Cholesterol Flashcards

1
Q

What is cholesterol? How can it be optained

A

A steroid Fatty acid like structure, with 4 ring and a tail-C27, and a hydrophilic head-can force lipid rafts
Can be taken in in diet or storage or made from acCOA

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2
Q

What are key steps in chol biosynthesis? Where does it happen?

A

3 main parts-synthesis of isopentate pyrophosphate (5C) from Ac COA, then 6 IPP to make 30C squalene, (Ctyoplasm)and finally cyclisation and demthylation to make Cholesterol (in ER

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3
Q

What is a key enzyme in chol synthesis?

A

HMG Reductase is rate limiting-target for drugs-statins. Down regulated chol production, and in turn FA absorption and secretion

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4
Q

What is the role of chol in singalling?

A

Cholesterol can make pregnelone by demolase, which is a precusor to all 5 class of hormones (porgesterone, glucocoirticoids, Mineralcorticoids, Androgens and estrogens)

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5
Q

Why do we need vitamin D and sun?

A

Vit D is made from cholesterol, by using ultraviolet light to catalyse a reaction

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6
Q

What is 2 other fate for chol?

A

Can be used to make bile salts-glycocholate and taurocholate. CAn finally also be used to make hedgehog singals

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7
Q

How are Fatty acids transported?

A

As lipoproteins, formed of a hydrophobic core,a nd hydrophilic center-sourounded by proteins that wrap and help recognise. They are usually composed of FA and CE

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8
Q

What are CE and how are they made?

A

CE are cholesterol ester, made from Chol and choline by LCAT-they are very hydrophobic and pack more into the core-making dense lipoprots

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9
Q

What are the different types of lipoproteins and where are they made?

A

Chylomycrons (by enterocytes), VLDL, IDL, LDL, HDL (LIVER)

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10
Q

How are chylomycrons taken up?

A

After entering bloodstream, endothelial tissue wil have LPL on its surface. ACII on Chyl activates LPL, and then parts of the TAG are removed and taken up-remanents continue in the steam until complete uptake

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11
Q

How is LDL uptaken?

A

LDL is made by the liver and sent to other tissues. LDLR-a EGFR like receptor binds LDL and endocytoses in a vesicle-in lysosome, pH difference make the LDL separate, leaving LDLR to be recycled and LDL to be degraded

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12
Q

What is Fh, how many classes of mutation are there and which ones?

A
Familial hyperchoelstermia-recessive
Class i-synthesis
Class II- transport
Class III-binding
Class IV-vesicle formation
Class V-recylcing/release of LDL
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13
Q

What are the treatment options of FH?

A

Statins and Resons/sequestrants

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