Liver Flashcards
what are the functions of the liver
hormone production, digestion, storage, immune (Kupffer cells) and synthetic functions
what proteins does the liver produce
plasma proteins, clotting factors (except VWF) and compliment proteins
what hormone does the liver metabolise
oestrogen
where is the liver found in the abdomen
in the right upper quadrant (right hypochondriac)
what is the importance of albumin
it maintains oncotic pressure in the vasculature as well as being a carrier protein of unconjugated bilirubin and other hydrophobic molecules
how are faulty proteins degraded
ubiquitin or lysosomal degradation
what is ubiquitin dependent protein degradation
ubiquitin in the cell cytoplasm binds to defective proteins. this signals to proteases that the protein needs to be broken down
what is lysosomal protein degradation
occurs in the reticuloendothelial system in the liver. sinusoidal endothelial cells remove proteins from the blood into a lysosome. Kupffer cells then phagocytose protein in a phagolysosome
what two processes occur in amino acid catabolism
transamination and oxidative deamination
what occurs in transamination of amino acids
where alpha ketoglutarate readily accepts an amine group from alanine. this forms glutamate and pyruvate (to gluconeogenesis or aerobic respiration)
what occurs in oxidative deamination of amino acids
after transamination the glutamate is hydrolysed to form alpha ketoglutarate and ammonia (NH3). the NH3 is then removed via the urea cycle to be excreted
Glutamate plus water - alpha ketoglutarate and ammonia
what enzyme is involved in oxidative deamination
glutamate dehydrogenase
what is negative nitrogen balance
catabolism, where there is more nitrogen out then in
what is positive nitrogen balance
anabolism - more nitrogen in then out
briefly describe the urea cycle starting with citrulline
citrulline joins with NH3 to form arginine. Arginase converts arginine to ornithine, urea is made as a biproduct. ornithine joins with NH3 and CO2 to form citrulline
what is the biproduct of the urea cycle
Urea
what happens if there is a build up of ammonia in the body
it is neurotoxic, it can cross the blood brain barrier and deplete alpha ketoglutarate impairing aerobic respiration
what is the glucose alanine cycle
relationship between muscles and liver so that all muscle energy can go towards contraction and not towards gluconeogenesis
describe the glucose alanine cycle
- reverse transamination in the muscles converts glutamine and pyruvate to alanine and alpha ketoglutarate
- alanine is transported to liver
- in liver transamination occurs and alanine plus alpha ketoglutarate becomes pyruvate and glutamate
- glutamate is oxidatively deaminated
- pyruvate is converted to glucose via gluconeogenesis
- glucose back to muscles
- glucose made into pyruvate and cycle starts again
what is the main source of lipids in the diet
Triglycerides
what is the main functions of lipid in the body
energy reserve (fatty acid beta oxidation), shock absorbent, cell membrane components, hormones and metabolism
what is the energy reserve of blood glucose
40kcal
what is the energy reserve of glycogen
600kcal
what is the energy reserve of muscle protein
30,000kcal
what is the energy reserve of lipids
100,000kcal
what are the different type of lipoproteins
HDLs, LDLs, VLDLs, IDLs
what are HDLs
high density lipoproteins - ‘good’. these are synthesized in the liver and have the highest protein to lipid ratio. they help to remove cholesterol from plasma
what are LDLs
low density lipoproteins - ‘bad’
these are synthesised in the plasma and have low protein to lipid ratio. they deposit cholesterol in the cells
what are VLDLs
they carry triglycerides to adipose tissue
what are IDLs
these are VLDL intermediates and are converted into LDLs
what are the three types of beta oxidation of fatty acids
peroxisomal, mitochondrial and CYP4a ER oxidation
what are xenobiotics
foreign substances that are absorbed but not metabolized
what are the two phases in detoxification
phase 1 oxidation and phase 2 glucuronidation biotransformation
what happens in phase 1 biotransformation of xenobiotics
oxidation - hydrolysis or reduction. this is when an OH group is added onto the molecule which makes the drug more hydrophilic
what catalyzes phase 1 oxidation reaction (detoxification)
CYP450 enzyme (microsomal enzyme)
what happens in phase 2 biotransformation of xenobiotics
glucuronidation - conjugation reaction. you conjugate the drug to a hydrophilic molecule, most commonly glucuronic acid.
what enzyme catalyzes type 2 glucuronidation reaction in detoxification
non microsomal enzymes, most commonly UGT
what happens during alcohol detoxification
alcohol is converted to acetaldehyde (by alcohol dehydrogenase)
acetaldehyde is converted to acetate (by acetaldehyde dehydrogenase)
What does bile contain
bile salts, cholesterol, xenobiotics, electrolytes (HC3-), phospholipids and bilirubin
what is the basic anatomy of the liver
the portal triad is found at the vertices of the hepatic lobules which is hexagonally arranged around the central portal vein