Metabolism VII: TAGs, FAs, and Ketone Bodies Flashcards

1
Q

_______ account for 90-95% of dietary fat.

A

triacylglycerols

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2
Q

Fatty acids account for ______ of biologically available energy.

A

95% (we get a lot of ATP dollars in fatty acid synthesis!)

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3
Q

When there is a need for substrates for energy production, fatty acids are mobilized from what/where?

A

they are mobilized from TAGs in adipose tissue

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4
Q

Hormone-sensitive triacylglycerol lipase (HSTL) is activated by what?

A

cAMP-dependent protein kinase A

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5
Q

What is phosphorylated at the same time as HSTL? What is it necessary for?

A

perilipin, which is necessary for HSTL to translocate to the surface of the fat droplet and hydrolyze TAGs (it is essential for the mobilization of fats in adipose tissue)

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6
Q

Which tissues/organs are good users of fatty acids?

A

liver, renal cortex, heart, skeletal muscle

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7
Q

Which tissues do not / cannot use fatty acids as an energy source?

A

RBCs (lack mitochon.), brain, nervous system, adrenal medulla, lens

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8
Q

Each cycle of beta-oxidation generates…

A

1 acetyl-CoA, 1 NADH, 1 FADH2

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9
Q

How much total ATP is formed from beta oxidation?

A

106

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10
Q

What is the function of carnitine? What does a carnitine deficiency result in?

A

Carnitine transports long-chain fatty acids into the MT matrix for beta-oxidation. Inhibition of transport results in inhibition of FA oxidation and therefore decreased production of ATP.

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11
Q

What is the only known inhibitor of CPT-1?

A

malonyl-CoA

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12
Q

Fatty acids are transported into the mitochondria as _________ for oxidation.

A

acylcarnitines

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13
Q

Broadly describe what beta-oxidation is.

A

It is the catabolic process by which fatty acid molecules are broken down in the mitochondria to generate acetyl-CoA (which enters CAC to generate energy) as well as NADH and FADH2 (which are used in ETC to generate energy)

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14
Q

What is the significance of NADH and FADH2 to the electron transport chain?

A

They are electron carriers that travel down the ETC to release their electrons and facilitate the end result of massive energy production.

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15
Q

Why does malonyl-CoA inhibit CPT-1?

A

It is a product of the rxn catalyzed by Ac-CoA carboxylase (rate-lim. enzyme in FA biosynthesis). FA biosynthesis is counterproductive to FA breakdown, which is why malonyl-CoA (an indicator of FA biosynthesis) inhibits CPT-1 and thus the process of beta-oxidation.

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16
Q

Ketone bodies are synthesized from ______ in _________ when there is a high rate of ____________.

A

acetyl-CoA; liver mitochondria; beta-oxidation of fatty acids

17
Q

What are the 3 main ketone bodies?

A
  • acetone (simplest)
  • acetoacetic acid
  • beta-hydroxybutyric acid
18
Q

True or false: Ketone body biosynthesis occurs only in the liver, but ketone bodies cannot be utilized in the liver.

A

True!

19
Q

Where does ketone body utilization occur?

A

in the mitochondria of muscle, brain, and certain other tissues (heart, renal cortex).

20
Q

What does acetoacetate succinyl-CoA transferase (aka thiophorase) do?

A

It is involved with conversion of ketone bodies to acetyl-CoA, which is used in the TCA to generate energy (this is how tissues derive energy from ketogenesis). It does this by transferring CoA from succinyl-CoA to acetoacetate to ultimately produce acetyl-CoA.

21
Q

What is the rate-limiting enzyme in ketone biosynthesis?

A

HMG-CoA synthase (only found in liver)

22
Q

Where do ketone bodies partition?

A
  • urine

- lungs (specifically acetone, but lungs blow acetone off quickly)