Definition: A group of organs that convert food into energy and nutrients.
Key Organs:
Salivary Glands
Liver
Gall Bladder
Pancreas
Major Salivary Glands: 3 pairs
Parotid
Submandibular
Sublingual
Minor Salivary Glands: Numerous microscopic glands throughout the oral mucosa.
Functions:
Lubrication of ingested food and oral mucosa.
Enzymatic digestion of carbohydrates (CHO) and lipids via amylase and lipase.
Metabolism: Substances absorbed by the gut are processed by the liver before entering circulation.
Lipid metabolism: Involves cholesterol, triglycerides (TGs), phospholipids, vitamin A, and fatty acids.
Protein metabolism: Synthesis and degradation of amino acids and proteins; crucial products include albumin and clotting factors.
Carbohydrate metabolism: Formation, storage, and breakdown of glucose and glycogen.
Bile Production: Emulsifies fats and facilitates absorption in the small intestine (SI).
Blood Regulation: Phagocytosis of old or damaged red blood cells (RBCs), pathogens, and debris; metabolism of drugs and toxins.
Outer Layer: Surrounded by a thin fibrous capsule containing fibroblasts and collagenous fibers.
Hepatocytes: The functional cells of hepatic parenchyma, arranged in lobules.
Structure: Hexagonal or pentagonal, surrounded by reticular connective tissue (CT).
Components Include:
Central vein in the middle.
Hepatocytes arranged in plates around the central vein.
Sinusoids interspersed between hepatocyte plates, facilitating nutrient absorption and secretion.
Blood supply from the hepatic portal vein and the hepatic artery flows into the sinusoids.
Components:
Portal venule: Nutrient-rich but low in oxygen.
Hepatic arteriole: Oxygen supply.
Bile ducts: Drainage system for bile.
Hepatocytes: Function as the main cell type with active involvement in metabolism and secrete bile.
Sinusoidal Endothelial Cells: Form the lining of the sinusoids, allowing exchange of substances.
Kupffer Cells: Specialized macrophages that perform phagocytic functions.
Ito Cells: Store vitamin A and can transform during liver injury.
Function: Drain bile produced by hepatocytes; they transport bile from lobule centers to bile ducts.
Structure: Formed by intracellular space between adjacent hepatocytes, leading to canals of Hering and bile ducts.
Components: Right and left hepatic ducts, common hepatic duct, cystic duct (to the gallbladder), and common bile duct (to the duodenum).
Function and Structure: Stores bile (30-50 mL), contains a three-layer wall structure including mucosa, musculosa, and serosa; no muscularis mucosae.
Mucosa Characteristics: Highly folded with simple columnar epithelium; functions in mucus secretion.
Cholelithiasis: Formation of gallstones.
Cholecystitis: Inflammation of the gallbladder.
Choledocholithiasis: Presence of stones in bile ducts.
Cholangitis: Infection/inflammation of bile ducts.
Structure: A mixed exocrine-endocrine gland located retroperitoneally.
Exocrine Functions: Secretion of bicarbonate and digestive enzymes into the duodenum via ducts.
Endocrine Functions: Secretion of insulin and glucagon by the Islets of Langerhans.
Cell Types:
Alpha Cells: Produce glucagon.
Beta Cells: Produce insulin.
Delta Cells: Secrete somatostatin.
Characteristics: Most common pancreatic malignancy (85% of cases); risk factors include smoking and chronic pancreatitis.
Clinical Signs: Jaundice, peripheral venous thrombosis, elevated serum markers (SPan-1, CA19-9).
Cirrhosis: Chronic, irreversible liver disease characterized by widespread necrosis and fibrosis. Causes include chronic viral hepatitis and alcohol abuse.
Appearance: Nodular texture and fibrous tissue formation leading to dysfunctional liver architecture.
Steatosis: Fatty liver condition marked by accumulation of fat within liver cells, can be macrovesicular or microvesicular.
Liver: Processes nutrients, produces bile, regulates blood composition/volume, involved in detoxification.
Gallbladder: Stores and concentrates bile.
Pancreas: Secretes digestive enzymes and hormones that regulate blood sugar.