Liver Flashcards
Liver functions
Metabolize carbs, lipids, proteins, bilirubin
Detox
storage of essential compounds
clearing waste products into bile
Liver anatomy
extremely cascular
bi-lobal (connected by falciform ligament)
Right lobe 6x larger
Blood supplied by: hepatic artery (25%) Portal vein (75%)
Liver micro anatomy
Lobules:
Functional units
extretory/metabolic funtions
6 sided
portal triad each corner
Liver cell types
Hepatocytes: 80% of the volume
Kupffer cells: fancy location specific macrocytes
Death in liver failure
24 hours due to hypoglycemia
Liver
Excretion and secretion
Endogenous and exogenous substances in bile or urine
Only organ that gets rid of heme waste
Bile
Bilirubin principle pigment
made of bile salts, pigments, cholesterol, other substances from the blood
Unconjugated bilirubin
Also called indirect
Bound by albumin
insoluble
Conjugated bilirubin
Soluable
Hepatocyte into bile
Urobilinogen
colorless byproduct of bilirubin made by bacteria
Bilirubin processing
RBC -> heme -> unconj bilirubin -> +albumin makes indirect bilirubin -> conjugated bilirubin -> urobilinogen -> excreted in feces, urine, or recirculated
Glycogenesis
storing glucose as glycogen
Glucogenolysis
break down glycogen
Gluconeogenesis
Generate glucose from non carb sources
Lipid metabilism in the liver
Both lipids and lipoproteins
70% daily lipids come from liver and not diet
fatty acids -> Acytal CoA -> triglycerides, phospholipids, Cholesterol
Liver proteins
Almost all synth in liver
Dev Hgb in infants
most important: Albumin
Syth pos/neg acute phase reactants
Liver detox
Gate keeper to the GI tract
First pass effect
Drug detox major function
Pre hepatic Jaundice
Increased bili sent to liver
hemolytic anemias
unconjugated hyperbilirubinemia
Post hepatic Jaundice
Biliary obstruction disease
Gallstones or tumors
conjugated bili can’t be eliminated
bile not brought to intestines - grey poop
Hepatic jaundice
primary problem in liver
bili metabolism and transport defects
Gilbert’s syndrome
autosomal recessive disorder
hepatic jaundice
no clinical consequences
intermittent unconjugated hyperbilirubinemia
Crigler-Najjar
Hepatic jaundice
chronic unconj. hyperbilirubinemia
inherited
type 1: complete abcense of enzymatic conjug
type 2: severe deficiency