T H E E N D O C R I N E S Y S T E M A N D C H E M I C A L
M E S S E N G E R S
B Y
NAVEED AKHTAR
ASSISTANT PROFESSOR OF ZOOLOGY
Communication III
Comparison of Nervous and Endocrine
System
Introduction
 The nervous and sensory systems work together to rapidly
communicate information and maintain homeostasis in an
animal’s body.
 In addition, many animals have a second, slower form of
communication and coordination—the endocrine system with
its chemical messengers.
 Evolution of Chemical Messenger:
 Some scientists suggest that chemical messengers may
initially have evolved in single-celled organisms to coordinate
feeding or reproduction.
 As multicellularity evolved, more complex organs also
evolved to govern the many individual coordination tasks, but
control centers relied on the same kinds of messengers that
were present in the simpler organisms.
 Chemical messengers have an ancient origin and must
have been conserved for hundreds of millions of years
 “old” messengers are adapted to new purposes. For
example, some ancient protein hormones are in species
ranging from bacteria to humans
 One key to the survival of any group of animals is proper
timing of activity so that growth, maturation, and
reproduction coincide with the times of year when
climate and food supply favor survival.
 It seems likely that the chemical messengers regulating
growth and reproduction were among the first to appear.
These messengers were probably secretions of neurons.
 .
 Later, specific hormones developed to play
important regulatory roles in molting, growth,
metamorphosis, and reproduction in various
invertebrates.
 Chemical messengers and their associated secretory
structures became even more complex with the
appearance of vertebrates
 A chemical messenger is a substance secreted by a cell or
tissue and it regulate activities of body functions.
 Types of Chemical Messengers:
 There are five major types of Chemical
messengers;
 1. Local Chemical Messenger (LCM)
 2. Neurotransmitters
 3. Neuropeptides
 4. Hormones
 5. Pheromones
 1. Local Chemical Messenger (LCM)
 Many cells secrete chemicals that alter physiological
conditions in the immediate vicinity
 Autocrine agents :Most of these chemicals act on
the same cell or adjacent cells
 Vertebrate examples include some of the chemicals
called lumones that the gut produces and that
help regulate digestion.
 In a wound, mast cells secrete a substance called
histamine that participates in the inflammatory
response.
 2. Neurotransmitters.
 neurons secrete chemicals called neurotransmitters
(e.g., nitric oxide and acetylcholine) that act on
immediately adjacent target cells
 These chemical messengers reach high
concentrations in the synaptic cleft, act quickly, and
are actively degraded and recycled.
 3. Neuropeptides or Neurohormones
 Some specialized neurons (called neurosecretory
cells) secrete neuropeptides (neurohormones).
 The blood or other body fluids transport
neuropeptides to nonadjacent target cells, where
neuropeptides exert their effects
 In mammals, for example, certain nerve cells in the
hypothalamus release a neuropeptide that causes the
pituitary gland to release the hormone oxytocin,
which induces powerful uterine contractions during
the delivery of offspring.
 4. Hormones
 Secretions of endocrine glands that are released into
the blood to be transported to a target organ to show
its effect.
 Example : Insulin
 5. Pheromones.
 Pheromones are chemical messengers released to the
exterior of one animal that affect the behavior of
another individual of the same species
The Endocrine System and Chemical Messengers
The Endocrine System and Chemical Messengers
How do hormones and neurotransmitters differ?
HORMONES AND THEIR FEEDBACK
SYSTEMS
 What are hormones?
 A hormone (Gr. hormaein, to set in motion or to spur
on) is a specialized chemical messenger that an
endocrine gland or tissue produces and secretes.
 Hormones circulate through body fluids and affect
the metabolic activity of a target cell or tissue in a
specific way.
 By definition, a target cell has receptors to which
chemical messengers either selectively bind or on
which they have an effect
 Endocrinology :The study of endocrine glands and
their hormones is called endocrinology
 Biochemistry of Hormones:
 Amount of Hormones:
 Hormones are effective in extremely small amounts.
 Only a few molecules of a hormone may be enough to produce
a dramatic response in a target cell. In the target cell
 Working of Hormones:
 Hormones influence cellular functions byaltering rates of
biochemical processes intarget cells
 Change membrane permeability to increase or decrease the
diffusion rate of a substance
 Affect enzyme synthesis and activity to alter cell metabolism
 Stimulate release of hormones from other glands
 This is a dynamic process that must be regulated, not just
activated
Feedback Control System of Hormone
Secretion
The Endocrine System and Chemical Messengers
Hormonal Feedback
MECHANISMS OF HORMONE ACTION
 Hormones modify the biochemical activity of a target cell or
tissue.
 Two basic mechanisms are involved.
 The first, the fixed-membrane-receptor mechanism,
applies to hormones that are proteins or amines
 Because they are water soluble (hydrophilic) and cannot
diffuse across the plasma membrane, these hormones initiate
their response by means of specialized receptors on the
plasma membrane of the target cell.
 The second, the mobile-receptor mechanism, applies to
steroid hormones.
 These hormones are lipid soluble (lipophilic) and diffuse
easily into the cytoplasm, where they initiate their response by
binding to cytoplasmic receptors
The Endocrine System and Chemical Messengers
Fixed-Membrane-Receptor Mechanism
Mobile-Receptor Mechanism
SOME HORMONES OF INVERTEBRATES
 The first hormones were probably neurosecretions.
 1. Porifera
 The porifera (sponges) do not have classical endocrine
glands. Because sponges do not have neurons, they also
do not have neurosecretory cells
 2. Cnidarians
 The nerve cells of Hydra contain a growth-promoting
hormone that stimulates budding, regeneration, and
growth.
 For example, when the hormone is present in the
medium in which fragments of Hydra are incubated,
“head” regeneration is accelerated. This so-called “head
activator” also stimulates mitosis in Hydra.
 3. Platyhelminthes
 Neurosecretary Cells
 Cerebral ganglion
 Neuropeptides: regeneration, asexual reproduction, and
gonad maturation
 Example: neurosecretory cells in the scolex of some
tapeworms control shedding of the proglottids
 4. Nemerteans
 Nemerteans have more cephalization than
platyhelminthes and a larger brain, composed of a dorsal and
ventral pair of ganglia connected by a nerve ring.
 The neuropeptide that these ganglia produce appears to
control gonadal development and regulate water balance
 5. Nematodes
 No classical endocrine system
 Only neurosecretory cells
 Control ecdysis or moulting
 The neuropeptide is released after a new cuticle is
produced and stimulates the excretory gland to
secrete an enzyme (leucine aminopeptidase) into
the space between the old and new cuticles. The
accumulation of fluid in this space causes the old
cuticle to split and be shed
 6. Molluscs
 The ring of ganglia that constitutes the central
nervous system of molluscs is richly endowed with
neurosecretory cells.
 The neuropeptides that these cells produce help
regulate heart rate, kidney function, and
energy metabolism. The intestines of some
bivalves have been found to produce insulin,
which may have a carbohydrate-regulating role
similar to that of insulin in vertebrates
 In certain gastropods, such as the common land snail
Helix, a specific hormone stimulates spermatogenesis;
another hormone, termed egg-laying hormone,
stimulates egg development; and hormones from the
ovary and testis stimulate accessory sex organs.
 In all snails, a growth hormone controls shell growth
 In cephalopods, such as the octopus and squid, the
optic gland in the eyestalk produces one or more
hormones that stimulate egg development, proliferation
of spermatogonia, and the development of secondary
sexual characterists
 7. Annelids
 A well-developed and cephalized nervous system, a
well-developed circulatory system, and a large
coelom demands well developed endocrine system
 The various endocrine systems of annelids are
generally involved with morphogenesis,
development, growth, regeneration, and gonadal
maturation.
 For example, in polychaetes, juvenile hormone
inhibits the gonads and stimulates growth and
regeneration
 Another hormone, gonadotropin, stimulates the
development of eggs, whereas the hormone
annetocin (related to vertebrate oxytocin) elicits
egg-laying behavior.
 In leeches, a neuropeptide stimulates gamete
development and triggers color changes.
Osmoregulatory hormones have been reported in
oligochaetes, and a hyperglycemic hormone that
maintains a high concentration of blood glucose has
been reported for the oligochaete Lumbricus.
 8. Arthropods:
 The endocrine systems of crustaceans and insects
are excellent examples of how hormones regulate
growth, maturation, and reproduction.
 Much is known about hormones and their
functioning in these animals
 The endocrine system of a crustacean, such as a
crayfish, controls functions such as ecdysis
(molting), sex determination, and color changes.
 X-Organ: X-organs are neurosecretory tissues in the
crayfish eyestalks
 Associated with each X-organ is a sinus gland that
accumulates and releases the secretions of the X-organ.
 Y -Organ:
 Other glands, called Y-organs, are at the base of the
maxillae
 Mechanism of Ecdysis:
 X-organs and Y-organs control ecdysis as follows. In the
absence of an appropriate stimulus, the X-organ
produces molt-inhibiting hormone (MIH), and the
sinus gland releases
Control of Ecdysis (Molting) in
Crustaceans.
Control of Ecdysis (Molting) in
Crustaceans.
 The target of this hormone is the Y-organ. When
MIH is present in high concentrations, the Y-organ is
inactive.
 Under appropriate internal and external stimuli,
MIH release is prevented, and the Y-organ releases
the hormone ecdysone, which leads to molting
Control of Ecdysis (Molting) and
Development (Metamorphosis) in an Insect.
 The sequence of events in insects is similar to that of
crustaceans, but it does not involve a molt-inhibiting
hormone.
 The presence of an appropriate stimulus to the central
nervous system activates certain neurosecretory cells (pars
intercerebralis) in the optic lobes of the brain
 These cells secrete the hormone ecdysiotropin, which
axons transport to the corpora cardiaca (a mass of
neurons associated with the brain). The corpora
cardiaca produces thoracotropic hormone, which is
carried to the prothoracic glands, stimulating them to
produce and release ecdysone, which induces molting —in
particular, the reabsorption of some of the old cuticle and the
development of a new cuticle.
 Bursicon Hormone:
 Other neurosecretory cells in the brain and nerve
cords produce the hormone bursicon. Bursicon
influences certain aspects of epidermal development,
such as tanning (i.e., hardening and darkening of the
chitinous outer cuticle layer).
 Tanning is completed several hours after each
molting.
The Endocrine System and Chemical Messengers
The Endocrine System and Chemical Messengers
 Juvenile hormone (JH):
 Another hormone, juvenile hormone (JH), is also involved in
the morphological differentiation that occurs during the
molting of insects.
 Just behind the insect brain are the paired corpora allata
 These structures produce JH. High concentrations of JH in
the blood of an insect inhibit differentiation. In the absence of
an appropriate environmental stimulus, the corpora allata
decrease JH production, which causes the insect larva to
differentiate into a pupa.
 The pupa then forms a cocoon to overwinter. In the spring, a
final surge of ecdysone, in the absence of JH, transforms the
pupa into an adult moth.
 9: Echinoderms:
 Because echinoderms are deuterostomes, they are more closely
allied with chordates than the other invertebrates.
 However, the endocrine systems of echinoderms provide few
insights into the evolution of chordate endocrine systems, because
echinoderm hormones and endocrine glands are very different from
those of chordates.
 the radial nerves of sea stars contain a neuropeptide called
gonad-stimulating substance. When this neuropeptide is
injected into a mature sea star, it induces immediate shedding of the
gametes, spawning behavior, and meiosis in the oocytes.
 The neuropeptide also causes the release of a hormone called
maturationinducing substance, which has various effects on
the reproductive system
The Endocrine System and Chemical Messengers
AN OVERVIEW OF THE
VERTEBRATE
ENDOCRINE SYSTEM

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The Endocrine System and Chemical Messengers

  • 1. T H E E N D O C R I N E S Y S T E M A N D C H E M I C A L M E S S E N G E R S B Y NAVEED AKHTAR ASSISTANT PROFESSOR OF ZOOLOGY Communication III
  • 2. Comparison of Nervous and Endocrine System
  • 3. Introduction  The nervous and sensory systems work together to rapidly communicate information and maintain homeostasis in an animal’s body.  In addition, many animals have a second, slower form of communication and coordination—the endocrine system with its chemical messengers.  Evolution of Chemical Messenger:  Some scientists suggest that chemical messengers may initially have evolved in single-celled organisms to coordinate feeding or reproduction.  As multicellularity evolved, more complex organs also evolved to govern the many individual coordination tasks, but control centers relied on the same kinds of messengers that were present in the simpler organisms.
  • 4.  Chemical messengers have an ancient origin and must have been conserved for hundreds of millions of years  “old” messengers are adapted to new purposes. For example, some ancient protein hormones are in species ranging from bacteria to humans  One key to the survival of any group of animals is proper timing of activity so that growth, maturation, and reproduction coincide with the times of year when climate and food supply favor survival.  It seems likely that the chemical messengers regulating growth and reproduction were among the first to appear. These messengers were probably secretions of neurons.  .
  • 5.  Later, specific hormones developed to play important regulatory roles in molting, growth, metamorphosis, and reproduction in various invertebrates.  Chemical messengers and their associated secretory structures became even more complex with the appearance of vertebrates
  • 6.  A chemical messenger is a substance secreted by a cell or tissue and it regulate activities of body functions.  Types of Chemical Messengers:  There are five major types of Chemical messengers;  1. Local Chemical Messenger (LCM)  2. Neurotransmitters  3. Neuropeptides  4. Hormones  5. Pheromones
  • 7.  1. Local Chemical Messenger (LCM)  Many cells secrete chemicals that alter physiological conditions in the immediate vicinity  Autocrine agents :Most of these chemicals act on the same cell or adjacent cells  Vertebrate examples include some of the chemicals called lumones that the gut produces and that help regulate digestion.  In a wound, mast cells secrete a substance called histamine that participates in the inflammatory response.
  • 8.  2. Neurotransmitters.  neurons secrete chemicals called neurotransmitters (e.g., nitric oxide and acetylcholine) that act on immediately adjacent target cells  These chemical messengers reach high concentrations in the synaptic cleft, act quickly, and are actively degraded and recycled.
  • 9.  3. Neuropeptides or Neurohormones  Some specialized neurons (called neurosecretory cells) secrete neuropeptides (neurohormones).  The blood or other body fluids transport neuropeptides to nonadjacent target cells, where neuropeptides exert their effects  In mammals, for example, certain nerve cells in the hypothalamus release a neuropeptide that causes the pituitary gland to release the hormone oxytocin, which induces powerful uterine contractions during the delivery of offspring.
  • 10.  4. Hormones  Secretions of endocrine glands that are released into the blood to be transported to a target organ to show its effect.  Example : Insulin  5. Pheromones.  Pheromones are chemical messengers released to the exterior of one animal that affect the behavior of another individual of the same species
  • 13. How do hormones and neurotransmitters differ?
  • 14. HORMONES AND THEIR FEEDBACK SYSTEMS  What are hormones?  A hormone (Gr. hormaein, to set in motion or to spur on) is a specialized chemical messenger that an endocrine gland or tissue produces and secretes.  Hormones circulate through body fluids and affect the metabolic activity of a target cell or tissue in a specific way.  By definition, a target cell has receptors to which chemical messengers either selectively bind or on which they have an effect
  • 15.  Endocrinology :The study of endocrine glands and their hormones is called endocrinology  Biochemistry of Hormones:
  • 16.  Amount of Hormones:  Hormones are effective in extremely small amounts.  Only a few molecules of a hormone may be enough to produce a dramatic response in a target cell. In the target cell  Working of Hormones:  Hormones influence cellular functions byaltering rates of biochemical processes intarget cells  Change membrane permeability to increase or decrease the diffusion rate of a substance  Affect enzyme synthesis and activity to alter cell metabolism  Stimulate release of hormones from other glands  This is a dynamic process that must be regulated, not just activated
  • 17. Feedback Control System of Hormone Secretion
  • 20. MECHANISMS OF HORMONE ACTION  Hormones modify the biochemical activity of a target cell or tissue.  Two basic mechanisms are involved.  The first, the fixed-membrane-receptor mechanism, applies to hormones that are proteins or amines  Because they are water soluble (hydrophilic) and cannot diffuse across the plasma membrane, these hormones initiate their response by means of specialized receptors on the plasma membrane of the target cell.  The second, the mobile-receptor mechanism, applies to steroid hormones.  These hormones are lipid soluble (lipophilic) and diffuse easily into the cytoplasm, where they initiate their response by binding to cytoplasmic receptors
  • 24. SOME HORMONES OF INVERTEBRATES
  • 25.  The first hormones were probably neurosecretions.  1. Porifera  The porifera (sponges) do not have classical endocrine glands. Because sponges do not have neurons, they also do not have neurosecretory cells  2. Cnidarians  The nerve cells of Hydra contain a growth-promoting hormone that stimulates budding, regeneration, and growth.  For example, when the hormone is present in the medium in which fragments of Hydra are incubated, “head” regeneration is accelerated. This so-called “head activator” also stimulates mitosis in Hydra.
  • 26.  3. Platyhelminthes  Neurosecretary Cells  Cerebral ganglion  Neuropeptides: regeneration, asexual reproduction, and gonad maturation  Example: neurosecretory cells in the scolex of some tapeworms control shedding of the proglottids  4. Nemerteans  Nemerteans have more cephalization than platyhelminthes and a larger brain, composed of a dorsal and ventral pair of ganglia connected by a nerve ring.  The neuropeptide that these ganglia produce appears to control gonadal development and regulate water balance
  • 27.  5. Nematodes  No classical endocrine system  Only neurosecretory cells  Control ecdysis or moulting  The neuropeptide is released after a new cuticle is produced and stimulates the excretory gland to secrete an enzyme (leucine aminopeptidase) into the space between the old and new cuticles. The accumulation of fluid in this space causes the old cuticle to split and be shed
  • 28.  6. Molluscs  The ring of ganglia that constitutes the central nervous system of molluscs is richly endowed with neurosecretory cells.  The neuropeptides that these cells produce help regulate heart rate, kidney function, and energy metabolism. The intestines of some bivalves have been found to produce insulin, which may have a carbohydrate-regulating role similar to that of insulin in vertebrates
  • 29.  In certain gastropods, such as the common land snail Helix, a specific hormone stimulates spermatogenesis; another hormone, termed egg-laying hormone, stimulates egg development; and hormones from the ovary and testis stimulate accessory sex organs.  In all snails, a growth hormone controls shell growth  In cephalopods, such as the octopus and squid, the optic gland in the eyestalk produces one or more hormones that stimulate egg development, proliferation of spermatogonia, and the development of secondary sexual characterists
  • 30.  7. Annelids  A well-developed and cephalized nervous system, a well-developed circulatory system, and a large coelom demands well developed endocrine system  The various endocrine systems of annelids are generally involved with morphogenesis, development, growth, regeneration, and gonadal maturation.  For example, in polychaetes, juvenile hormone inhibits the gonads and stimulates growth and regeneration
  • 31.  Another hormone, gonadotropin, stimulates the development of eggs, whereas the hormone annetocin (related to vertebrate oxytocin) elicits egg-laying behavior.  In leeches, a neuropeptide stimulates gamete development and triggers color changes. Osmoregulatory hormones have been reported in oligochaetes, and a hyperglycemic hormone that maintains a high concentration of blood glucose has been reported for the oligochaete Lumbricus.
  • 32.  8. Arthropods:  The endocrine systems of crustaceans and insects are excellent examples of how hormones regulate growth, maturation, and reproduction.  Much is known about hormones and their functioning in these animals  The endocrine system of a crustacean, such as a crayfish, controls functions such as ecdysis (molting), sex determination, and color changes.
  • 33.  X-Organ: X-organs are neurosecretory tissues in the crayfish eyestalks  Associated with each X-organ is a sinus gland that accumulates and releases the secretions of the X-organ.  Y -Organ:  Other glands, called Y-organs, are at the base of the maxillae  Mechanism of Ecdysis:  X-organs and Y-organs control ecdysis as follows. In the absence of an appropriate stimulus, the X-organ produces molt-inhibiting hormone (MIH), and the sinus gland releases
  • 34. Control of Ecdysis (Molting) in Crustaceans.
  • 35. Control of Ecdysis (Molting) in Crustaceans.
  • 36.  The target of this hormone is the Y-organ. When MIH is present in high concentrations, the Y-organ is inactive.  Under appropriate internal and external stimuli, MIH release is prevented, and the Y-organ releases the hormone ecdysone, which leads to molting
  • 37. Control of Ecdysis (Molting) and Development (Metamorphosis) in an Insect.  The sequence of events in insects is similar to that of crustaceans, but it does not involve a molt-inhibiting hormone.  The presence of an appropriate stimulus to the central nervous system activates certain neurosecretory cells (pars intercerebralis) in the optic lobes of the brain  These cells secrete the hormone ecdysiotropin, which axons transport to the corpora cardiaca (a mass of neurons associated with the brain). The corpora cardiaca produces thoracotropic hormone, which is carried to the prothoracic glands, stimulating them to produce and release ecdysone, which induces molting —in particular, the reabsorption of some of the old cuticle and the development of a new cuticle.
  • 38.  Bursicon Hormone:  Other neurosecretory cells in the brain and nerve cords produce the hormone bursicon. Bursicon influences certain aspects of epidermal development, such as tanning (i.e., hardening and darkening of the chitinous outer cuticle layer).  Tanning is completed several hours after each molting.
  • 41.  Juvenile hormone (JH):  Another hormone, juvenile hormone (JH), is also involved in the morphological differentiation that occurs during the molting of insects.  Just behind the insect brain are the paired corpora allata  These structures produce JH. High concentrations of JH in the blood of an insect inhibit differentiation. In the absence of an appropriate environmental stimulus, the corpora allata decrease JH production, which causes the insect larva to differentiate into a pupa.  The pupa then forms a cocoon to overwinter. In the spring, a final surge of ecdysone, in the absence of JH, transforms the pupa into an adult moth.
  • 42.  9: Echinoderms:  Because echinoderms are deuterostomes, they are more closely allied with chordates than the other invertebrates.  However, the endocrine systems of echinoderms provide few insights into the evolution of chordate endocrine systems, because echinoderm hormones and endocrine glands are very different from those of chordates.  the radial nerves of sea stars contain a neuropeptide called gonad-stimulating substance. When this neuropeptide is injected into a mature sea star, it induces immediate shedding of the gametes, spawning behavior, and meiosis in the oocytes.  The neuropeptide also causes the release of a hormone called maturationinducing substance, which has various effects on the reproductive system
  • 44. AN OVERVIEW OF THE VERTEBRATE ENDOCRINE SYSTEM