfare and also manages the cultural traditions. Tharus
have Mongoloid features with dark and semi-dark colors, and are believed to have
come to Nepal from India during the Muslim invasion in 12th and 13th century
(Pyakuryal 1982, Gurung 1996). They are rich in culture, traditions, rites and rituals.
In 1854, the Mulkiain categorized Nepal’s legal system and divided society into
a system of castes. Tharus were placed between the touchable and untouchables
social hierarchy (Muller-Boker 1999a,b, McDonaugh 1999, Gurung 1996).
Even when the Tarai was avoided by others communities because of the
influence of malaria, only the Tharus managed to live there (Pyakuryal 1982,
Manandhar 2002, Gurung 1996). Their illiteracy and lack of representation in
government made it difficult for them to struggle against the new landlords
(Pyakuryal 1982). Many fell into debt and were forced to become bonded laborers-
Kamaiyas (men) and Kamlaharis (women) (McDonaugh 1999, Patterson 1982,
Gurung 1996). Tharus also celebrate Hindu festivals. Each of the Tharu family
worships its personal tutelary deity who is represented by a lump of earth mixed
with multi-colour cotton threads, crude sugarcane and a gold coin in the centre
(Pyakuryal 1982, Muller-Boker 1999a,b).
Fig. 15.3. Tharu men knitting fishing net and carrying Bauhinia vahlii leaves.
the aastami-8th days of Dashain). During jitiya, Mothers keep fasting even without
drinking a drop of water with full dedication and faith for the long life and well-
being of her son. The fasting completes after ten days from the sunrise (Pyakuryal
1982). In this day, Tharu women perform their traditional dance in the various
programs. Tharu people also celebrate Dashain wearing new clothes and eating
delicious foods. It is celebrated for ten days which falls after two days of jitiya.
Chhath is another important festival. On this day, people worship the sun and
keep fasting without drinking a drop of water. Maghi is the most important festival
which is considered as the New Year for the Tharu community. People take bath
at the nearest water sources. On this day, delicious foods like sesame laddus, rice
pudding, fish and meat are made and served (Pyakuryal 1982). Fagu is another
important festival known as Holi in Nepal which is celebrated by sprinkling colors
on each other and singing songs (Pyakuryal 1982, Manandhar 2002). The author
has been working with the Tharu communities of Nepal since long time and has
gathered a rich knowledge of the Tharu cultures and traditions (Fig. 15.4).
Monogamous marriage system has been practiced among the Tharu people.
Traditionally, marriages were often arranged during the pregnancies of two women.
292 ETHNOBOTANY: Local Knowledge and Traditions
Fig. 15.4. Interaction with the local Tharu people about the medicinal plants in Bardiya.
Most Tharus now practice conventional arranged marriages and also practice love
marriages, inter caste marriage, marriage after courtship and eloping (Muller-Boker
1999a,b). The birth ceremony is celebrated at the age of five months for the girl
child and at the age of six-seven months for boys. On this day, rice pudding is eaten
by the child and the name of the baby is also kept. Most of the Tharu cremate their
deceased; others, however, bury them. There is a strange custom of keeping men
face down and women face up during the burial and the mourning period is about
thirteen days (Pyakuryal 1982).
Medicinal Plants
A total of 324 plant species belonging to 100 families used by the Tharu community
in Nepal were presented in this chapter (Table 15.1). The plant species were arranged
alphabetically according to scientific name, followed by family names, parts used,
Nepali and Tharu names, medicinal usage and reference citations (Table 15.1).
The top ten largest families are: Fabaceae (29 species), followed by Lamiaceae
(21 species), Asteraceae (18 species), Solanaceae (13), Poaceae, Euphorbiaceae
and Moraceae (11 species each), Malvaceae and Apocynaceae (10 species each)
and Cucurbitaceae (9 species) (Fig. 15.5).
Similarly, Amaranthaceae and Rubiaceae are represented by 7 species each
followed by Convolvulaceae and Cucurbitaceae (6 species each). Four families
Anacardiaceae, Boraginaceae, Myrtaceae and Zingiberaceae are represented by
5 species each (Table 15.2). Likewise, Acanthaceae, Combretaceae, Lythraceae,
Polygonaceae and Rutaceae were represented by 4 species each. Eleven families,
Amaryllidaceae, Annonaceae, Apiaceae, Cyperaceae, Dioscoraceae, Phyllanthaceae,
Plantaginaceae, Pteridaceae, Sapotaceae, Urticaceae and Verbenaceae were
represented by 3 species each. Twelve families, Bigioniaceae, Equisetaceae,
Lauraceae, Linaceae, Meliaceae, Nyctaginaceae, Orchidaceae, Oxalidaceae,
Table 15.1. Medicinal plants of Tharu communities of Nepal.
Plant’s Scientific Name (family name); Nepali and Tharu Medicinal Usage References
Parts Used names
Abelmoschus moschatus Moench. Bankapas Cuts, wounds Dangol and Gurung 1991
(Malvaceae); Rt
Abelmoscus esculentus (L.) Moench. Bhindi (N) Constipation Chapagain et al. 2004
(Malvaceae); Rt
Abrus precatorius L. (Fabaceae); Sd, Rt, Lvs Titihar, Chilahariyak Fever, stomach and eye diseases, asthma, Acharya and Acharya 2009,
thond (T) uterus problem, boils, cough, sore throat, Manandhar 2002, Chapagain et al.
headache, cold, blood purifier, malaria, 2004
paralysis, nerve diseases, skin diseases,
sciatica, rheumatism, asthma, dental caries,
urinary infection
Abutilon indicum (L.) St Sweet (Malvaceae); Baliyari (T) Body swellings, wounds, blisters, boils Dangol and Gurung 1991
Lvs
Acacia catechu (L.f.) Willd. (Fabaceae); St, Khayar (N) Diarrhea, dysentery, bodyache, blood Bhattarai et al. 2009, Chapagain et al.
Lvs, Sap accumulation, bone fracture, cough 2004, Manandhar 1985
Acacia nilotica (L.) Del. (Fabaceae); Br, Fl Babul Dysentery, diarrhea, quench thirst Dangol and Gurung 1991
Achyranthes aspera L. (Amaranthaceae); Rt, Naksirka, Uthaanna, Diarrhea, dysentery, constipation, blisters, Bhattarai et al. 2009, Chapagain et
Lvs, St, WP Ultakur (T) stomachache, headache, toothache, snake al. 2004, Manandhar 1985, 1988,
scorpion sting, delivery problems, vomiting, 1990, 1989a,b, Muller-Boker 1999a,
fever, fatigue, itchy skin, indigestion, dental Dangol and Gurung 1991, Mandar
trouble, bleeding, menstrual disorders and Chaudhary 1993
Achyranthes bidentata Blume Ultakur (T) Wounds, blisters Chapagain et al. 2004
(Amaranthaceae); WP
Acorus calamus L. (Acoraceae); Rt, Rh Bojho (N); Katara, Bajh Roundworm, hookworm cough, cold, sore Bhattarai et al. 2009, Acharya and
(T) throat, tonsillitis, bronchitis, anthelmintic Acharya 2009, Chapagain et al. 2004,
Dangol and Gurung 1991
Medicinal Plants Used by the Tharu Communities in Nepal
Adiantum caudatum L. (Pteridaceae); Sht Ratijari Fever Dangol and Gurung 1991
Ltx, Lvs Ghyukuwanr (T) skin irritations, fever, constipation, jaundice, 2004, Manandhar 2002
gonorrhea, kidney pains, indigestion, peptic
ulcers, cough, cold, dropsy
Alstonia scholaris (L.) R.Br. (Apocynaceae); Chhativan (N) Diarrhea, dysentery, bodyache, breast pain, Bhattarai et al. 2009, Chapagain et al.
Br, Ltx, WP tonic, fever, great thrist, menstrual disorders 2004, Muller-Boker 1999a, Mandar
and Chaudhary 1993
Alternanthera sessilis (L.) R.Br. ex DC. Saranchi, gantha phula, Fever, cough, cold, scabies, cuts, wounds, Taylor et al. 1996, Manandhar 1985,
(Amaranthaceae); WP, Aep, Rt garri (T) venereal diseases, dysuria, bloody dysentery, 2002, Mandar and Chaudhary 1993,
mental disorder, heat stroke Manandhar 1985
Amaranthus spinosus L. (Amaranthaceae); Setolode; Kattia maattia, Diuretic, cooling agent, constipation, fever, Bhattarai et al. 2009, Chapagain et al.
Rt, Lvs Kantiya, Makhan (N,T) diarrhea, dysentery, indigestion, vomiting, 2004, Manandhar 2002, Dangol and
gonorrhea, menorrhagia, boils, antidote Gurung 1991
Ananas comosus (L.) Merr. (Bromeliaceae); Anar (T) Arthritis/rheumatism Chapagain et al. 2004
Fr, Lvs
Annona reticulata L. (Annonaceae); Lvs, Fr Sarifa (N) Cuts, wounds, diabetes Mandar and Chaudhary 1993
Annona squamosa L. (Annonaceae); Lvs Sarifa (N) Boils Chapagain et al. 2004
Antidesma acidum Retz. (Phyllanthaceae); Dakhi, Dakhee (T) Snake scorpion sting, bone fracture Chapagain et al. 2004
Lvs, Fr, Br
Areca catechu L. (Arecaceae); Br Supari (N) Arthritis Mandar and Chaudhary 1993
Argemone mexicana L. (Papaveraceae); Fl, Bharbanda (T) Boils, eye complaints, itches Chapagain et al. 2004, Mandar and
St, Sd Chaudhary 1993
Artemisia indica Willd. (Asteraceae); Rt, Lvs Titepati (N); Pati (T) Gastritis, paralysis, scabies, anthelmintic, Bhattarai et al. 2009, Manandhar
ringworm 1985, 1994
Artemisia vulgaris L. (Asteraceae); WP Kurza Repellent for bugs, flcas Dangol and Gurung 1991
Artocarpus heterophyllus Lam. (Moraceae); Fr Kathar (N) Swelling part of scrotum Bhattarai et al. 2009
Artocarpus integer (Thunb.) Merr. Rukh katahar (N) Tuberculosis Chapagain et al. 2004
(Moraceae); Sd
Artocarpus lacucha Buch.-Ham. (Moraceae); Barhar Headache, constipation, diarrhea, dysentery Chapagain et al. 2004, Mandar and
WP, St, Br, Rt (N) Chaudhary 1993
Asparagus racemosus Willd. (Asparagaceae); Santapsatauri, Kurela Tonic in lactating a postpartum mother, Bhattarai et al. 2009, Chapagain et al.
Rt (T) anthelmintic, delivery, vomiting, burning 2004, Muller-Boker 1999a, Mandar
sensation in urination and Chaudhary 1993, Manandhar
1985
Asparagus racemosus Willd. var. subacerosus Santawar (T) Acharya and Acharya 2009
Baker (Asparagaceae); Rt
Azadirachta indica A. Juss. (Meliaceae); Lvs, Neem (N) Anthelmentic, fever, gastritis, stomachache, Bhattarai et al. 2009, Acharya and
Br cough, reduce sugar level, cooling agent, Acharya 2009, Chapagain et al. 2004,
diabetes, wounds, blisters, itches, skin Muller-Boker 1999a, Mandar and
diseases, tootache Chaudhary 1993
Bauhinia vahlii Wight and Arn. (Fabaceae); Bhorla (N); Malu, Pulmonary tuberculosis, abrasions, urinary Bhattarai et al. 2009, Chapagain et al.
Medicinal Plants Used by the Tharu Communities in Nepal
Berberis asiatica DC. (Berberidaceae); Rt Chutro (N) Boils Chapagain et al. 2004
Biophytum sensitivum (L.) DC. (Oxalidaceae); Lajmohani (T) Insomnia, fever Chapagain et al. 2004, Dangol and
WP Gurung 1991
Boehmeria platyphylla D.Don (Urticaceae); Khasreti (N) Cut, wounds Bhattarai et al. 2009, Manandhar 1985
Rt, Lvs
Boerhavia diffusa L. (Nyctaginaceae); WP Churchuriya (T) Headache Manandhar 1985
Bombax ceiba L. (Malvaceae); Ltx, Fr, Br, Rt, Simal; Simra (N, T) Diarrhea, urinary disorder, vaginal Bhattarai et al. 2009, Acharya and
Sht, Sap and intestinal bleeding, bone fracture, Acharya 2009, Chapagain et al. 2004,
constipation, wounds, cuts, blisters, worms, Muller-Boker 1999a, Manandhar
fever, dysentery, cough 1989a,b, 1990, Mandar and
Chaudhary 1993
Brucea javanica (L.) Merr. (Simaroubaceae); Bhakimlo (N) Diarrhea Chapagain et al. 2004
Fr
296 ETHNOBOTANY: Local Knowledge and Traditions
Butea monosperma (Lam.) Taub. Kuntz Parasin Appetizer, weakness Chapagain et al. 2004
(Fabaceae); Br (T)
Caesalpinia bonduc (L.) Roxb. (Fabaceae); Kathgarel Fever Mandar and Chaudhary 1993
Lvs, Bd
Caesulia axillaris Roxb. (Asteraceae); WP Gerguj (T) Wounds Muller-Boker 1999a
Calamus tenuis Roxb. (Arecaceae); Rt Bet (N) Delivery problems, menstrual problems, Chapagain et al. 2004
miscarriages
Callicarpa macrophylla Vahl. (Lamiaceae); St, Dahigola, Dahigona (T) Headache, diarrhea, wounds, blisters, Chapagain et al. 2004, Muller-Boker
Rt, Fr, Lvs fever, chickenpox, boils, rash, indigestion, 1999a, Manandhar 1980, 1987a,
rheumatic troubles, ear achc 1989b, 1990, Shrestha 1985, Dangol
and Gurung 1991
Calotropis gigantea (L.) Dryand. Aank (N); Madar, Yank Fractured bone, boils, gingivitis, sinusitis, Bhattarai et al. 2009, Acharya and
(Apocynaceae); (T) swelling of testes, body pain, pimples, Acharya 2009, Chapagain et al. 2004,
Ltx, Twg, Lvs, Fr, St headache, blood accumulation, body Manandhar 1985, 1990, 1986b, 2002,
swelling, cuts, delivery, wounds, alleviate Muller-Boker 1999a, Dangol and
pain, cough, sprain, whitlow, injurious to Gurung 1991
eye, hastening suppuration, arthritis
Calotropis procera (Aiton.) Dryand. Akon Diarrhea, dysentery Mandar and Chaudhary 1993
(Apocynaceae);
Br
Cannabis sativa L. (Cannabaceae); Sd, Fl, Lvs Gajha (N) Diarrhea, dysentery, Bhattarai et al. 2009, Chapagain et al.
constipation, cough, cold, cuts, indigestion 2004, Dangol and Gurung 1991
Careya arborea Roxb. (Lecythidaceae); Br, Fr Kumbhi (T) Wound, diarrhea, fever, snake bite, cuts Acharya and Acharya 2009,
Chapagain et al. 2004
Carica papaya L. (Caricaceae); Sd, Fr Mewa (N) Insecticidal, Jaundice Mandar and Chaudhary 1993
Carissa carandas L. (Apocynaceae); Rt Karaundath, Karonda Diarrhea, dysentery, bloody dysentery Taylor et al. 1996, Manandhar 1985
(T)
Cassia fistula L. (Fabaceae); Sd, Fr, Rt, St Rajbriksha (N), Stomachache, diarrhea, dysentery, diuretic, Bhattarai et al. 2009, Chapagain et al.
Aairogha (T) blisters, extreme thirst, blindness, throat 2004, Manandhar 2002, Dangol and
infection, skin diseases, syphilis, diabetes, Gurung 1991, Mandar and Chaudhary
asthma, laxative, headache, arthritis 1993
1985
Cynodon dactylon (L.) Pers. (Poaceae); WP, Dubho (N) Tonic, vertigo/dizziness, anthelmintic, Bhattarai et al. 2009, Acharya and
Rt, Lvs stomachache, defect in vision, toothache, Acharya 2009, Chapagain et al. 2004
cuts, boils, nasal bleeding, white leprosy
Cynoglossum lanceolatum Forssk. Cataracts Bhattarai et al. 2009
(Boraginaceae); Rt, Fl
Cynoglossum zeylanicum (Vahl.) Brand Chakchira (T) Headache, wounds, blisters Chapagain et al. 2004
(Boraginaceae); Lvs
Cyperus compressus L. (Cyperaceae); WP Jhusuna (T) Cuts, scabies Dangol and Gurung 1991
Cyperus difformis L. (Cyperaceae); WP Ghanaune chhatia (T) Earache Chapagain et al. 2004
Cyperus rotundus L. (Cyperaceae); Rt, Lvs Motha (N); Bhada (T) Stomach diseases, indigestion, diarrhea, Bhattarai et al. 2009, Acharya and
vomiting, cough, bronchitis, fever Acharya 2009
Dalbergia latifolia Roxb. (Fabaceae); Rt, Br Satisal (N) Bodyache Acharya and Acharya 2009
Dalbergia sissoo Roxb. ex DC. (Fabaceae); Sisso (N); Sisawa, Feeling of higher level of heat inside Bhattarai et al. 2009, Chapagain et
Br, Lvs, Sht Sisava (T) the body, impotency, cooling effect, al. 2004, Dangol and Gurung 1991,
anthelmintic, gout, fever Manandhar 1985, 1994
Datura metel L. (Solanaceae); Sd, Fr Dhatur (T) Mental disorders, diarrhea, dysentery, filaria Chapagain et al. 2004, Mandar and
Chaudhary 1993
Datura stramonium L. (Solanaceae); Sd, Lvs Dhaturo (N); Dhatur (T) Premature ejaculation, menstrual disorders, Bhattarai et al. 2009, Muller-Boker
bronchitis, arthritis 1999a, Mandar and Chaudhary 1993
Dendrocalamus hamiltonii Nees and Arn. ex Tama (N) Purgative Dangol and Gurung 1991
Munro (Poaceae); Sht
Desmodium gangeticum (L.) DC. (Fabaceae); Gatkosiya (T) Headache Bhattarai et al. 2009
Lvs, St, Fl
Desmodium laxiflorum DC. (Fabaceae); St Tangari (N) Abortification, fish poison Mandar and Chaudhary 1993
Desmostachya bipinnata (L.) Stapf (Poaceae); Kush (N), Kusli (T) Headache, toothache Chapagain et al. 2004
Rt
Dillenia pentagyana Roxb. (Dilleniaceae); Sd Tetari (N); Agai (T) Headache, to tick bites Chapagain et al. 2004, Muller-Boker
1999a
Dioscorea bulbifera L. (Dioscoreaceae); Tu Gittha tarul (N) Earache Chapagain et al. 2004
Dioscorea deltoidea Wall. ex Griseb. Gittha (Nep) Stomach pain Acharya and Acharya 2009
(Dioscoreaceae); Fr
Dioscorea sp. (Dioscoraceae); Rt Hardgohi (T) Fever Muller-Boker 1999a
Diospyros malabarica (Desr.) Kostel. Tendu (N) Boils Chapagain et al. 2004
(Ebenaceae); Fr
Diplocyclos palmatus (L.) C. Jeffrey Kundru (T) Blindness Chapagain et al. 2004
(Cucurbitaceae); Lvs
Diploknema butyracea (Roxb.) H.J. Lam Chyuri (N) Wounds, muscle pain, astringent Acharya and Acharya 2009,
(Sapotaceae); Fr, Sd Manandhar 1985
Drynaria quercifolia (L.) J. Sm. Hathajori (T) Arheya (a disease killing affected livestock) Muller-Boker 1999a
Medicinal Plants Used by the Tharu Communities in Nepal
(Polypodiaceae); WP
301
(Myrtaceae); Br
Eulaliopsis binata (Retz.) C.E. Hubb. Bankas (T) Blood purifier Chapagain et al. 2004
(Poaceae); WP
Euphorbia fusiformis Buch.-Ham. ex D.Don Banmurai (T) Body swelling, milk secretion Chapagain et al. 2004
(Euphorbiaceae); Tu
Euphorbia hirta L. (Euphorbiaceae); WP, Lvs, Duddhi (N); Dudhiya Constipation, cuts, milk secretion, wounds, Chapagain et al. 2004, Dangol and
Rt jhyang (T) blisters, numb legs Gurung 1991
Euphorbia parviflora L. (Euphorbiaceae); WP Sano duddhi (N) Menstrual problems Chapagain et al. 2004
Euphorbia prostrata Ait. (Euphorbiaceae); WP Dundhi (T) Snake-bite Manandhar 1985
Euphorbia royleana Boiss. (Euphorbiaceae); Sihundisighe, Sihur (T) Cough, cold, blisters, wounds, Bhattarai et al. 2009, Chapagain et al.
Lvs, Rt, St constipation, pneumonia, anthelmintic 2004, Manandhar 1994
Evolvulus nummularius (L.) L. Dinghumni phul (T) Scabies Manandhar 1985
(Convolvulaceae); WP
Ficus benghalensis L. (Moraceae); Br, Lvs Bargat, pipra (T) Diarrhea, dysentery, diabetes Acharya and Acharya 2009,
Chapagain et al. 2004, Mandar and
Chaudhary 1993
Ficus hispida L.f. (Moraceae); Lvs, Rt Kothaiya dumari (T) Diuretic, ear pain, ear wound, weakness of Bhattarai et al. 2009, Muller-Boker
hearing 1999a, Dangol and Gurung 1991
Ficus lacor Buch.-Ham. (Moraceae); Ltx Gular (T) Boils Manandhar 1985
Ficus racemosa L. (Moraceae); Ltx Gullar (T) Wounds, blisters Chapagain et al. 2004
Ficus religiosa L. (Moraceae); St, Lvs Pipal (N); Pipra (T) Cuts, wounds, body swelling, aching ear, Bhattarai et al. 2009, Chapagain et al.
regularize a woman’s monthly period, 2004, Muller-Boker 1999a, Dangol
migraine and Gurung 1991, Mandar and
Chaudhary 1993
Ficus semicordata Buch.-Ham. ex Sm. Khurhuri (T) Headache, fever, aching ear Acharya and Acharya 2009, Muller-
(Moraceae); Rt, Lvs, Twg Boker 1999a
Flemingia chappar Benth. (Fabaceae); Lvs, Rt Bansapti Cuts, diarrhea Chapagain et al. 2004
Flemingia macrophylla (Willd.) Merr. Majilauta (T) Toothbrush Muller-Boker 1999a
(Fabaceae); St
Flemingia strobilifera (L.) W.T.Aiton Banasapti Cuts Chapagain et al. 2004
(Fabaceae); Lvs
Fragaria indica Wall. (Rosaceae); WP Chauranchata (T) Fever, urinary disorders Dangol and Gurung 1991
Gardenia jasminoides J.Ellis (Rubiaceae); Fl Indrakaul Quench thirst Dangol and Gurung 1991
Garuga pinnata Roxb. (Burseraceae); Br, Sht Jhengra (T) Snake scorpion sting, cuts, diarrhea, boils, Chapagain et al. 2004, Manandhar
malaria, wounds 1985
Gaultheria fragrantissima Wall. (Ericaceae); Pakbherni (T) To get relief from par of head, legs and Acharya and Acharya 2009
Lvs hands
Medicinal Plants Used by the Tharu Communities in Nepal
Gmelina arborea Roxb. (Lamiaceae); Lvs Gamhar (T) Swelling Dangol and Gurung 1991
303
Hippochaete debilis (Roxb. ex Vaucher) Ching Sanohadchure (N) Bone fractures Bhattarai et al. 2009, Chapagain et
(Equisetaceae); WP al. 2004
Hiptage benghalensis (L.) Kurz Madhhulata (T) Toothache Chapagain et al. 2004
(Malpighiaceae); St
Holarrhena pubescens Wall. ex. G.Don. Dudhakoria, Kacheri (T) Bloody dysentery, diarrhea, worms, Bhattarai et al. 2009, Chapagain et al.
(Apocynaceae); Br, Fr, Ltx, Rt, Fl anthelmintic, snake scorpion sting, body 2004, Muller-Boker 1999a, Mandar
swelling, cough, cold, constipation, and Chaudhary 1993
tuberculosis, urinary infection, menstrual
disorders
Hydrocotyle rotundifolia Roxb. (Apiaceae); Tarpurin (T) Fever, urinary disorders Dangol and Gurung 1991
WP
Hygrophila auriculata (Schumach.) Heine Makhana (T) Toothache, body swelling, vomiting, Chapagain et al. 2004, Manandhar
(Acanthaceae); WP, Rt, Lvs wounds, blisters, invigorating 1985
Hymenodictyon orixense (Roxb.) Mabb. Bhudkul, Bhurkun (T) Body swelling, miscarriages Chapagain et al. 2004
(Rubiaceae); Sht, Fr
Ichnocarpus frutescens (L.) W.T.Aiton Chhekar duddhi (T) Diarrhea, milk seceretion Chapagain et al. 2004
(Apocynaceae); Rt, Lvs
Imperata cylindrica (L.) Raeusch. (Poaceae); Siru (N); Churki (T) Anthelmintic, cooling agent, vomiting, Chapagain et al. 2004, Muller-Boker
Rt anthelmintic 1999a, Manandhar 1994
Indigofera linifolia (L.f.) Retz. (Fabaceae); Rt Muscanna (T) Milk seceretion Chapagain et al. 2004
Inula cappa (Buch.-Ham. ex D.Don) Pataya (T) Headache, to reduce disorders arising due to Bhattarai et al. 2009
DC. (Asteraceae); Rt intake of meat
Ipomoea aquatic Forssk (Convolvulaceae); Dhodi (T) Wounds, blisters Chapagain et al. 2004
Lvs
Ipomoea carnea subsp. fistulosa (Mart. ex Besarma, Behaya (T) Cuts, wounds Chapagain et al. 2004, Manandhar
Choisg) D.F. Austin (Convolvulaceae); Ltx 1985
Ipomoea quamoclit L. (Convolvulaceae); WP Chhotaki gurubans (T) Blood vomiting Manandhar 1985
Isodon sp. (Lamiaceae); WP Mutmuhari (T) Infection Chapagain et al. 2004
Jatropha curcas L. (Euphorbiaceae); Ltx, St Sajiwan (N); Nijot, Wounds, blisters, burns, boils, gum Bhattarai et al. 2009, Chapagain et al.
Ramjeevanmam jyoti infection, athlete’s foot, tootache 2004, Muller-Boker 1999a, Dangol
(T) and Gurung 1991, Mandar and
Chaudhary 1993
Justicia adhatoda L. (Acanthaceae); Lvs, Sht, Asuro (N); Rus, Asur Body swelling, cough, cold, bronchitis, Chapagain et al. 2004, Dangol and
Rt (T) fever, asthma, bronchitis, typhoid, stomach Gurung 1991, Bhattarai et al. 2009,
pain Muller-Boker 1999a, Mandar and
Chaudhary 1993, Manandhar 1985
Justicia sp. (Acanthaceae); Lvs, WP Gorkatla, Panchuiya (T) Cooling agent, cuts, delivery Chapagain et al. 2004
Kalanchoe integra (Medik.) Kuntze Ajambari (N) Ear pain, ear wounds Bhattarai et al. 2009
(Crassulaceae); Lvs
Medicinal Plants Used by the Tharu Communities in Nepal
(Lamiaceae); Rt, WP, Lvs (T) boils, urinary complaints Gurung 1991, Manandhar 1985
Leucas zeylanica (L.) W.T.Aiton (Lamiaceae); Dulphi Jaundice Mandar and Chaudhary 1993
Lvs
Linum usitatissimum L. (Linaceae); WP, Sd Arasi (T) Wounds, boils Manandhar 2002
Lippia nodiflora (L.) Rich. (Verbenaceae); WP Kokan (T) Headache Manandhar 1985
Litchi chinensis Sonn. (Sapindaceae); Ltx Litchi (N) Dysentery Bhattarai et al. 2009
Litsea monopetala (Roxb.) Pers. (Lauraceae); Kutmero (N) Stomachache Bhattarai et al. 2009
Sd
Ludwigia octovalvis (Jack.) Raven Bihi (N) Wounds Manandhar 1985
(Onagraceae); WP
Luffa cylindrica (L.) M. Roem. Ghira (T) Chicken pox Muller-Boker 1999a
(Cucurbitaceae); Sd
Lygodium flexosum (L.) Sw. (Lygodiaceae); Rt Bhalunia Wounds, blisters Chapagain et al. 2004
Macrotyloma uniflorum (Lam.) Verdc. Gahat (T) Arthritis/Rheumatism Chapagain et al. 2004
(Fabaceae); Sd
Madhuca longifolia (J.Koenig ex L.) Mahuwa (N) Tierdness Mandar and Chaudhary 1993
J.F.Macbr. (Sapotaceae); Fl
Mallotus philippensis (Lam.) Mull. Arg. Sindure (N); Rohini (T) Diarrhea, dysentery, asthma, bronchitis, Bhattarai et al. 2009, Chapagain et al.
(Euphorbiaceae); Br, Rt, Fr urinary tract infection, constipation, skin 2004, Dangol and Gurung 1991
diseases, typhoid, gastratis
Mangifera indica L. (Anacardiaceae); Br, Ltx, Aamp (N) Chronic diarrhea, gastritis, dysentery, loss Bhattarai et al. 2009, Chapagain et al.
Rt, Fr of weight, vitamin deficiency, menstrual 2004, Mandar and Chaudhary 1993
disorders
Marsdenia tinctoria R.Br. (Apocynaceae); Fl Dudhe laharo (N) Gout, disorder of thymus, to purify blood Acharya and Acharya 2009
Melia azedarach L. (Meliaceae); Br, Rt, Fr, Bakaino, Nimpata (N); Diarrhea, cholera, constipation, anthelmintic, Bhattarai et al. 2009, Acharya and
Lvs Bakain (T) vomiting, blood impurities, urinary Acharya 2009, Dangol and Gurung
discharges, fever, paralysis 1991, Mandar and Chaudhary 1993
Mentha arvensis L. (Lamiaceae); Lvs Patina (N) Cough, cold, dehydration, gastritis Bhattarai et al. 2009
Mentha longifolia (L.) L. (Lamiaceae); Lvs Pudina (N) Headache, cooling agent, dysentery, skin Chapagain et al. 2004
diseases
Mentha spicata L. (Lamiaceae); Lvs Bawari, Pudina (N) Throat infection, indigestion, boils Acharya and Acharya 2009,
Manandhar 1985
Mimosa pudica L. (Fabaceae); Rt Lajjawati (N); Cuts, wounds, insomnia, fever, paralysis Bhattarai et al. 2009, Chapagain et al.
Lajmohani (T) 2004, Mandar and Chaudhary 1993
Mirabilis jalapa L. (Nyctaginaceae); Rt Malati phul (N); Delivery problems, menstrual problems, Chapagain et al. 2004, Manandhar
Nakesari, Barka milk seceretion, nasal bleeding, scabies 1985
gurubans (T)
Table 15.1 contd. …
Medicinal Plants Used by the Tharu Communities in Nepal
307
…Table 15.1 contd.
Plant’s Scientific Name (family name); Nepali and Tharu Medicinal Usage References
Parts Used names
Momordica charantia L. (Cucurbitaceae); WP, Kareli jhar (N) Body swelling, blindness Chapagain et al. 2004
Lvs
Momordica dioica Roxb. ex Willd Kheksi (T) Diabetes, urinary infection Chapagain et al. 2004
(Cucurbitaceae); Rt
Moringa oleifera Lam. (Moringaceae); Fr, Munga (N) Blood pressure Mandar and Chaudhary 1993
Lvs, Br
Morus serrata Roxb. (Moraceae); Rt, Br Tathimashlari (T) Diarrhea, anthelmintic, typhoid Bhattarai et al. 2009
Murraya koenigii (L.) Spreng. (Rutaceae); Fr, Ban neem, binbinbheria Diarrhea, dysentery Acharya and Acharya 2009,
Lvs, Rt (T) Chapagain et al. 2004
Musa paradisiac L. (Musaceae); Fr, St Kera (N) Loss of weight, diarrhea, dysentery Chapagain et al. 2004, Mandar and
Chaudhary 1993
Myrica esculenta Buch.Ham ex D.Don Kafal (N) Dysentery Chapagain et al. 2004
(Myricaceae); Br
Nelumbo nucifera Gaertn. (Nelumbonaceae); Kamalko phul (N) Pneumonia Chapagain et al. 2004
St
Neopicrorhiza scrophulariflora (Pennell) Kutki (N) Cuts Chapagain et al. 2004
308 ETHNOBOTANY: Local Knowledge and Traditions
D.Y.Hong (Plantaginaceae); Rt
Nepeta leucophylla Benth. (Lamiaceae); WP Gandheli gharra (T) Boils Manandhar 1985
Nicotiana tabacum L. (Solanaceae); Lvs Surti (N) Swelling of scrotum and testes Bhattarai et al. 2009
Nyctanthes arbortristis L. (Oleaceae); Fl, Lvs Parijat (N) Headache Chapagain et al. 2004
Ocimum americanum L. (Lamiaceae): Rt Bawari (N) Fever Manandhar 1985
Ocimum basilicum L. (Lamiaceae); Sd Gathiwan (T) Cough, cold, feeling of higher level of heat Bhattarai et al. 2009
inside the body
Ocimum tenuiflorum L. (Lamiaceae); Lvs Tulsi (N) Blood pressure, wounds, ear pain, cough, Bhattarai et al. 2009, Chapagain et al.
cold, bronchitis, sinusitis, typhoid, fever 2004, Mandar and Chaudhary 1993
Opuntia monacantha (Willd.) Haw. Pate siundi (N) Burns, boils, wounds, blisters Chapagain et al. 2004
(Cactaceae); St, Sap
Oroxylum indicum (L.) Kurz (Bignoniaceae); Sauna tata (T) Bone fracture, dysentery, pneumonia, Chapagain et al. 2004, Muller-Boker
Rt, Fr, Br vomiting, wounds, menstrual disorders 1999a, Mandar and Chaudhary 1993
Oxalis corniculata L. (Oxalidaceae); WP, Lvs, Chariamilo (N), Fever, diarrhea, boils, dysentery, fever, Bhattarai et al. 2009, Acharya and
St, Rt Chamchama, Amchocha pneumonia, wounds, blisters, nasal bleeding, Acharya 2009, Chapagain et al. 2004,
(T) relieves pains, cold Muller-Boker 1999a, Dangol and
Gurung 1991
Parmelia nepalensis Tayl. (Parmeliaceae); WP Jhyau (N) Diseases of gum, throat, scabies, piles, Acharya and Acharya 2009
leprosy
Pericampylus glaucus (Lam.) Merr. Khuranijhar (N) Diuretic, dysuria Bhattarai et al. 2009
(Menispermaceae); Rt
Peristrophe bicalyculata (Retz.) Nees ChuChure (T) Fever, cuts, wounds Taylor et al. 1996
(Acanthaceae); WP
Persicaria barbata (L.) H.Hara Miriya bikh (T) Swelling Dangol and Gurung 1991
(Polygonaceae); WP
Phyla nodiflora (L.) Greene (Verbenaceae); Jalnim, Jhyangrin (T) Headache, appetizer, cooling agent, Chapagain et al. 2004, Dangol and
Rt, Lvs, WP stomachache, ulcers Gurung 1991
Phyllanthus amarus Schumach. and Thonn. Bhuiamala (N); Asthma, bronchitis, Bhattarai et al. 2009, Manandhar
(Phyllanthaceae); WP, Rt, Lvs Chhotaki dahigola (T) urinary tract infection, diuretic, stomachic, 1985, 2002
febrifuge, pimples, cuts, wounds
Phyllanthus emblica L. Amala(N); Aura, Heart pain, constipation, cough, cold, Bhattarai et al. 2009, Acharya and
(Phyllanthaceae); Fr, Sd, St, Lvs Auraha, Yawara (T) sinusitis, Acharya 2009, Chapagain et al. 2004,
diarrhea, dysentery, gastritis, diuretic, Muller-Boker 1999a, Mandar and
laxative, vitamin, burns, hair tonic Chaudhary 1993
Phyllanthus urinaria L. (Phyllanthaceae); Rt, Sano dahigola (T) Wounds, blisters Chapagain et al. 2004
Lvs
Physalis divaricata D.Don (Solanaceae); WP Galbhomara (T) Body thin and feeble Manandhar 1985
Medicinal Plants Used by the Tharu Communities in Nepal
Piper cubeba L.f. (Piperaceae); Fr Marich (N) Boils, cough, cold, Bhattarai et al. 2009
tonsillitis, bronchitis, wounds
Piper longum L. (Piperaceae); Rt, Fr, St Kharipipar, Pharipipra Menstrual disorders, cough, digestion, Bhattarai et al. 2009, Acharya and
(T) asthma, cold Acharya 2009, Chapagain et al. 2004,
Muller-Boker 1999a, Dangol and
Gurung 1991
Plantago major L. (Plantaginaceae); Sd Bhatbhadwa (T) Fever, diarrhea, dysentery, laxative Acharya and Acharya 2009
demulcent, expectorant, diuretic
Plumbago zeylanica L. Abijale kuro (N); Blister, wart, ringworm, Bhattarai et al. 2009, Manandhar
(Plumbaginaceae); Ltx, WP, Rt Kalamnath (T) diarrhea, dysentery, fever, stomachache, 1985, 1987b, 1990
boils, stomach disorders
Plumeria rubra L. (Apocynaceae); St, Ltx, Br Galaini (N) Stomachache, rabies infection toothache, Bhattarai et al. 2009, Chapagain et
anthelmintic al. 2004
310 ETHNOBOTANY: Local Knowledge and Traditions
Pogostemon benghalensis (Burm.f.) Kuntze Rudhilo (Nep); Bhati, Fever, cough, cold, typhoid, bodyache, Bhattarai et al. 2009, Chapagain et al.
(Lamiaceae); WP, Rt, Sd, Lvs Udhara, Kohabar (T) diarrhea, pneumonia, dysentery 2004, Manandhar 1985, 1988
Pogostemon parviflorus Benth. (Lamiaceae); Utajari (T) Fever Dangol and Gurung 1991
Lvs
Polyalthia longifolia (Sonn.) Thw. Ashoka (N) Delivery Chapagain et al. 2004
(Annonaceae); Br
Polygala arillata Buch.-Ham. ex D.Don Thanak (T) Tonsillitis, stomachache, gastritis, cough, Bhattarai et al. 2009
(Polygalaceae); WP cold, wounds
Polygonatum verticillatum (L.) All. Kaituwa (T) Tonic Manandhar 1988
(Asparagaceae); Rt
Polygonum plebejum R.Br. (Polygonaceae); Chiraik gor (T) Wounds Manandhar 1985
WP
Polygonum viscosum (Buch.-Ham ex D.Don) Biria (T) Inflammation of sex organs of child Chapagain et al. 2004
(Polygonaceae); Lvs
Pouzolzia zeylanica (L.) Benn. (Urticaceae); Kakara khopta, Ringworm, wounds Dangol and Gurung 1991
WP Kakarakucha
Premna barbata Wall. ex Schauer Giliyar (T) Fever, quench thirst Dangol and Gurung 1991
(Lamiaceae); St Br
Premna serratifolia L. (Lamiaceae); Rt, Lvs Gineri (N) Body swelling, wounds, blisters Chapagain et al. 2004
Prunus persica (L.) Batsch (Rosaceae); Lvs Aru (N) Wounds Bhattarai et al. 2009, Chapagain et
al. 2004
Psidium guajava L. (Myrtaceae); Br, Fr, St, Amba, Belauti (N); Diarrhea, dysentery, constipation, fever, Bhattarai et al. 2009, Chapagain et al.
Lvs, Rt Runi, amrud (T) cough, cold, anthelmintic, hoarseness 2004, Muller-Boker 1999a, Mandar
of voice, vomiting, tootache, stomach and Chaudhary 1993, Manandhar
complaints 1985
Pterocarpus marsupium Roxb. (Fabaceae); Bijaya sal (N) Neurological problems, pneumonia Acharya and Acharya 2009
St, Br
Pulicaria dysenterica (L.) Gaertn. Gandhaiya (T) Wounds Manandhar 1985
(Asteraceae); WP
Punica granatum L. (Lythraceae); Fr, Br Darim, Anar (Nep) Diarrhea, dysentery, skin abrasions, control Bhattarai et al. 2009, Mandar and
abortion, miscarriage Chaudhary 1993
Ranunculus sceleratus L. (Ranunculaceae); Nakapolba (T) Gastric inflammation Manandhar 1985
WP
Raphanus sativus var. bortensis Backer Mula (N) Indigestion, skin diseases Chapagain et al. 2004
(Brassicaceae); Lvs, Tu
Rauvolfia serpentina (L.) Benth. ex Kurz Sarpagandha Cuts, wounds, boils, fever, stomachache, Bhattarai et al. 2009, Acharya and
(Apocynaceae); Rt, Fr (N); Dhaldhaliya, menstrual disorders, snake bite, blood Acharya 2009, Chapagain et al. 2004,
Dharmarua, pressure, hypotonic, dysentery, indigestion, Manandhar 1985, 1988, Muller-Boker
Medicinal Plants Used by the Tharu Communities in Nepal
Dhambarbiruwa (T) mental disorders, diarrhea 1999a, Dangol and Gurung 1991
Table 15.1 contd. …
311
…Table 15.1 contd.
Plant’s Scientific Name (family name); Nepali and Tharu Medicinal Usage References
Parts Used names
Reinwardtia indica Dumort. (Linaceae); Rt Dauthi Phul (N) Lactation Bhattarai et al. 2009
in postpartum mothers
Remusatia vivipara (Roxb.) Schott (Araceae); Kachchu (N) Boils, blisters Mandar and Chaudhary 1993
St
Ricinus communis L. (Euphorbiaceae); Sd, Andir (N); Reyar, Reru Skin abrasions, to relieve pain on fractured Bhattarai et al. 2009, Chapagain et al.
Lvs, Fr, St, Rt (T) bone, body swelling, deafness, burn, 2004, Muller-Boker 1999a, Mandar
constipation, boils and Chaudhary 1993, Manandhar
1985
Rumex nepalensis Spreng. (Polygonaceae); Sd Dhaldhaliya (T) Chickenpox Manandhar 1985
Sagittaria guayanensis Kunth (Alismataceae); Banarbhega (T) Fever Manandhar 1985
WP
Sapium insigne (Royle) Benth. Khirro (N) Diarrhea Manandhar 1985
(Euphorbiaceae); Ltx
Saraca asoca (Roxb.) Willd. (Fabaceae); Br Aasho Diarrhea, dysentery, pimples, stomachic Mandar and Chaudhary 1993
Schefflera venulosa (Wight & Arn.) Harms Simarlati (T) Irregular menstrual cycle Muller-Boker 1999a
(Araliaceae); Twg
312 ETHNOBOTANY: Local Knowledge and Traditions
Schima wallichii Choisy (Theaceae); Br Chilaunee (N) Wounds, diarrhea, dysentery Bhattarai et al. 2009
Schleichera oleosa (Lour.) Mers. Kusum (N) Ulcer Chapagain et al. 2004
(Sapindaceae); Br
Scoparia dulcis L. (Plantaginaceae); Lvs, WP Chiniya jhyang (N); Diabetes, fever, great thirst, cooling, Chapagain et al. 2004, Muller-
Gurikijhani, Bhera diarrhea, dysentery, mental disorders, boils Boker 1999a, Dangol and Gurung
chachura (T) 1991, Mandar and Chaudhary 1993,
Manandhar 1985
Scurrula elata (Edgew.) Danser Aainjeru (N) Joint pain Acharya and Acharya 2009
(Loranthaceae); Lvs
Semecarpus anacardium L.f. (Anacardiaceae); Bhela (T) Dysentery, asthma, acute rheumatism, cuts, Acharya and Acharya 2009,
Fr chapped feet Chapagain et al. 2004, Manandhar
1985
Senna occidentalis (L.) Link (Fabaceae); Rt Bangain (T) Ringworm infection Dangol and Gurung 1991
Senna tora (L.) Roxb. (Fabaceae); Tapra (N), Chakon, Headache, toothache, snake scorpion Bhattarai et al. 2009, Chapagain
Lvs, St, Fr, Rt, Sd Chilbile (T) sting, skin diseases, cough, leprosy, fever, et al. 2004, Manandhar 1985, 1986b,
anthelmintic 1987b, 1990, 1994
Sesamum indicum L. (Pedaliaceae); Sd, Rt Til (N) Arthritis/rheumatism Chapagain et al. 2004
Shorea robusta Gaertn. (Dipterocarpaceae); Sal (N); Sakuwa (T) Diarrhea, bloody dysentery, cuts, appetizer Bhattarai et al. 2009, Chapagain
Ltx, Sd, Res, Lvs et al. 2004, Muller-Boker 1999a,
Manandhar 1985
Sida cordata (Burm.f.) Borss Waalk. Biskhopra, Baliyari (T) Snake scorpion sting, body swellings, Chapagain et al. 2004, Dangol and
(Malvaceae); Lvs, St, Rt wounds, blisters, boils, tonic Gurung 1991, Manandhar 1985
Sida rhombifolia L. (Malvaceae); Lvs, Rt, WP Barchar, Biskhopra, Snake scorpion sting, cuts, loss of weight, Chapagain et al. 2004, Muller-Boker
Balu jhar (T) bruises, wounds, boils 1999a, Manandhar 1985
Smilax ovalifolia Roxb. ex D.Don Bagnucha (T) Dysentery, blindness Chapagain et al. 2004
(Smilacaceae); Rt, St
Solanum aculeatissimum Jacq. (Solanaceae); Ghorhyenta (T) Toothache, fever Dangol and Gurung 1991
Fr
Solanum americanum L. (Solanaceae) Fr, Rt Kanthakari, bihi (N); Headache, asthma, cooling agent, eye Bhattarai et al. 2009, Chapagain et al.
Bhutka complaints 2004, Mandar and Chaudhary 1993
Solanum anguivi Lam. (Solanaceae); Fr, WP Sanobihi (Nep) Headache, insomnia Bhattarai et al. 2009, Manandhar 1985
Solanum erianthum D.Don (Solanaceae); Fr Bhurakath (T) Cough, cold Chapagain et al. 2004
Solanum surattense Brum.f. (Solanaceae); Fr Kacharehata (T) Decaying teeth Manandhar 1985
Solanum torvum Swartz (Solanaceae); Fr Bihi (N) Headache Manandhar 1985
Solanum tuberosum L. (Solanaceae); Tu Alu (N) Snake scorpion sting, boils Chapagain et al. 2004, Mandar and
Chaudhary 1993
Solanum virginianum Dunal (Solanaceae); Khasretha (T) Toothache Chapagain et al. 2004
Lvs, Sd
Medicinal Plants Used by the Tharu Communities in Nepal
(Myrtaceae); Br
Syzygium operculata (Roxb.) Neid. Bhadra jam (T) Cuts, diarrhea, hoarseness of voice, measles Chapagain et al. 2004
(Myrtaceae); Br, Rt, Sht, Lvs
Tagetes erecta L. (Asteraceae); Lvs Gendaphul Diarrhea, dysentery Mandar and Chaudhary 1993
Tamarindus indica L. (Fabaceae); Lvs Yemili (T) Cuts, wounds, diarrhea, dysentery Dangol and Gurung 1991, Mandar
and Chaudhary 1993
Tectona grandis L.f. (Lamiaceae); Br Sagun (T) Menstrual disorders Chapagain et al. 2004
Terminalia alata Heyne ex Roth Saj (N); Asna (T) Diarrhea, dysentery, stomachache Bhattarai et al. 2009
(Combretaceae); Br
Terminalia arjuna (Roxb. ex DC) W. and A. Arjun Kaath Bodyache Chapagain et al. 2004
(Combretaceae); Ltx
Terminalia bellirica (Gaertn.) Roxb. Barro (N), Asida, Baheri Cough, cold, appetizer, gastritis, diarrhea, Bhattarai et al. 2009, Chapagain et al.
(Combretaceae); Fr (T) dysentery, 2004, Muller-Boker 1999a, Dangol
Stomachache, constipation, eye diseases, and Gurung 1991, Mandar and
bronchitis Chaudhary 1993
Terminalia chebula Retz. (Combretaceae); Fr Harro (N); Harai (T) Cough and cold, gastritis, bronchitis, chest Bhattarai et al. 2009, Chapagain et al.
pain, diarrhea, dysentery 2004, Muller-Boker 1999a, Mandar
and Chaudhary 1993
Tetrastigma serrulatum (Roxb.) Planch. Tinpatiya (T) Wounds, blisters Chapagain et al. 2004
(Vitaceae); Lvs
Thevetia peruviana (Pers.) K. Schum. Karbir (N Ear pain, wounds Bhattarai et al. 2009, Dangol and
(Apocynaceae); Lvs, Fr Gurung 1991
Thysanolaena maxima (Roxb.) Kuntze Bashadi, Bankucho (T) Boils, anthelmintic Bhattarai et al. 2009
(Poaceae); Rt
Tiliacora sp. (Menispermaceae); Rt Karot (T) Anthelmintic Chapagain et al. 2004
Tinospora sinensis (Lour.) Merr. Gurjo (N) Diarrhea, dysentery, stomachache, diuretic Bhattarai et al. 2009
(Menispermaceae); Rt
Torenia sp. (Linderniaceae); WP Sauna phul (T) Wounds, blisters Chapagain et al. 2004
Trachyspermum ammi (L.) Sprague Jawain (T) Colds, sore throat, wounds, pimples, rashes, Muller-Boker 1999a
(Apiaceae); Sd, WP pneumonia, diarrhea
Trianthema protulacastrum L. (Aizoaceae); Rt Gaspurna (T) Body swelling Chapagain et al. 2004
Trichodesma indicum (L.) Lehm. Oonmodia jhyang (T) Headache Dangol and Gurung 1991
(Boraginaceae); WP
Trichosanthes dioica Roxb. (Cucurbitaceae); Parwar (N) Hand/leg ache Chapagain et al. 2004
Rt
Tridax procumbens L. (Asteraceae); Fl, WP Dhusere (N) Cough, cold, boils Manandhar 1985
Triumfetta rhomboids Jacq. (Tiliaceae): WP Bishakhopra (T) Boils, pimples Manandhar 1985
Keys: N: Nepali; T: Tharu; Lvs: Leaves; Fr: Fruits; Sd: Seeds; Rt: Roots; Rh: Rhizomes; Br: Barks; WP: Whole plant; Ltx: Latex; Sht: Shoots; Fl: Flowers;
Tu: Tubers; Psb: Pseudobulb; Arp: Aerial parts; Bd: Buds; SP: Spines; Twg: Twigs; Bu: Bulbs.
Medicinal Plants Used by the Tharu Communities in Nepal
317
318 ETHNOBOTANY: Local Knowledge and Traditions
35
30
25
Number of species 20
15
10
ae
ae
ae
ae
ae
e
ae
ae
e
ea
ea
ce
ce
ea
ce
ce
ce
ce
ce
ac
ac
ta
ba
ac
ia
va
na
ra
na
bi
bi
m
Po
or
te
Fa
al
la
or
cy
ur
La
M
As
M
So
ph
uc
po
Eu
C
A
Family
Fig. 15.5. Top ten largest families used for medicine by the Tharu communities in Nepal.
Tubers 1% Twings
Others 2%
Shoots 2% 1%
Latex 3%
Flowers 4%
Seeds 6% Roots/Rhizomes
21%
Stems 7%
Fruits 11%
Wholeplant 14%
Fig. 15.6. Plant parts used in medicine by the Tharu communities in Nepal.
Conclusion
The Guruwas (traditional healers) of the Tharu community have a vast knowledge
of the medicinal value of the plants. Even today medicinal plants are widely used
in the Tharu communities to treat common ailments. But the social survival of
those people is disappearing day by day. Tharu people are highly linked with the
bioresources and the preservation and protection of those resources are essential
to preserve their cultural and ethnobotanical knowledge. Through a Nepalese
perspective, community participation has long been tested and considered successful
for the protection and conservation of bioresources. Hence, the government should
320 ETHNOBOTANY: Local Knowledge and Traditions
update such policy which will be helpful to preserve the traditional healing practices
of the several ethnic communities, including the Tharus of Nepal.
References
Acharya, R. and Acharya, K.P. 2009. Ethnobotanical study of medicinal plants used by tharu community
of parroha VDC, Rupandehi district, Nepal. Sci. Word 7(7): 80–84.
Baral, S.R. and Kurmi, P.P. 2006. A Compendium of Medicinal Plants in Nepal. Mass Printing Press,
Chhauni, Kathmandu.
Bhattachan, K. 2016. Post-shifting cultivation: struggles for livelihood and food security among Tharu
people displaced by the Chitwan national park in Nepal. pp. 291–325. In: Christian, E. (ed.).
Shifting Cultivation, Livelihood and Food Security: New and Old Challenges for Indigenous
Peoples in Asia. Bangkok: The Food and Agriculture Organization of the United Nations,
International Work Group for Indigenous Affairs and Asia Indigenous Peoples Pact.
Bhattarai, S. 2009. Ethnobotany and antibacterial activities of selected medicinal plants of Nepal
Himalaya. PhD. Thesis, Central Department of Botany, Tribhuvan University, Kirtipur, Kathmandu,
Nepal.
Bhattarai, S.B., Chaudhary, R.P. and Taylor, R.S.L. 2009. Ethnomedicinal plants used by the people of
Nawalparasi District, Central Nepal. Our Nat. 7: 82–99.
Bista, D.B. 2004. People of Nepal. Ratna Pustak Bhandar, Kathmandu, Nepal.
Chapagain, D.J., Joshi, S.D. and Jnawali, S.R. 2004. Use of medicinal plants by Tharu community in
the southwestern bufferzone of Royal Bardiya National park. Sci. Word. 2(2): 50–62.
Chaudhary, R.P. 1998. Biodiversity in Nepal: Status and Conservation. S. Devi, Saharanpur (U.P.),
India and Tecpress Books Bangkok, Thailand.
Dangol, D.R. and Gurung, S.B. 1991. Ethnobotany of the Tharu tribe of Chitwan District, Nepal. Int.
Journ. Pharmacog. 29(3): 203–209.
Ghimire, K. and Bastakoti, R. 2009. Ethnomedicinal knowledge and healthcare practices among the
Tharus of Nawalparasi district in central Nepal. For. Ecol. Manage. 257(10): 2066–2072.
GON. 2006. Plants of Nepal: Fact Sheet. Government of Nepal, Ministry of Forest and Soil Conservation,
Department of Plant Resources, Thapathali, Kathmandu, Nepal.
Gurung, H. 1996. Ethnic Demography of Nepal. Kathmandu: Nepal Foundation Paper 5, Nepal
Foundation for Advanced Studies.
Hagen, T. 1960. Nepal, Konigreich am Himalaya, Bern, Kummerly and Frey.
Krauskopff, G. 1995. The anthropology of the Tharus: an annoted bibliography. Kail. 17(3/4): 185–213.
Katewa, S.S., Chaudhary, B.L. and Jain, A. 2004. Folk herbal medicines from tribal area of Rajasthan,
India. Jour. Ethnophar. 92: 41–46.
Lall K. 1983. The Tharus. The Rising Nepal 20(233): 3
Lewis, M.P., Simons, G.F. and Fennig, C.D. (eds.). 2014. Tharu, Chitwania: a language of Nepal.
Ethnologue: Languages of the World, Seventeenth edition. Dallas, Texas: SIL International,
online version.
Mahishi, P., Srinivasa, B.H. and Shivanna, M.B. 2005. Medicinal plant wealth of local communities
in some villages in Shimoga district of Karnataka, India. Journ. Ethnopharmo. 98: 307–312.
Manandhar, N.P. 1985. Ethnobotanical notes on certain medicinal plants used by Tharus of Dang-
deokhuri district, Nepal. Int. J. Crude Drug Res. 23(4): 153–159.
Manandhar, N.P. 1986b. Ethnobotany of Jumla district, Nepal. Int. J. Crude Drug Res. 24(2): 81–89.
Manandhar, N.P. 1987a. Traditional medicinal plants used by tribals of Lamjung district, Nepal. Int. J.
Crude Drug Res. 25(4): 236–240.
Manandhar NP. 1988. Ethno Veterinary medicinal drugs of Central development region of Nepal. Bull.
of Med. Ethno. Bot. Res. 10(3-4): 93–99.
Manandhar, N.P. 1989a. Medicinal plants used by Chepang tribes of Makawanpur district, Nepal.
Fitoter. 60(1): 61–68.
Manandhar, N.P. 1989b. Useful wild plants of Nepal. Franz Steiner Verlag Wiesbaden GMBH, Stuttgart,
W Germany.
Medicinal Plants Used by the Tharu Communities in Nepal 321
Manandhar, N.P. 1990. Folk-lore Medicine of Chitwan District, Nepal. Ethnob. 2: 31–38.
Manandhar, N.P. 1994. Medicinal Folk-lore about the plants used as anthelmintic agents in Nepal.
Fitother. 16(2): 149–155.
Manandhar, N.P. 2002. Plants and People of Nepal. Timber Press, Portland, Oregon.
Mandar, L.N. and Chaudhary, R.P. 1993. Medicinal Plants and their traditional use by tribal people
of Saptari district, Nepal. In: Proceedings of First National Botanical Conference (1992). Nepal
Botanical Society, Kathmandu.
McDonaugh, C. 2007. Spirit, substance, vehicle. Kinship and cosmology among the Dangaura Tharu,
Nepal.
McLean, J. 1999. Conservation and the Impact of Relocation on the Tharus of Chitwan, Nepal, Himalaya.
The Journ. Assoc. Himalay. Studi. 19(2): 38–44.
Meyer, K.W. and Deuel, P. 1999. Who are the Tham? National Minority and Identity as manifested in
Housing forms and Practices. In: Skar, H.O. (ed.). Nepal: Tharu and Tarai Neighbours, Kathmandu:
Bibliotheca Himalayica.
Muller-Boker, U. 199l. Wild Animals and Poor people: Conflicts between Conservation and Human
needs in Citawan (Nepal). Europ. Bullet. Himalay. Res. 2: 28–31.
Muller-Boker, U. 1993. Ethnobotanical Studies among the Citawan Tharus. Journ. Nep. Rese. Cent.
9: 17–56.
Müller-Böker, U. 1999a. The Chitawan Tharus in Southern Nepal. An Ethnoecological Approach. Nepal
Re-search Centre Publications, No. 21. Kathmandu, Stuttgart.
Müller-Böker, U. 1999b. The Chitwall Tharus ill Southern Nepal: All Ethnoecological Approach. Franz
Stiner Verlag Stuttgart.
Pyakuryal, K. 1982. Ethnicity and Rural Development: A Sociological Study of Four Tharu Villages
in Chitwan, Nepal. PhD. Thesis, Michigan State University.
Rajaure, D.P. 1975. Tatooing among the Tharus of Dang-Deokhuri, Far western Nepal. Contri. Nepal.
Stud. 2(1): 91–98.
Sapkota, M. 2014. Contested Identity Politics in Nepal: Implications from Tharu Movement. IOSR
Journ. Humanit. Soci. Sci. 19(7): 16–25.
Shrestha, P. 1985. Research note: Contribution to the ethnobotany of the Palpa area. Contr. Nepal.
Stud. 12(2): 63–74.
Skar, H.O. (ed.). 1999. Nepal: Tharu and Tarai Neighbours. Kathmandu: Bibliotheca Himalayica.
Taylor, R.S.L., Hudson, J.B., Manandhar, N.P. and Towers, G.H.N. 1996. Antiviral activities of medicinal
plants of southern Nepal. Journ. Ethnophar. 53: 97–104.
Thapa, S. 2001. Documentation of Traditional Uses of Plants by Tharu Community around Royal
Shuklaphanta Wildlife Reserve, Far-Western Nepal. MSc Dissertation, Central Department of
Botany, Tribhuvan University, Kathmandu, Nepal.
Verma, S.C. 2010. The eco-friendly Tharu tribe: A study in socio-cultural dynamics. Journ. Asi. Pac.
Stud. 1(2): 177–187.
Index
A D
administration 191, 192 Dakshin Dinajpur 132–134, 137, 138, 151–154
aerial parts 194–207 Dioscorides 37
Agroecology 19, 20 diuretic 194–197, 199–203, 205, 207
Alkaloid 12, 171, 173, 175, 176
ancient therapeutic practices 188 E
angiosperm 137, 151, 153
emenagogue 194, 196, 198, 201, 202, 204, 205
anthelmintic 194, 195, 197, 198, 201–204
Erythroxylum coca 199
antidiarreheic 194
Ethnobotany 1, 34–37, 40–42, 46, 47, 52, 71,
antiophidic 103, 104, 119–122
75, 84, 85, 132, 133, 152, 214, 219
antioxidant 51, 53, 57–62, 265, 266
Ethnography 34
Antipsoriatic Agents 159, 160, 173
Ethnology 34, 36, 38
Antivenom plants 103
ethnomedicinal uses 260
Argentina 187, 188, 191, 193, 209–211
Ethnomedicine 35, 187, 289
Aspidosperma quebracho-blanco 191, 195
Ethnopharmacobotany 34, 35, 43, 46, 47
Asteraceae 195, 208, 211
ethnopharmacological knowledge 187
B Ethnopharmacology 42, 43, 46, 187
Ethnoscience 35, 36, 43, 47
Baccharis salicifolia 195, 210–212
barks 196 F
bio piracy 70
Fabaceae 199, 208, 211
bioactive compounds 103, 105, 106, 108, 110,
febrifuge 194–209, 211
112, 114, 116, 118, 119, 121
flavonoid 264, 266
Biodiversity 20, 23, 29, 187, 211
food 50, 51, 54, 61–63
blood depurative 206
fruits 196–198, 200, 203–205, 211
Brosimum acutifolium Huber 1, 6, 9, 11
Buddlejaceae 197
G
Bufotenine 12
bulb 193, 207 gathering practices 56, 58
Bulnesia sarmientoi 206 GC-MS analysis 264, 265
genetic resources 70
C Genus Teucrium 215, 218, 219, 224, 225, 227
Geoffroea decorticans 191, 200
Chaqueño domain 189
Commelina erecta 206, 210, 212
H
conservation 233, 236, 243, 245, 246, 250
Herbaria 35, 43–46
324 ETHNOBOTANY: Local Knowledge and Traditions
I P
Ilex paraguariensis 193, 195 Paraguay 232–240, 243–245, 247, 248, 250
Peasants 19–21, 24, 25, 28–30
J phenolics 173
Phytogeographic 188–191, 211
Jesuits 4, 7, 9
Poaceae 255–257
preparation 192, 193, 211
K
Psoriasis 158–161, 171–176, 178–182
Khas grass 256–258, 260, 267, 270
R
L
Ricinus communis 199
Latin America 187 roots 194, 195, 199–207
leaves 192–207, 209–211 Rural community 19, 20, 31
Leschenault de la Tour 43 Rutaceae 203, 208, 211
Lilaceae 207
S
M
Saponin 12–14
Mapuche Pharmacopoeia 91, 95 Schinus molle 209, 210, 212
Mate 193, 212 Schultes 36, 41, 42
Materia Medica 37, 44 scientific studies 275–278, 280, 282, 284
medicinal plant 70–76, 78, 79, 82–86, 158–161, seeds 194, 195, 197, 198, 200–202, 204, 207, 210
171, 172, 178, 179, 181, 232–237, Socio-ecological management 20
239–251 subterranean organs 90, 93
medicine 63, 65, 191, 192 Syphilis 1–6, 9, 11–14
Mentha spicata 201
Mocoví 189, 190, 193, 194 T
Mocovíes 187, 189, 191, 192, 209, 211
Teofrasto 36, 43
Murure 1–6, 8–14
terpenoids 173
Myrthaceae 202
Tharu communities 288–291, 293, 318, 319
therapeutic effects 219
N
Throreau 38
Ñamkulawen 91–93, 96 Tobas 187–194, 209, 211
native botanical 39 traditional knowledge 34–36, 45, 236, 237, 250
native medicinal plants 275, 276 traditional usage 227
Natural products 1, 3, 9
natural resource 211 V
Nepal 288–293, 318–320
Valerianaceae 90, 92, 96
nervous system 275, 276, 285
Verbenaceae 205, 208, 211
Nicotiana tabacum 205
vetiver oil 260, 261, 264, 266, 267, 270
Vetiveria zizanioides 255–257, 264–267, 270
O
Original Communities 191 Z
Ziziphus mistol 191, 203
Editors Biography