Lipoprotein metabolism Flashcards
Lipoproteins smallest to largest
Chylomicrons > VLDL > LDL > HDL (2 types - 2 > 3)
Process of cholesterol metabolism
- Dietary cholesterol absorbed across jejenum brush border by NPC1L1 (note ABC G5 + G8 act in opposite direction). More cholesterol is absorbed downstream in the ileum, in the form of bile acids
- Cholesterol goes to liver + down-regulates HMG-coA reductase that synthesises cholesterol de novo
- Either used for bile acid synthesis or esterified by ACAT to form VLDL (LDL pre-cursor)
- LDL can carry cholesterol to the peripheries (bad) or bind LDL receptors on the liver to place cholesterol back in the liver for excretion (better)
- HDL carries cholesterol from peripheries to liver via ABCA1 at periphery + SRB1 at liver
- Cholesterol returned to the liver can be excreted
- CETP transfers cholesterol between LDL + HDL
Process of triglyceride metabolism
- Dietary triglyceride absorbed in small intestine + assembled into chylomicrons
- Chylomicrons hydrolysed by LPL enzyme (in skeletal muscle + adipose tissue capillaries) + free fatty acids released into blood
- Free fatty acids used in liver to form VLDL or incorporated into adipose tissue
VLDL composition
Cholesterol ester
Triglyceride
ApoB
Milky plasma due to excess chylomicrons in blood
LPL deficiency
4 types of dyslipidaemia
Hypercholesterolaemia (high cholesterol)
Hypertriglyceridaemia (high triglycerides)
Mixed hyperlipidaemia (high cholesterol + triglycerides)
Hypolipidaemia (low cholesterol + triglyceride)
Action of PCSK9 inhibitor
PCSK9 inhibitors lower circulating LDL levels
Circulating LDL is a key risk factor for atherosclerosis
PCSK9 binds and degrades LDL receptors on hepatocytes, which normally helpfully remove LDL from the circulation
PCSK9 inhibitors prevent LDL receptor degradation and reduce circulating LDL levels
Main transporters of cholesterol
LDL (70%)
HDL (17%)
Main transporters of triglycerides
VLDL
Chylomicrons
Two main lipids
Triglyceride
Cholesterol
Main carriers of dietary triglyceride absorbed from small intestine
Chylomicrons
LDLR (or less commonly apoB / PCSK9 mutations)
Monogenic AD mutation
Reduced LDL absorption = increased circulating LDL only
(Remains circulating for 5d rather than 2d!)
Heterozygosity > homozygosity
Arcus, xanthelasma, tendon xanthoma, pinpoint ostia
Familial hypercholesterolaemia
3 types - I (LPL deficiency), III and IV (increased TG synthesis)
= Increased circulating TG only
Monogenic AD mutation
Type I = Milky plasma containing chylomicrons if left overnight
Types III / IV = Milky plasma containing VLDL if left overnight
Episodic abdo pain + recurrent pancreatitis
Eruptive xanthoma
Familial hypertriglyceridaemia
Mx familial hypertriglyceridaemia
Depends on cause:
Type I = reduce triglycerides (clearance problem)
Type III/IV = reduce carbohydrates (synthesis problem - reduce carbs to prevent conversion to TG!)
Effect of statins
Reduces LDL
Slight increase in HDL
Moderate reduction in TG