Lipids 2 Flashcards

1
Q

Excess acetyl-CoA is exported from teh mitochondria through what pathway?

A

citrate cleavage pathway

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2
Q

What enzyme is used to convert malate to pyruvate?

A

malic enzyme

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3
Q

High citrate concentrations indicates that the CAC is not acble to process all of the acetyl COA from the break dow of carbs meaning what?

A

glycolysis slows down and FA synthesis ramps up

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4
Q

What is the committed/main regulated step of fatty acid synthesis?

A

acetyl coa –> acetyl-CoA carboylase –> malonyl CoA

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5
Q

Enlongation of FAs occurs where?

A

in the ER and mitoc

ER: malonyl coa is the carbo donor
mito: FAs are elongated in a process simliar to reverse B-oxidation

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6
Q

Desaturation of FAs occurs where and requires what?

A

in the ER and requires a p450 MEOS symstem

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7
Q

Synthesis of TAG requires what and comes from where?

A

glycerol; and comes from glycolysis in the well-fed statee

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8
Q

What converts DHAP –> glycerolphosphate?

A

glycerol P dH

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9
Q

glycerol + 3 FAS =?

A

TAG + 3 H2O

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10
Q

In the well-fed state, FA and TAG synthesis increase or decrease? WHY?

A

increase
1. insulin induces expression of acetly-CoA carboxylase, FA synthase, malic enzyme, G6PD

2.

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11
Q

Explain AMP dependent kinase levels.

A

low AMP levels inactivate AMPK, which activates acetyl COA carboxylase and turns on fatty acid synthesis

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12
Q

When is HSL active?

A

in the fasting state.. it gets phosphorylation by PKA which activates HSL; cleavages storage fat and frelease free FAs into circulation

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