Lipids 2 Flashcards

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
What organs use ketone bodies as fuel during starvation?
brain cells | cardiac and skeletal muscle
26
Where are ketone bodies formed?
in the liver in the mitochondrial matrix
27
How are ketone bodies transported for use elsewhere in the body?
liver can't use ketone bodies | soluble in blood so don't require albumin for transport