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Gastrointestinal Peptides
Presented By Trishna Kisiju
Introduction
• Signaling molecules released from the
enteroendocrine cells or gastrointestinal
neurons.
Characteristics of GI peptides
• Water and electrolyte secretion
• Enzyme secretion
• Contraction and relaxation of the smooth muscle
• Regulate the release of other endocrines
• Have trophic effects
Classification of GI peptides
GI Peptides
Hormones Paracrines Neurocrines
Fig: Classification of gastrointestinal peptides as hormones,
paracrines or neurocrines. GI, Gastrointestinal; R, Receptor.
Hormones
• Greek : ‘‘to set in motion’’
• Major GI hormones:
i) Secretin
ii) Gastrin
iii) Cholecystokinin- Pancreozymine (CCK-PZ)
iv) Gastric inhibitory peptide (GIP)
v) Motilin
• Some criteria must be satisfied to prove the
existence of a GI hormone:
(1) Substance must be secreted in response to a
physiologic stimulus and be carried in the
bloodstream to a distant site, where it produces
a physiologic action.
(2) Function must be independent of any neural
activity.
Criteria contd..
(3) Must be isolated, purified, identified
chemically, and synthesized in vitro.
Major types of GI hormones
Figure: Principal sites of gastrointestinal hormone release.
• CCK: Cholecystokinin
• GIP: Glucose dependent insulinotropic peptide
Gastrin
• Source: G cells, mainly in antral region.
• Types: Two types of gastrin physiologically
important:
G34: big gastrin, found in the interdigestive state.
G17: little gastrin; accounts for about 90% of the gastrin
found in antral mucosa.
• Stimulus: Products of protein digestion, distention
of the stomach by food and vagal stimulation
• Metabolism: t1/2 of G34 = 38 minutes
t1/2 of G17 = 7 minutes
Gastrin contd..
• Mechanism of action:
P= Pepsinogen, SST= Somatostatin, GRP= Gastrin Releasing Peptide
Gastrin contd..
• Functions:
1. Stimulation of gastric acid secretion from parietal cells
and pepsin secretion.
(Therefore, hypergastrinemia causes peptic ulcer.)
2. Trophic action of gastrin.
3. Stimulates gastric motility and exocrine pancreas
secretion.
4. Prevents reflux esophagitis.
Functions contd..
5. Stimulates insulin secretion.
6. Causes colonic contraction that initiates
gastrocolic reflex after a meal.
7. Stimulates histamine secretion from ECL
(enterochromaffin like cells) in GI mucosa.
Regulation of Gastrin Secretion
Cholecystokinin
• Source: I cells in the mucosa of upper small
intestine.
• Stimulus: Fatty acids, monoglycerides, peptides
and amino acids.
• Metabolism: t1/2 = 5 minutes
• Functions of CCK:
1. Stimulates contraction of gallbladder.
2. Stimulates pancreatic secretion rich in enzymes.
Therefore, CCK is also called cholecystokinin-pancreozymin (CCK-
PZ).
3. Inhibits gastric acid secretion.
4. Inhibits gastric motility, thereby delays gastric
emptying.
5. Causes relaxation of sphincter of Oddi.
Functions of CCK
6. Stimulates growth of exocrine pancreas and gall
bladder.
7. Augments (increases) contraction of pyloric
sphincter.
8. Stimulates glucagon secretion.
9. In brain, acts as an anorexigenic neurotransmitter.
Regulation of CCK secretion
Secretin
• Source: S cells of Duodenum.
• Stimuli: Acid and fats.
• Functions:
1. Increases secretion of pancreatic juice rich in
bicarbonate and bile secretion.
2. Inhibits effects of gastrin on parietal cells.
3. Decreases gastric acid secretion and motility.
Glucose-dependent insulinotropic
polypeptide (GIP)
• Also known as Gastric Inhibitory Peptide
• Source: K cells present in the mucosa of duodenum
and jejunum.
• Stimuli: Carbs, fatty acids and peptides
• Functions:
1. It inhibits gastric secretion and motility.
2. It stimulates insulin secretion.
• Regulation of GIP secretion:
- Secretion is increased by glucose and fat in the
duodenum.
Motilin
• Source: Mo cells
• Released approximately every 90 min during
fasting.
• Functions:
1. Increases GI motility, especially in the
interdigestive phase.
2. Major regulator of migrating motor complex
(MMC).
Candidate Hormones
• Fail to meet one or more criteria to be called an
official GI hormone.
Paracrines
• Synthesized in the endocrine cells of the GI tract.
• Do not enter the systemic circulation
• Act locally, reaching their target cells by diffusing
over short distances.
Neurocrines
• Synthesized in cell bodies of gastrointestinal
neurons.
• Action potential in the neuron
Causes release of the neurocrine that diffuses
across the synapse
Interacts with receptors on the postsynaptic cell
Major Neurocrines
THANK YOU!!!
References
• Harvey, Richard A., Ph. D. (2011). Lippincott's
illustrated reviews: Biochemistry. Philadelphia :
Wolters Kluwer Health, Pg 379-381.
• Costanzo, L. S. (2011). Physiology. Philadelphia:
Wolters Kluwer Health/Lippincott Williams &
Wilkins, Pg 342-348
• Johnson Leonard R.(2003). Essential Medical
Physioogy. San Diego, California : Elsevier, Pg
468-476

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Gastrointestinal peptides

  • 2. Introduction • Signaling molecules released from the enteroendocrine cells or gastrointestinal neurons.
  • 3. Characteristics of GI peptides • Water and electrolyte secretion • Enzyme secretion • Contraction and relaxation of the smooth muscle • Regulate the release of other endocrines • Have trophic effects
  • 4. Classification of GI peptides GI Peptides Hormones Paracrines Neurocrines
  • 5. Fig: Classification of gastrointestinal peptides as hormones, paracrines or neurocrines. GI, Gastrointestinal; R, Receptor.
  • 6. Hormones • Greek : ‘‘to set in motion’’ • Major GI hormones: i) Secretin ii) Gastrin iii) Cholecystokinin- Pancreozymine (CCK-PZ) iv) Gastric inhibitory peptide (GIP) v) Motilin
  • 7. • Some criteria must be satisfied to prove the existence of a GI hormone: (1) Substance must be secreted in response to a physiologic stimulus and be carried in the bloodstream to a distant site, where it produces a physiologic action. (2) Function must be independent of any neural activity.
  • 8. Criteria contd.. (3) Must be isolated, purified, identified chemically, and synthesized in vitro.
  • 9. Major types of GI hormones
  • 10. Figure: Principal sites of gastrointestinal hormone release. • CCK: Cholecystokinin • GIP: Glucose dependent insulinotropic peptide
  • 11. Gastrin • Source: G cells, mainly in antral region. • Types: Two types of gastrin physiologically important: G34: big gastrin, found in the interdigestive state. G17: little gastrin; accounts for about 90% of the gastrin found in antral mucosa. • Stimulus: Products of protein digestion, distention of the stomach by food and vagal stimulation • Metabolism: t1/2 of G34 = 38 minutes t1/2 of G17 = 7 minutes
  • 12. Gastrin contd.. • Mechanism of action: P= Pepsinogen, SST= Somatostatin, GRP= Gastrin Releasing Peptide
  • 13. Gastrin contd.. • Functions: 1. Stimulation of gastric acid secretion from parietal cells and pepsin secretion. (Therefore, hypergastrinemia causes peptic ulcer.) 2. Trophic action of gastrin. 3. Stimulates gastric motility and exocrine pancreas secretion. 4. Prevents reflux esophagitis.
  • 14. Functions contd.. 5. Stimulates insulin secretion. 6. Causes colonic contraction that initiates gastrocolic reflex after a meal. 7. Stimulates histamine secretion from ECL (enterochromaffin like cells) in GI mucosa.
  • 16. Cholecystokinin • Source: I cells in the mucosa of upper small intestine. • Stimulus: Fatty acids, monoglycerides, peptides and amino acids. • Metabolism: t1/2 = 5 minutes
  • 17. • Functions of CCK: 1. Stimulates contraction of gallbladder. 2. Stimulates pancreatic secretion rich in enzymes. Therefore, CCK is also called cholecystokinin-pancreozymin (CCK- PZ). 3. Inhibits gastric acid secretion. 4. Inhibits gastric motility, thereby delays gastric emptying. 5. Causes relaxation of sphincter of Oddi.
  • 18. Functions of CCK 6. Stimulates growth of exocrine pancreas and gall bladder. 7. Augments (increases) contraction of pyloric sphincter. 8. Stimulates glucagon secretion. 9. In brain, acts as an anorexigenic neurotransmitter.
  • 19. Regulation of CCK secretion
  • 20. Secretin • Source: S cells of Duodenum. • Stimuli: Acid and fats. • Functions: 1. Increases secretion of pancreatic juice rich in bicarbonate and bile secretion. 2. Inhibits effects of gastrin on parietal cells. 3. Decreases gastric acid secretion and motility.
  • 21. Glucose-dependent insulinotropic polypeptide (GIP) • Also known as Gastric Inhibitory Peptide • Source: K cells present in the mucosa of duodenum and jejunum. • Stimuli: Carbs, fatty acids and peptides • Functions: 1. It inhibits gastric secretion and motility. 2. It stimulates insulin secretion. • Regulation of GIP secretion: - Secretion is increased by glucose and fat in the duodenum.
  • 22. Motilin • Source: Mo cells • Released approximately every 90 min during fasting. • Functions: 1. Increases GI motility, especially in the interdigestive phase. 2. Major regulator of migrating motor complex (MMC).
  • 23. Candidate Hormones • Fail to meet one or more criteria to be called an official GI hormone.
  • 24. Paracrines • Synthesized in the endocrine cells of the GI tract. • Do not enter the systemic circulation • Act locally, reaching their target cells by diffusing over short distances.
  • 25. Neurocrines • Synthesized in cell bodies of gastrointestinal neurons. • Action potential in the neuron Causes release of the neurocrine that diffuses across the synapse Interacts with receptors on the postsynaptic cell
  • 28. References • Harvey, Richard A., Ph. D. (2011). Lippincott's illustrated reviews: Biochemistry. Philadelphia : Wolters Kluwer Health, Pg 379-381. • Costanzo, L. S. (2011). Physiology. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins, Pg 342-348 • Johnson Leonard R.(2003). Essential Medical Physioogy. San Diego, California : Elsevier, Pg 468-476