Cell Types And Function Flashcards
What is the function of G cells, what do they secrete and from where?
Secrete Gastrin - found in Antrum of stomach and duodenum
What is the function of I cells, what do they secrete and from where?
They secrete CCK - found in duodenum and jejunum
What is the function of S cells, what do they secrete and from where?
Secrete Secretin - duodenum
What is the function of D cells, what do they secrete and from where?
Secrete Somatostatin- pancreatic islets and GI mucosa
What is the function of Gastric parietal cells, what do they secrete?
Secrete Gastric acid and Intrinsic Factor
What hormones stimulate pancreatic secretion?
CCK - stim. both the pancreas and gallbladder (I cells)
Secretin- stimulates bicarbonate secretion (S cells)
Not hormone:
Acetylcholine from CN X - vagus nerve
What enzyme catalyzes the rate-limiting step in carbohydrate digestion?
Oligosaccharide hydrolases found at the intestinal brush border
An alcoholic patient diagnosed with alcoholic hepatitis receives lab values with increased AST/ALT. What is the hallmark feature of this disease in terms of lab ratios, and why is one different from the other?
AST is 2x higher to ALT, and this is because alcohol depleted levels of ALT due to B6 deficiency seen in alcohol metabolism.
“A Scotch and Tonic”
If hepatocytes can no longer metabolize toxins and ammonia, what pathology is at hand with the following clinical features:
-confusion, delirium, and hypersomnia
-coma, death
-Asterixis: Px extends arms + wrists out, and hands begin to flap, bc they can’t maintain wrist extension.
-Fetor hepaticus (musty odor): aka breath of death
What is the treatment as well?
Hepatic encephalopathy
Tx- Diuretics, beta-blockers (nadol or propranolol), Vitamin K, and lactulose
What defect causing pathology is at hand: Autosomal recessive, defect in enzyme ATP7B—> impaired excretion of Cu2+ into bile, and impaired conversion of Cu2+ to ceruloplasmin —> low levels of ceruloplasmin are Dx criteria for disease. Will cause cirrhosis, basal ganglia degeneration, Parkinson symptoms, hepatic encephalopathy, hemolytic anemia, and increased risk for HCC.
Wilson Disease —> no copper excretion leads to copper deposits in liver, brain (dementia), cornea, kidneys (Fanconi Sd), and joints. In eyes —> Kaiser-Fleischer rings.
Patient presents with impaired ability to protect organs from elastase. Autosomal recessive—> Early-onset panacinar emphysema and cirrhosis. Classically, Px looks waaaaaay too young to have emphysema. What is the deficient substance?
Alpha1-antitrypsin deficiency.
What do K cells produce and from where?
Glucose dependent insulinotropic peptide - duodenum and jejunum
Small intestine produces migrating motor complexes called what?
Motilin
Parasympathetic ganglia in sphincters, gallbladder, and small intestine produce what? It increases water and electrolyte secretion; it increases relaxation of intestinal smooth muscle and sphincters
Vasoactive intestinal polypeptide
Chief cells produce this for protein digestion… production is from where?
Pepsin - stomach