Gastrointestinal Anatomy and Physiology. Bio 219 Napa Valley College Dr. Adam Ross

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Transcription:

Gastrointestinal Anatomy and Physiology Bio 219 Napa Valley College Dr. Adam Ross

Functions of digestive system Digestion Breakdown of food (chemically) using enzymes, acid, and water Absorption Nutrients, Ions, Water Secretion Mucus, digestive enzymes, acid, bicarb, electrolytes Motility Peristalsis (moves stuff forward) Segmentation (mixes stuff up) ***regional specialization ( assembly line ): ingestion mechanical breakdown chemical digestion absorption waste processing

Structure/ Function of GI Tract GI Tract is a 4 layered tubule Mucosa- epithelium + lamina propria + muscularis mucosae Submucosa- connective and vascular tissue Muscularis externa- smooth muscle- inner circular, outer longitudinal Serosa- thin covering membrane

Mouth, Pharynx, Esophagus Functions: ingestion, mastication (chewing), deglutition (swallowing) Salivary glands: secrete saliva which contains amylase and lipase Amylase begins digestion of starches into disaccharides Lipase begins to digest lipids Esophagus: swallowing (upper), peristalsis (lower) Lower esponageal sphincter control entry to stomach

Stomach Functions: storage, mechanical breakdown of food (chime), chemical digestion (HCl and pepsin) Structure: mucosa: simple columnar epithelium, gastric glands - secrete acidic gastric juice (ph 1-2), 1-3 L/day - mucous cells secrete alkaline mucus to protect stomach epithelium muscularis: 3 layers thick - pyloric sphincter controls passage of chyme from stomach to duodenum

Acid secretion in stomach parietal cells secrete hydrochloric acid (HCl) CO2 + H2O H2CO3 H+ + HCO3- H+ is active transported into the lumen, Cl- follows via diffusion through channels HCO3- is transported back into ECF (countertransport with Cl-)

Enzyme secretion in stomach chief cells secrete pepsinogen (inactive), activated at low ph to form pepsin pepsin digests proteins into smaller peptides

Small Intestine, Liver, and Pancreas functions: chemical digestion and absorption SI regions: duodenum, jejunum, ileum a. Digestion - duodenum receives chyme from stomach, secretions from liver and pancreas Liver - processes absorbed nutrients (delivered via hepatic portal vein) - secretes bile, stored in gallbladder bile salts - derived from cholesterol, function to emulsify fats micelles bile pigments (bilirubin, biliverdin) - waste products from hemoglobin breakdown Pancreas - acinar cells secrete digestive enzymes: trypsin, chymotrypsin, carboxypeptidase, amylase, lipase many enzymes are secreted in inactive form (zymogens), activated by trypsin in lumen - duct cells secrete bicarbonate (NaHCO3) to neutralize acid (ph 8) SI (brush border) enzymes complete digestion

Absorption in SI Absorption - small intestine has huge surface area, specialized for absorption (1) length > 3 meters (2) circular folds (3) villi - epithelium (enterocytes and goblet cells) + lamina propria (capillaries and lacteals) (4) microvilli - brush border membrane - Na+, Cl-, K+ absorbed via active transport and diffusion through channels - glucose & amino acids - cotransport with Na+ (secondary active transport) - H2O - via osmosis, follows solute transport water-soluble nutrients are absorbed into intestinal capillaries liver (via HPV) lipids are formed into chylomicrons and absorbed into lymphatic vessels (lacteals)

Large Intestine functions: fluid absorption, waste packaging and elimination - LI absorbs most remaining water and ions from chyme - intestinal microflora - bacteria in colon, produce some vitamins (K, B12) - defecation reflex

Neural Control 1. Enteric Nervous System - submucosal and myenteric plexuses - local control within the GI tract (short reflex) 2. Autonomic Nervous System parasympathetic: vagus nerve - stimulates GI tract motility and secretion (long reflex) sympathetic division mostly inhibits GI tract

Enteric Nervous System (ENS) Primary neural mechanism that controls GI function Neurons mostly found in: Submucosal (Meisner s) plexus and Myenteric (Auerbach s) plexus

SM Action Potentials SM can have different types of action potentials: spike, spike followed by a plateau, spikes on slow waves

In the small intestine the interstitial cells of Cajal have pacemaker activity and create slow wave Aps (BER)- normal is 12 cycles per minute Neural stimulation can modify contraction rate and strength but is not necessary to initiate contraction Voltage-gated Ca channels that are active at resting membrane potentials open -> influx of Ca depolarizes the cell and opens more voltage gated Ca channels -> increase in Ca activates Cadependent K channels that open and repolarize the cell; voltage gated Ca channels also inactivate

Parasympathetic Innervation Parasympathetic neurons travel along the vagus nerve and synapse with the ENS or directly to the GI tract Release ACh as the neurtransmitter on effector cells ACh release will result in an increase in baseline tension, but does not change the frequency of contraction

Sympathetic Innervation Sympathetic neurons travel through the splanchnic nerve and can synapse to the ENS or directly to effector cells Release Norepinephrine as neurotransmitter on effector cells Results in a decrease in tension, but does not change contraction frequency

Hormonal Control gastrin - secreted by G cells in the gastric glands - stimulates gastric acid secretion; stimulates gastric motility and mucosal growth (- acid secretion is also stimulated by histamine secreted by ECL cells in gastric glands) CCK (cholecystokinin) - secreted by endocrine cells in intestinal crypts - stimulates bile release from gallbladder and pancreatic enzyme secretion secretin - stimulates bicarbonate secretion by pancreas GIP (gastric inhibitory peptide) - stimulates insulin secretion by pancreas; - GIP, CCK and secretin all inhibit gastric acid secretion