Lecture 44: Cholesterol Synthesis and Elimination Flashcards

1
Q

Where is cholesterol mainly found in the cells and what does it do there?

A

Cell membranes and it gives it a certain structure/ rigidity

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2
Q

T/F: The amount of cholesterol from the inside of the cell to the outside decreases.

A

False. It increases as you go from inside to outside of the cell. Organelles with membranes (i.e. nucleus/ ER, etc) have less cholesterol in them than the plasma membrane.

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3
Q

How many carbons are in cholesterol?

A

27 carbons

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4
Q

Which are the most commonly modified carbons in cholesterol?

A

C3 (OH group) and C17 (side chain)

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5
Q

Where is cholesterol synthesized?

A

liver and intestine so it is not required in the diet

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6
Q

What are two common reasons for high cholesterol?

A

Too much cholesterol in the diet

Hyperactively producing cholesterol because of genetic predisposition

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7
Q

How is cholesterol eliminated from the body?

A

Converted into bile acids/ salts in the liver

stored in gall bladder/ secreted into intestine

small percent is excreted in the feces

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8
Q

What is the primary form in which cholesterol is transported in the plasma?

A

Cholesterol ester (esterification at C3 with fatty acid)

Packaged into lipoprotein particles

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9
Q

How do you synthesize HMG CoA?

A

You use thiolase to make acetoacetyl CoA from acetyl CoA.

Then you use HMG CoA synthase on acetoacetyl CoA to make HMG CoA.

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10
Q

What is the rate limiting enzyme for the synthesis of cholesterol?

A

HMG CoA reductase

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11
Q

How much ATP/ NADPH is necessary to make cholesterol?

A

18 ATP
14 NADPH

cholesterol synthesis needs a lot of energy!

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12
Q

Is cholesterol synthesis localized to one portion of the cell?

A

No! It occurs all over the cell (i.e. peroxisomes, ER, cytosol, mitochondria)

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13
Q

What transcription factor regulates cholesterol synthesis genes?

A

SREBP (sterol responsive element binding protein)

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14
Q

How does cholesterol regulated gene expression work when there is high intracellular cholesterol?

A

There is a decrease in transcription of nearly all genes encoding proteins in the cholesterol synthesis pathway

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15
Q

How do you make mature proteolytically processed SREBP?

A

SREBP binds to SCAP (SREBP Cleavage Activating Protein)

When ER sterols are low (low cholesterol) complex moves to golgi where it is cleaved by Protease 1 and 2

Activated SREB moves to nucleus and activates expression of cholesterol synthesis genes

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16
Q

What happens to HMGR when there is an increased level of intracellular cholesterol?

A

HMGR has a decreased stability and it becomes mis-folded and degraded

17
Q

T/F: Phosphorylated HMGR is active.

A

False. HMGR is inactivated by phosphorylation.

It is phosphorylated by AMP kinase.

18
Q

What does insulin and glucagon do to HMGR expression and activity?

A

Insulin stimulates HMGR expression and activity.

Glucagon inhibits HMGR expression and activity

19
Q

What are statins?

A

Statins competively inhibit HMGR. They mimic the transient intermediate mevadyl CoA.

20
Q

Why is there so many different statins?

A

Diversity of medication is important to treat variety of different people.

21
Q

What is the chemical name of Zetia?

A

ezetimibe

22
Q

What does zetia do?

A

It acts as a small intestine brush border.

It has no side effects because it does not enter the blood stream and inhibits the absorption of cholesterol but not triglycerides/ fat- soluble vitamins.

23
Q

What is Vytorin?

A

It is a combination drug of ezetimibe and simavastatin (i.e. a statin) that reduces cholesterol levels when compared to statin alone.

24
Q

Why is Vytorin useful?

A

It permits reduced doses of statins, which have side effects.

25
Q

What is the principal mechanism of eliminating cholesterol from the body?

A

Excretion of bile salts

26
Q

Cholesterol is a precursor to _________.

A

bile salts and bile acids

27
Q

Where are bile salts and acids synthesized, stored and secreted into?

A

Liver
gall bladder
intestine

28
Q

What do bile acids/salts do?

A

they emulsify dietary lipids making them accessible to pancreatic lipases

aid in the absorption of fat soluble vitamins (ADEK)

29
Q

What is the rate limiting enzyme for bile acid formation?

A

7- alpha- hydroxylase

30
Q

What inhibits/ promotes 7 alpha hydroxylase?

A
  • cholic acid

+ cholesterol

31
Q

How do you make a bile acid?

A

You add OH group to the C7 of cholesterol

32
Q

Primary bile acids give rise to _______ which gives rise to ________ which are bile acids conjugated to glycine or taurine in the liver.

A

secondary bile acids

bile salts

33
Q

How do you treat hypercholesterolemia?

A

It is treated with compounds that sequester bile acids in the intestine.

These sequesterants:

  1. prevent the reabsorption of bile acids
  2. increase the conversion of cholesterol to bile acids
  3. increase bile salt elimination in feces