Digestion and Energy Pathways

Digestion

  • Digestion starts in the mouth with amylase breaking down carbohydrates (sugar).
  • Lipid and protein digestion do not start in the mouth.
  • Protein digestion starts in the stomach.
    • Stomach acid denatures proteins.
    • Pepsin, derived from pepsinogen from chief cells, breaks peptide bonds.
  • Chewing meat is macro digestion; molecular digestion of proteins begins in the stomach.
  • Triglycerides (fats) are digested by lipase, an enzyme from the pancreas.
  • Bile and pancreatic acid join the GI tract in the duodenum (small intestine).

Duodenum

  • The duodenum neutralizes stomach acid.
  • It contains the ampulla of Vater, where the common bile duct and pancreatic duct merge.

Liver and Gallbladder

  • The liver makes bile.
  • The gallbladder stores bile and contracts to release bile upon sensing fat in food, stimulated by cholecystokinin (CCK).
  • Bile emulsifies fats into micelles.
  • The common bile duct and pancreatic duct enter the duodenum.

Pancreas

  • Has both endocrine and exocrine functions:
    • Endocrine: Produces insulin that goes into the bloodstream.
    • Exocrine: Produces amylase and lipase that go to the stomach.
  • Amylase and lipase, along with bile, enter the duodenum to digest fats and carbohydrates.

Clinical Relevance - Gallstones (Cholelithiasis)

  • Gallstones can move.
  • If a gallstone blocks the common bile duct at the ampulla of Vater:
    • Amylase and lipase back up into the pancreas.
    • This causes acute pancreatitis where the pancreas digests itself due to the backed-up enzymes, leading to a high mortality rate.
  • Risk factors for gallstones and pancreatitis: obesity, fatty foods, smoking, diabetes, and alcohol consumption.
  • Acute pancreatitis pain radiates to the back from the epigastric region.

Energy Conversion

  • The body converts food into energy (ATP) through metabolic pathways.
  • Three primary pathways:
    • Fatty acids (from triglycerides)
    • Monosaccharides (from carbohydrates/starch)
    • Amino acids (from proteins)
  • These pathways converge to produce pyruvate.
  • Each sugar molecule yields two pyruvate molecules, enabling two cycles of the citric acid cycle.

Citric Acid Cycle

  • Also known as the Krebs cycle or Tricarboxylic Acid (TCA) cycle.
  • Pyruvate is converted to acetyl CoA.
  • The conversion of monosaccharides to pyruvate involves eight enzymatic steps (simplified in diagrams).
  • The citric acid cycle also has multiple complex steps (e.g., succinate, isocitrate, fumarate, alpha-ketoglutarate) that are not detailed.
  • Acetyl CoA is oxidized to CO2CO_2 in the citric acid cycle.

Glucose Metabolism

  • Glucose is converted to two pyruvate molecules.
  • Pyruvate enters the TCA cycle (Krebs cycle or Citric acid cycle).
  • The TCA cycle produces reactants (CO2, NADH, and FADH2) that feed into the electron transport chain.
  • The electron transport chain generates most of the ATP (approximately 32 ATP), while the TCA cycle produces a smaller amount (approximately 4 ATP).
  • The body invests ATP to generate more ATP.

Reactants

  • CO2CO_2
  • NADHNADH
  • FADH2FADH_2