Chem path 2s - Lipoproteins Flashcards

1
Q

Outline the structure of atherosclerotic plaques

A

A necrotic core (DEad macrophages) of cholesterol crystals surrounded by foam cells (macrophages) all topped with a fibrous cap

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2
Q

What is the biggest lipoprotein?

A

Chylomicrons

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3
Q

Which lipoproteins are highest in triglycerides?

A

VLDLs and chylomicrons

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4
Q

Which lipoproteins are the main carriers of cholesterol?

A

LDLs

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5
Q

How do we obtain cholesterol?

A

Diet & bile acids or synthesised in the liver

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6
Q

What is the enzyme invovled in the transport of cholesterol across the intestinal epithelium?

A

NPC1L1

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7
Q

Where are bile acids reabsorbed?

A

TErminal ileum

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8
Q

What enzyme does cholesterol downregulate the activity of?

A

HMG-COA-REDUCTASE - this is the main enzyme to produce cholesterol in the liver from acetate and mevalonic acid i.e. the amount of cholesterol synthesised in the liver is dependent on the amount of cholesterol absorbed in the small intestine

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9
Q

what are the two fates of cholesterol which is either made in the liver/brought to the liver?

A

1) Hydroxylation by CYP7A1 enzyme, 7a-hydroxylase –> bile acids
2) Esterified by ACAT –> cholesterol esters and combined with TG and apoB in to VLDL (precursor to LDL)

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10
Q

What is the precursor to LDL?

A

VLDL

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11
Q

Which enzyme is involved in packaging free cholesterol in the peripheries into HDLs?

A

ABCA1

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12
Q

What does CETP mediate the movement of?

A

VLDL –> HDL

HDL –> VLDL

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13
Q

Which genes can be mutated in familial hypercholesterolaemia?

A

LDLR, ApoB, PCSK9 (AD usually)

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14
Q

Which primary hypercholesterolaemia results in longevity?

A

Familial hyper-alpha-lipoproteinaemia = CETP deficiency so increase in HDL

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15
Q

What is the function of pCSK9?

A

Binds to LDLR and promotes its degradation

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16
Q

What are loss of function PCSK9 mutations associated with?

A

Low LDL levels

17
Q

What are the three types of primary hypertriglyceridaemia?

A

Type I, V and IV

18
Q

Type I familial hypertriglyceridaemia?

A

deficiency in apoCII or lipoprotein lipase deficiency –> INCREASED CHYLOMICRONS

19
Q

Type IV familial hypertriglyceridaemia?

A

Increased TG synthesis - INCREASED VLDLs

20
Q

Type V familial hypertriglyceridaemia?

A

apoA V deficiency - INCREASED VLDLs and some CMs

21
Q

Which type of mixed primary hyperlipidaemia is associated with alzheimer’s?

A

Familial dys-beta-lipoproteinaemia - ApoE2 polymorphism. ApoE3 = normal, ApoE4 = increased Alzheimer’s risk, ApoE2 = reduced Alzheimer’s

22
Q

What is a diagnostic sign of famililal dys-beta-lipoproteinaemia?

A

Yellowing of palmar crease

23
Q

Name one example of hypolipidaemia disease

A

Tangier disease

24
Q

What is the mutation of Tangier disease?

A

ABC A1–> HDL deficiency (Features orange tonsils)

25
Q

Outline the pathophysiology of atherosclerosis

A

LDLs become oxidised once it has gone through the vascular wall
Then taken up by macrophages
Within the macrophages the LDLs become esterified and form foam cells

26
Q

Which lipid lowering drug is the best for reducing LDLs and by how much?

A

Statins - ~50% reduction in LDL

27
Q

Which drugs are best at lowering TGs?

A

Fibrates e.g. gemfibrozil

28
Q

How does ezetimibe work?

A

Blocks cholesterol absorption by inhibiting NPC1LI

29
Q

What are the three treatment options for obesity?

A
Low calorie diet + exercise
Iatrogenic malabsorption (orlistat - pancreatic lipase inhibitor)
Bariatric surgery (BMI >40kg/m2)
30
Q

What are the three types of bariatric surgery?

A

Gastric banding
Bypass (Roux-en-Y)
Biliopancreatic bypass

31
Q

What is the definition of success in bariatric surgery?

A

> 50% reduction in excess weight

32
Q

What are the advantages of bariatric surgery?

A
Reduces excess weight
Reduces T2DM risk (72%)
Reduced TGs (50-60%)
Increased HDL
Reduced fatty liver
Reduced HTN
33
Q

Which mode of bariatric surgery reduces Hba1c the most?

A

Biliopancreatic diversion > bypass > medical therapy