Lipolysis, Fatty Acid Oxidation, and Ketogenesis Flashcards

1
Q

describe lipolysis within an adipocyte

A

3 sequential enzymes:

adipose triglyceride lipase (ATGL)
hormone sensitive lipase (HSL)- DG lipase
monoglyceride lipase (MG)-

ATGL and HSL are highly regulated.

HSL uses perlipin

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2
Q

lipoprotein lipase

A

produced within adipocytes, is expressed on the surface and acts on circulating TGs to convert them to FAs for uptake

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3
Q

pancreatic lipase

A

responsible for hydrolysis of ingested TGs in the small intestine

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4
Q

free fatty acids

A

fatty acids circulating in plasma or bound to albumin. available as oxidative fuel

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5
Q

where does fatty acid oxidation take place?

A

in the mitochondria of all cells except brain and RBCs

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6
Q

what protein is responsible for FA uptake into cells?

A

CD36

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7
Q

what happens to FAs after cellular uptake?

A

fatty acyl-CoA synthases catalyze fatty acyl-CoA.

fatty acyl-CoA synthase requirese ATP and pyrophosphatase

however, this cannot pass through the mitochondrial matrix, so it is converted via carnitine acyltransferase 1 (CAT-1) to fatty-acyl carnitine, which is permitted to pass

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8
Q

CAT-1

A

enzyme that converts fatty acyl-CoA into fatty-acyl carnitine for passage into mitochondria. allosterically inhibited via malonyl-CoA, which is in high [ ] when glucose is present

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9
Q

CAT-II

A

reforms fatty acyl-CoA from fatty acyl- carnitine

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10
Q

describe B-oxidation inside the mitochondria

A

oxidation occurs initially at the B carbon, and goes through cycles releasing 2 C acetyl-CoAs. Each cycle produces 1 FADH2 and 1 NADH. The acetyl-CoAs can then enter the TCA, but this requires anapleurotic rxns to form OAA

thus, there must always be SOME glucose oxidation in order for B-oxidation to occur, in order to replenish glucose via pyruvate carboxylase

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11
Q

describe the energy yield per mol of fatty acyl-CoA

A

80 ATP from acetyl CoAs
10.5 from FADH2
17.5 from NADH
ATP utilization -2

106 total per mol

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12
Q

describe ketogenesis

A

occurs only in the liver w/ low levels of oxaloacetate (d/t low levels of glucose), when the acetyl-CoA is shuttled into an alternative pathway

this forms acetoacetate and B-hydroxubuyrate- the ketone bodies

still requires mitochondria, oxygen, OAA, and succinyl-CoA

OAA requirement means need some glucose metabolism

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13
Q

where does ketone oxidation occur?

A

the BRAIN and muscle.

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14
Q

how are ketones taken up?

A

monocarboxylate transporter

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15
Q

how does the energy yield compare to glucose?

A

more energy yielded and less oxygen required

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16
Q

excessive accumulation of ketones causes acidosis

A

ok