Acid Secretion in stomach
HCl
Mucosal defenses in the stomach
HCl secretion is risky so body has mechanisms to confine acidity to stomach as much as possible
Parietal (oxyntic) cell
produces HCl and Intrinsic Factor
IF and Vit B12 absorption
Phases of HCl secretion
Interdigestive (basal) phase: between meals following circadian rhythm (highest in evening, lowest in morning b/f waking)
Cephalic phase: mostly neural regulation
gastric phase: initially neural followed by endocrin (gastrin) and neural regulation.
Intestinal phase: mostly endocrine regulation
Parietal Cell receptors
Acid secretion is stimulated by ACh, gastrin, and histamine
Histamine: H2 (increases adenylate cyclase–>cAMP)
ACh: M3 (muscarinic rec)
Gastrin: CCK-B
ACh and gastrin act by increasing intracell Ca.
Ca and cAMP activate protein kinases that phosphorylate H/K ATPase (direct path)
Indirect path: , ACh and gastrin stimulate the ECL (enterochromaffin-like) cells, resulting in secretion of histamine. This histamine then acts on the parietal cell
Peptic ulcer disease (PUD) RFs
H+ and HCO3- transport out of cell and consequence of acid secretion
HCO3- in exchange for Cl- (Cl/HCO3- anion exchanger)
-secondary active transport
(Cl then leaves cell via passive transport and H2O follows– transcellular)
Consequence of acid secretion: pH of venous blood leaving the stomach is high (because of HCO3- transport): alkaline tide.
Phases of gastric acid secretion
Protective barrier of gastric surface
Mucosal barrier and bicarbonate secretion protect mucosa from acid.
The barrier is also prevents diffusional dissipation of the enormous pH gradient
Barrier: surface epithelial cells, mucous (from goblet cells and mucous neck cells), bicarb
Chloride secretion in SI
via cells in crypts
(increased Cl secretion in crypt pushes antimicrobial peptide from paneth cells towards surface where it can act on bacteria)
Digestion
the process of breaking down food into an absorbable form
-some in mouth, stomach, but most in lumen or at surface of absorptive cells (enterocytes)
Absorption
process by which food molecs are transported across the enterocyte membrane (transcellular/cellular) or between cells (paracellular) and into blood or lymph
Largest source of carbs in our diet
plant starch amylopectin
amylase is thus the major enzyme in saliva and pancreatic secretions
Products of amylose/amylopectin digestion: maltose, maltotriose, and alpha-limit dextrin
(sucrose and lactose can be digested at surface of enterocyte)
Which type of sugars can be absorbed?
simple monomeric sugars**
polymers cannot be absorbed
isomaltase
(alpha dextrinase)
converts alpha-limit dextrins to glucose
enterocyte surface
maltase
maltose to maltotriose to glucose
enterocyte surface
lactase
lactose to glucose to galactose
enterocyte surface
sucrase
sucrose to glucose to fructose
enterocyte surface
trehalase
trehalose to glucose
enterocyte surface
Lactose intolerance
SGLT1 transporter
Glucose binds transporter, Conformational change, facilitates binding of Na
Then conf change internalizes transporter
Na dissociates from transporter and moves into cellular space
Na away from transporter–>conformational change
Shift: facing outside again
-glucose and galactose use the same transporter as fructose on the basolateral surface (GLUT2, not Na dependent)
GLUT5 transporter
transports fructose across apical surface,
sodium independent
Regulation of carbohydrate consumption