Secretory functions of the pancreas (choudhury) Flashcards

1
Q

what are the cells of the endocrine portion of the pancreas

A

islet cells of langerhan

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2
Q

what are the cells of the exocrine portion of the pancreas

A

acinar cells

duct cells

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3
Q

what do acinar cells secrete in the pancreas

A

pancreatic enzymes

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4
Q

what do duct cells in the pancreas secrete

A

aqueous NaHCO3- solution

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5
Q

what cells of the pancreas produce glucagon

A

alpha (A cells)

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6
Q

what cells of the pancreas produce insulin

A

Beta (B cells)

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7
Q

what cells of the pancreas produce somatostatin

A

D cells

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8
Q

what cells of the pancreas produce pancreatic polypeptide

A

pp cells

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9
Q

what is the effect of sympathetics on pancreas?

parasympathetics ?

A

inhibited by sympathetic &
-
stimulated by parasympathetic NS

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10
Q

what are the two ducts of the pancreas?

A

main pancreatic duct (Wirsung’s)

accessory collecting duct (Duct of Santorini)

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11
Q

what are the two components of exocrine secretions ?

A

aqueous bicarb component

enzymatic component

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12
Q

what stimulates the release of the aqueous component of the pancreatic juice

A

secretin

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13
Q

which factors stimulate acinar cells to secrete protein (enzymatic protein)

how do they increase the secretion?

A

ACh
CCK
Secretin
VIP

All increase intracellular Ca 2+ (second messenger) which helps vesicles fuse and release contents

Activation of protein kinases increases acinar cell secretion

all of this is to help digest fats, carbs and proteins that are in the duodenum

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14
Q

what is the composition of acinar cell fluid

A

isotonic

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15
Q

what are the effects of ACh and CCK on the acinar cells

A

stimulate NaCl secretion through phosphorylation of ion channels

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16
Q

what is the mechanism of action of secretin on ductal cells.

A

generates electrical gradient that favors Na HCO3- co-transport

(activates adenylyl cyclase, raises CAMP, stimulates protein kinase A and phosphorylates CFTR

17
Q

what are 6 enzymes in the acinar enzymatic secretions

A

amylase- carbohydrates
trypsinogen- proteins
lipase- triglycerides **very important only one lipase

procolipase (colipase)- removes the bile from the fat particles to make room for lipase to come in and break down the fat

trypsin inhibitors = protects against trypsin in acinar and ductal cells

glycoproteins = protects against protease (mediated mucosal immunity)

18
Q

how are pancreatic proteases activated

where is enterokinase located

A

enterokinase cleaves a hexapeptide from trypsinogen converting it to active enzyme trypsin

pancreatic proteases are secreted into the duodenum as inactive precursor

enterokinase is located in brush border of duodenal enterocytes (intestinal mucosal cells)

19
Q

what are the effects of CCK

A
coordinates GI activity (secretion) to food
 contracts gall bladder
 relaxes the sphincter of Oddi
 slows gastric motility 
 retards gastric emptying

the outcome of this is that there is matching of nutrient delivery to digestive and absorptive capacity

20
Q

what molecules stimulate CCK release

A

CCK-RP and MP which are both proteins

21
Q

what do GRP and ACh stimulate the release of

A

MP

22
Q

what is the signficance of peptide (protein) factors regulating CCK release

A

this is important so that CCK can inhibit its own release and doesn’t cause digestion of the lumen

23
Q

what cells release CCK

A

I cells

24
Q

what cells release secretin

A

s cells in duodenal mucosa

25
Q

at high rates of secretion what is the composition of pancreatic juice

A

alkaline

26
Q

what is achlorhydric. what is it caused by what can it lead to

A

Achlorhydric (unable to secrete gastric acid)
causes:
- secondary to disease
- on drugs, proton pump inhibitors,bicarbonate
fail to release secretin even in presence of a
fatty meal

leads to Duodenal ulcer b/c secretin levels are too low (not enough bicarb release)

27
Q

at what point do signs of malabsorption and indigestion appear

A

if pancreatic secretions fall below 10 percent

28
Q

what are two important causes of pancreatitis

A

alcohol (too many triglycerides and ca)

gallstones

29
Q

what is cystic fibrosis

what does this lead to

A

autosomal recessive genetic mutation in the CFTR Cl channel

Primarily affects caucasians
Lack chloride transporter at apical membrane
Leads to decreased water, HCO3, & Cl excretion, with concentration of protein in acinar ducts and blockage…. gland autodigestion/destruction
Progressive pulmonary and pancreatic insufficiency - chronic

30
Q

at low rates of pancreatic secretion what is the composition

A

na and cl dominate

31
Q

at high rates of pancreatic secretion what two molecules are predominate

A

Na and HCO3