Largest gland in the body.
Organized into functional units called lobules.
Contains hepatocytes.
Bile duct collects bile from bile canaliculi between sheets of hepatocytes for secretion from the liver via hepatic ducts.
Functions:
Carbohydrate metabolism: Converts glucose to glycogen (glycogenesis).
Lipid metabolism:
Stores some triglycerides.
Breaks down fatty acids to generate ATP.
Emulsification.
Synthesizes lipoproteins.
Synthesizes cholesterol.
Uses cholesterol to make bile salts.
Protein metabolism: Deaminates amino acids so they can be used for ATP production.
Excretion of bilirubin.
Synthesis of bile salts: Used in the small intestine for emulsification and absorption of lipids.
Stores and concentrates bile.
The liver produces 250–1,500 ml of bile per day.
Bile Composition:
Bile pigments (bilirubin).
Bile salts.
Phospholipids (lecithin).
Cholesterol.
Inorganic ions.
Some molecules released into the bile are reabsorbed in the small intestine.
Bile salts are returned to the liver from the ileum as part of enterohepatic circulation.
About 90%-95% of bile salts are absorbed by the ileum and returned to the liver.
Enterohepatic circulation: Cycle of bile salt secretion by hepatocytes into bile, absorption by the ileum, and resecretion into bile.
Most digestion and absorption of nutrients occur here.
Secretes intestinal juice (water, mucus, and ions).
Receives pancreatic juice enzymes and bile to aid digestion.
Contains brush border enzymes attached to the villi of cells, which are vital for the final stages of digestion.
Mechanical digestion: Involves segmentation in the duodenum.
Chemical digestion: Occurs as chyme mixes with pancreatic juice, intestinal juice, and bile.
Surface area is increased by circular folds, villi, and microvilli to enhance absorption.
Surface area is approximately 200 m^2, about the size of a tennis court.
Simple columnar epithelium with goblet cells and absorptive cells.
Core of lamina propria containing a blood capillary network and lacteal.
Nutrients absorbed by epithelial cells pass through the wall of a blood capillary or lacteal to enter the blood or lymph, respectively.
Microvilli form a fuzzy line called the brush border.
Brush border enzymes are attached to the microvilli of small intestinal absorptive cells.
Some enzymatic digestion occurs at the surface of the absorptive cells lining the villi.
Absorptive cells slough off into the lumen and release enzymes that help digest nutrients in the chyme.
Monomers for carbohydrates and proteins are formed with the help of brush border enzymes.
Capillaries absorb monosaccharides and amino acids, while lacteals absorb chylomicrons (fatty acids and monoglycerides).
Starch digestion begins in the mouth with salivary amylase but stops in the stomach.
50% of dietary starch is digested before it reaches the small intestine.
Continues in the small intestine with pancreatic amylase, breaking complex carbohydrates into oligosaccharides.
Brush border enzymes finish breaking down resulting products and other disaccharides (maltase, sucrase, lactase) in the small intestine.
Monosaccharides are absorbed across the epithelium into capillaries.
Begins in the stomach with pepsin, producing short-chain polypeptides (pH 1.5 - 3.5).
Pancreatic digestive enzymes continue breakdown in the duodenum.
Some brush border enzymes cleave peptide bonds within the interior of a protein; others remove amino acids from the ends of a peptide.
Finishes in the duodenum and jejunum.
Free amino acids are absorbed into capillaries.
Fat digestion begins in the stomach with lingual lipase and gastric lipase.
Fat digestion continues in the duodenum when bile emulsifies the fat into emulsified fat droplets.
Pancreatic lipase acts on the smaller fat droplets to form fatty acids and monoglycerides in the duodenum.
These move into micelles and are transported to the brush border.
Inside the absorptive cells, fatty acids and monoglycerides are regenerated into triglycerides, cholesterol, and phospholipids and combined with proteins to form chylomicrons.
Chylomicrons go through exocytosis into interstitial fluid then diffuse into lacteals.
CHO
Mouth: Salivary amylase digests 50% into oligosaccharides and disaccharides.
Small Intestine:
Pancreatic amylase digests remaining 50% into oligosaccharides and disaccharides.
Brush border enzymes further break these down into monosaccharides, which are then absorbed into the absorptive cells via secondary active transport with Na^+ (for glucose and galactose) or facilitated diffusion (for fructose).
PRO
Stomach: Pepsin breaks down proteins into short-chain peptides.
Small Intestine:
Pancreatic enzymes continue to break down peptides.
Brush border enzymes further digest into amino acids, dipeptides, and tripeptides.
Amino acids are absorbed into the absorptive cells via secondary active transport with Na^+, while dipeptides and tripeptides are absorbed via secondary active transport with H^+.
Triglycerides
Stomach: Activated lingual lipase and gastric lipase break down triglycerides into short-chain fatty acids and monoglycerides.
Small Intestine:
Bile emulsifies fats into smaller fat droplets.
Pancreatic lipase acts on these droplets to form short-chain fatty acids, long-chain fatty acids, and monoglycerides.
Micelles transport these contents to the brush border where they are absorbed into the absorptive cells via simple diffusion.
Inside the absorptive cells, they are reformed into triglycerides, cholesterol, and phospholipids and coated with proteins to form chylomicrons, which enter the lacteals.
Saliva
Salivary Amylase: Digests starches into maltose, maltotriose, and α-dextrins.
Lingual Lipase: Digests triglycerides into fatty acids and diglycerides.
Gastric Juice
Pepsin: Digests proteins into peptides.
Gastric Lipase: Digests triglycerides into fatty acids and monoglycerides.
Pancreatic Juice
Pancreatic Amylase: Digests starches into maltose, maltotriose, and α-dextrins.
Trypsin, Chymotrypsin, Elastase: Digest proteins into peptides.
Carboxypeptidase: Digests peptides into amino acids at the carboxyl-terminal end.
Pancreatic Lipase: Digests triglycerides into fatty acids and monoglycerides.
Ribonuclease: Digests ribonucleic acid into nucleotides.
Deoxyribonuclease: Digests deoxyribonucleic acid into nucleotides.
Brush Border
Enterokinase: Converts trypsinogen to trypsin.
α-Dextrinase: Digests α-dextrins into glucose.
Sucrase: Digests sucrose into glucose and fructose.
Lactase: Digests lactose into glucose and galactose.
Maltase: Digests maltose into glucose.
Aminopeptidase: Digests peptides into amino acids at the amino-terminal end.
Nucleosidases and Phosphatases: Digest nucleotides into nitrogenous bases, pentose sugars, and phosphates.
Terminal part of the GI tract involved in water and ion absorption, where feces are formed and released.
Mechanical digestion involves haustral churning, peristalsis, and mass movement.
Chemical digestion occurs via bacteria.
Chyme from the ileum passes through the ileocecal valve into the cecum.
Concentrates feces by absorbing water, electrolytes, vitamin K, and some B vitamins.
Produces vitamin K and B vitamins via microbial organisms.
Defecation reflex expels feces from the body, assisted by the Valsalva maneuver (voluntary contractions of abdominal muscles).
Enteric nervous system includes the myenteric plexus (controls smooth muscle) and submucosal plexus (controls glands and endocrine cells).
Autonomic nervous system regulation:
Vagus (X) nerve stimulates peristalsis and secretion (parasympathetic).
Contraction of sphincters and inhibition of peristalsis and secretion (sympathetic).