GI Tract Secretions Flashcards

1
Q

What are the 3 regulatory phases of GI function?

A
  1. cephalic
  2. gastric
  3. intestinal
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2
Q

What are the primary regulatory events in the cephalic phase?

A
  • initiated by taste/smell of food
  • vagal activity triggers increase in salivary secretions
  • increase in stomach secretions (HCl, pepsin, mucus and gastrin)
  • stimulates bile ducts, hepatocytes and pancreatic acinar cells
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3
Q

What are the primary regulatory events in the gastric phase?

A
  • initiated by food entering stomach causing distension and release of gastrin
  • G cells triggered by parasympathetic pathways
  • decreased acidity in stomach from buffering of food
  • distension of antrum
  • breakdown products of gastrin (amino acids, peptides and proteins)
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4
Q

What are the primary regulatory events in the intestinal phase?

A
  • initiated by presence of food in duodenum
  • if pH below 2: gastric inhibition and intestinal stimulation
  • if pH above 3: release of gastrin, acid causes release of secretin
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5
Q

What factors affect saliva secretion?

A
  • sympathetic and parasympathetic NS increase saliva secretion:
  • PSNS: produce large volume of watery, enzyme rich saliva
  • SNS: produce small volume, thick, mucousy saliva
  • sleep, dehydration and atropine decrease saliva secretion
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6
Q

Describe the process of saliva release

A
  • acinar cells secrete primary secretions containing Na, Cl, K, bicarbonate, amylase and mucin
  • myoepithelial cells are stimulated to eject saliva
  • ductal cells cause secondary modification (resorbs Na, Cl and adds K)
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7
Q

How does flow rate affect bicarbonate concentration of saliva?

A
  • high flow rate = high bicarbonate concentration

- so after a meal, bicarbonate can protect teeth from bacteria

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8
Q

What are the different salivation reflexes?

A
  • simple: pressure receptors in mouth activated in presence of food
  • acquired: smell/see/hear in preparation of meal
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9
Q

How does the oesophagus produce secretions?

A
  • the main body is lined by simple mucous glands for mechanical damage protection
  • gastric end has compound mucus glands to protect against chemical damage
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10
Q

Where are the different cell types found in the stomach?

A
  • body: parietal and chief cells

- antrum: G cells and mucous cells

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11
Q

What are the different gastric secretions and their functions?

A
  • HCL: small protein digestion and activation of pepsinogen
  • pepsinogen: protein digestion
  • intrinsic factor: vitamin B absorption
  • mucous: protection and lubrication
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12
Q

What increases the surface area of the stomach?

A
  • gastric pits that contain mucous cells, parietal and chief cells
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13
Q

When is HCl secreted and describe its process

A
  • to protect parietal cells
  • at basolateral membrane, bicarbonate ions exchanged for Cl-
  • at apical membrane H+ are secreted into lumen by H/K-ATPase and Cl- ions then diffuse across membrane
  • in the lumen they form HCl
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14
Q

What are the proportions of secretions that occur at each gastric stage?

A
  • cephalic: 30% by stimulation of parietal cells by vagus directly or gastrin indirectly
  • gastric: 60% by vagal stimulation direct by distension or local reflexes that cause gastrin release
  • intestinal: 10% from presence of breakdown products
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15
Q

What is HCl secretion inhibited and how?

A
  • when HCl is no longer needed to convert pepsinogen into pepsin
  • somatostatin directly inhibits release by binding to receptors on parietal cells
  • inhibiting histamine or gastrin release indirectly inhibits it
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16
Q

How is pepsinogen secreted?

A
  • by chief and mucous cells in oxynitic glands in response to vagal stimulation
  • H+ ions trigger local reflexes that stimulate secretion
17
Q

What makes up exocrine pancreatic secretions and what are its functions?

A
  • made up of solution of enzymes and bicarbonate ions
  • bicarbonate ions neutralise stoamch acid
  • enzymes digest carbs, proteins, lipis
18
Q

What increases exocrine pancreas secretions?

A
  • secretin
  • CCK
  • parasympathetic NS
19
Q

How are pancreatic secretions formed?

A
  • aqueous component released from centroacinar and ductal cells
  • ductal cells cause high bicarbonate content
  • acinar cells release enzymes
  • amylase and lipase are active
  • protease is inactive and needs activation in duodenum
20
Q

What are the 3 major proteolytic enzymes?

A
  • trypsinogen
  • chymotrypsinogen
  • procarboxypeptidase
  • allinactive in zymogen cells to prevent self digestion
21
Q

How are the proteolytic enzymes activated?

A
  • trypsinogen activated by enterokinase/enteropeptidase to form trypsin
  • trypsin then activates more trypsinogen
  • chymotrypsinogen to form chymotrypsin
  • and procarboxypeptidase to form carboxypeptidase
22
Q

How does the pancreas respond to the intestinal phase of digestion?

A
  • duodenal I cells secrete CCK, vagal release of ACh potentiates CCK action
  • triggers acinar cells to produce enzymes
  • secretin stimulus for bicarbonate secretion
  • CCK and ACh potentiate secretion action
  • triggers ductal cells to produce Na, K, Cl and HCO
23
Q

What is the function of the gallbladder?

A
  • stores bile produced by hepatocytes
  • concentrates bile
  • CCK major stimulus for bile ejection (released from I cells in duodenum and jejunum)
24
Q

Describe the regulation of bile secretion

A
  • between meals: bile salts recirculate to liver so more bile produced then stored in gallbladder
  • cephalic phase: vagal stimulation increases bile flow
  • after meal: chyme in duodenum stimulates release of CCK and secretin (triggers bile release)
25
Q

Describe the secretions of the small intestine

A
  • crypts of leiberkuhn and villi are covered in goblet cells (release mucus) and enterocytes that secrete water and electrolytes
  • secrete water and electrolytes in crypts
  • absorbs water and electrolytes in the villi
  • secretions regulated by distension and irritative/tactile stimuli from chyme
26
Q

Describe the secretions of the large intestines

A
  • alkaline mucus high in potassium and bicarbonate
  • protects and lubricates and neutralises H+ ions produced by gut bacteria
  • secretion stimulated by distension and some parasympathetic input