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ChemPath: Lipoprotein metabolism, CVD and obesity

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

What are the features of an atherosclerotic lesion?

Back (Answer)

• Fibrous cap • Foam cells (macrophages full of cholesteryl ester) • Necrotic core (full of cholesterol crystals)

#2
Front (Question)

What is the biggest plasma lipoprotein?

Back (Answer)

Chylomicrons

#3
Front (Question)

During what time will chylomicrons be most abundant?

Back (Answer)

After eating (they are present in very small amounts in the fasted state)

#4
Front (Question)

Describe the uptake of cholesterol by the intestinal epithelium.

Back (Answer)

• Cholesterol entering the intestines will come from the diet and bile • Cholesterol will be solubilised in mixed micelles • It is then transported cross the intestinal epithelium by NPC1L1 (this is the main determinant of cholesterol transport)

Card back image
#5
Front (Question)

Name two transports that transport cholesterol back into the intestinal lumen.

Back (Answer)

ABC G5 ABC G8

#6
Front (Question)

Where are bile acids absorbed?

Back (Answer)

Terminal ileum

#7
Front (Question)

What happens when cholesterol arrives at the liver?

Back (Answer)

Downregulates the activity of HMG CoA reductase NOTE: HMG CoA reductase is responsible for the production of cholesterol from acetate and mevalonic acid

#8
Front (Question)

What are the two fates of cholesterol that is either produced by or transported to the liver?

Back (Answer)

• Hydroxylation by 7a-hydroxylase to produce bile acids • Esterification by ACAT to produce cholesterol ester which is incorporated into VLDLs along with triglycerids and ApoB

#9
Front (Question)

Which transfer protein is important in the packaging of VLDLs?

Back (Answer)

MTP

#10
Front (Question)

Which transfer protein is important in the packaging of HDLs?

Back (Answer)

ABCA1

Card back image
#11
Front (Question)

What are the effects of CETP on the movement of substances between lipoproteins?

Back (Answer)

• Moves cholesterol from HDL → VLDL • Moves triglycerids from VLDL → HDL

#12
Front (Question)

Which receptor is responsible for the uptake of some HDLs by the liver?

Back (Answer)

SR-B1

Card back image
#13
Front (Question)

Describe the transport and metabolism of triglycerides.

Back (Answer)

• Triglycerides from fatty foods are hydrolysed to fatty acids, absorbed, and resynthesized into triglycerides which are transported by chylomicrons into the plasma • Chylomicrons are hydrolysed by lipoprotein lipase ino free fatty acids • Some free fatty acids are taken up by the liver, and some by adipose tissue • The liver resynthesizes fatty acids into triglycerides and packages them into VLDLs • VLDLs are acted upon by lipoprotein lipase to liberate free fatty acids

Card back image
#14
Front (Question)

List the three causes of familial hypercholesterolaemia (type II).

Back (Answer)

• Caused by autosomal dominant gene mutations in: • LDL receptor • ApoB • PCSK9

#15
Front (Question)

List some mutations that are implicated in polygenic hypercholesterolaemia.

Back (Answer)

• NPC1L1 • HMGCR • CYP7A1

#16
Front (Question)

What is familial hyperalphalipoproteinaemia?

Back (Answer)

• Increase in HDL caused by deficiency of CETP • This is associated with longevity

#17
Front (Question)

What is phytosterolaemia?

Back (Answer)

• Increased plasma concentrations of plant sterols due to mutations in ABC G5 and ABC G8 NOTE: this condition is associated with premature atherosclerosis

#18
Front (Question)

Dsecribe the function of the LDL receptor.

Back (Answer)

• LDLs bind to LDLR in coated pits which then undergo endocytosis (thereby uptaking the LDL into the liver)

Card back image
#19
Front (Question)

List some clinical features of familial hypercholesterolaemia.

Back (Answer)

• Xanthelasma • Corneal arcus • Tendon xanthomata

#20
Front (Question)

What is PCSK9?

Back (Answer)

• A protein that binds to LDL receptors and degrades them NOTE: gain of function mutations result in increased breakdown of LDLR and hence increased plasma LDL levels

#21
Front (Question)

List the key features of the following forms of familial hypertriglyceridaemia: • Familial Type I • Familial Type IV • Familial Type V

Back (Answer)

Familial Type I: • Caused by deficiency of lipoprotein lipase and ApoC II • NOTE: lipoprotein lipase degrades chylomicrons and ApoC II is an activator of lipoprotein lipase Familial Type IV: • Characterised by increased synthesis of triglycerides Familial Type V: • Characterised by deficiency of ApoA V • NOTE: these hypertriglyceridaemias show different patterns when the plasma is left overnight to separate

#22
Front (Question)

What is familial combined hyperlipidaemia?

Back (Answer)

Some people in the family have high cholesterol and others have high triglycerides

#23
Front (Question)

What is familial dysbetalipoproteinaemia (type III)?

Back (Answer)

• Due to aberrant form of ApoE (E2/2) • NOTE: normal form is ApoE (3/3) • A diagnostic clinical feature of yellowing of the palmar crease (palmar striae)

#24
Front (Question)

List some causes of secondary hyperlipidaemia.

Back (Answer)

• Pregnancy • Hypothyroidism • Obesity • Nephrotic syndrome