Lipids 2 Flashcards

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1
Q

What process does the body utilise to breakdown fatty acids?

A

beta oxidation

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2
Q

Where does beta oxidation occur?

A

mitochondria

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3
Q

What does beta oxidation produce as products?

A

acetyl-CoA which can enter the citric acid cycle
NADH and FADH2 which are used in terminal respiration
ketone bodies

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4
Q

How are free fatty acids transported in the blood?

A

in complex with albumin

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5
Q

How are FAs released from TAG in adipocytes?

A

by hormone sensitive lipase which are triggered by phosphorylation by epinephrine

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6
Q

How does the beta oxidation pathway degrade fatty acids?

A

2 carbons at a time

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7
Q

What are the 3 stages of beta oxidation?

A
  • activation
  • transport
  • degradation
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8
Q

Where does the activation stage occur?

A

the cytosol

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9
Q

What happens in the activation stage?

A

fatty acid activated to form fatty acyl coA in cytoplasm

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10
Q

What happens in the transport stage of beta oxidation? Basics

A

transport of fatty acyl coA from cytosol into matrix of the mitochondrion by mechanism of the carnitine shuttle

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11
Q

How is fatty acyl coA transferred from the cytosol to the matrix by the carnation shuttle?

A
  • fatty acylcoA loses the coA and is transferred by the CAT-1 enzyme into the mitochondrion
  • in the matrix, the fatty acyl recombines with a CoA
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12
Q

What inhibits the carnitine shuttle?

A

malonyl coA

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13
Q

What is the significance of the regulatory action of the presence of malonyl CoA?

A

prevents synthesis and degradation happening at the same time

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14
Q

What is CAT-1 deficiency?

A

no beta oxidation occurs resulting in hypoglycaemia

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15
Q

How is CAT-1 deficiency hypoglycaemia treated?

A

IV glucose

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16
Q

What is the therapy for a CAT-1 deficiency?

A

give medium chain fatty acids that do not require CAT for mitochondrial transport

17
Q

There are 4 stages to the final stage of beta oxidation. What are they? Degradation

A
  1. dehydrogenation to produce FADH2
  2. Hydration
  3. Dehydration to produce NADH
  4. Thiolysis (leaved) to produce acetyl coA
18
Q

What is produced in each beta oxidation cycle?

A

one acetyl CoA and a species two carbons shorter than the original (keeps occurring with 2 carbons chopped off each time)
also FADH2 and NADH

19
Q

How much energy in ATP is produced from beta oxidation of palmitate?

A

129

only 32ATP produced per molecule of glucose!

20
Q

What length of fatty acids undergo preliminary beta oxidation in the peroxisome?

A

> 22 carbons

21
Q

What is a disadvantage of having to have preliminary beta oxidation?

A

first step doesn’t produce FADH2 and so less energy efficient

22
Q

What happens to excess acetyl CoA from beta oxidation?

A

cannot convert acetyl CoA into glucose
in fasting/starvation is converted to ketone bodies or enters the citric acid cycle to be converted to oxaloactetate which can be used in gluconeogenesis

23
Q

What does acetyl CoA inhibit and what does it do?

A

inhibits pyruvate dehydrogenase which is the enzyme responsible for converting pyruvate to Acetyl CoA

24
Q

What does Acetyl CoA activate and what does it do?

A

activates pyruvate carboxylase which converts pyruvate to oxaloacetate which can be used in gluconeogenesis

25
Q

What organs use ketone bodies as fuel during starvation?

A

brain cells

cardiac and skeletal muscle

26
Q

Where are ketone bodies formed?

A

in the liver in the mitochondrial matrix

27
Q

How are ketone bodies transported for use elsewhere in the body?

A

liver can’t use ketone bodies

soluble in blood so don’t require albumin for transport