Lipid Metabolism Flashcards

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1
Q

What are the three classes of lipids ?

A

1) fatty acid derivatives - for example phospholipids and triacylglycerols (TAGs).
2) vitamins eg A , D, E and K
3) hydroxy-methyl-glutaric acid derivatives ( c6 compound) for example ketone bodies

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2
Q

In a healthy 70kg man, what is the energy content of triacylglycerols?

A

-600,000kJ

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3
Q

I’m an obese 135 kg man , what is the energy content of triacylglycerols ?

A

-3,000,000kJ

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4
Q

Where are Tag’s stored

A

Adipose tissue

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5
Q

When are TAG’s actually used ?

A

During starvation period , in prolonged exercise , during pregnancy

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6
Q

Storage/mobilisation is under …. control

A

Hormonal

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7
Q

Are tags hydrophobic or hydrophilic

A

Hydrophobic

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8
Q

Outline the process by which dietary fats are metabolised

A

1) bile salts in the small intestine emulsify fats , forming mixed micelles.
2) Pancreatic lipases hydrolyse fats in the small intestine extracellulary.
3) fatty acids and glycerol are recombined into triacylglycerols.
4) they are transported as triacylglycerols by lipoproteins called chylomicrons.
5) released into circulation via the lymphatic system
6) carried to adipose tissue where it is stored as TAGs ( fat mobilisation is hormonally controlled , eg they are metabolised when glucagon and adrenaline are high and insulin is low)
7) carried to consumer tissues as albumin - fatty acid complex

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9
Q

What two cells/tissues do not require triacylglycerols ?

A

1) cells without mitochondria for example red blood cells

2) not the brain as fatty acids do not easily pass through the blood brain barrier

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10
Q

Outline the TAG cycle in the adipose tissue

A

1) when glucose undergoes glycolysis , glycerol-1-phosphate undergoes esterfication with fatty acyl CoA to make triglycerides. This then undergoes lysis which produces fatty acids on albumin and glycerol.

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11
Q

Define amphipathic

A

Contains both hydrophilic and hydrophobic groups

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12
Q

Where does fatty acid catabolism occur

A

In the mitochondria

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13
Q

What is the first step of fatty acid metabolism ?

A

ACTIVATION OF FATTY ACID

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14
Q

Outline the process by which fatty acids are activated and where in a cell does this occur ?

A
  • occurs in the cytoplasm ( not mitochondria).
  • they are activated by combining with coenzyme A.
  • this is aided by the enzyme fatty acyl coA synthase.
  • coA+ fatty acid + ATP = AMP +2pi+ fatty-acyl-coA.
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15
Q

What is the second step of fatty acid metabolism - after they have been activated ?

A

Fatty acyl coA cannot cross the inner mitochondria so they have Carnitine shuttle help.

  • this transports fatty acyl coA across the inner membrane.

-

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16
Q

What is the 3rd step of fatty acid metabolism - after they have been transported across the inner mitochondrial membranes?

A

.Beta oxidation of fatty acids occur.

  • this makes acetyl coA and FADH2 and NADH.
  • acetyl coA can then enter Krebs cycle and FADH2 and NADH can enter oxidative phosphorylation
17
Q

How many carbon units are removed per beta oxidation cycle ?

A

2C

18
Q

Is ATP produced during beta oxidation ?

A

No

19
Q

Does beta oxidation require the presence of O2?

A

Yes;

20
Q

How is glycerol then metabolised ?

A
  • transported to the live .
  • glycerol kinase converts glycerol into glycerol phosphate ( using ATP).
  • this can then be used to make TAGs
  • or it is oxidised to make dihydroxyacetone phosphate (DHAP) which is an intermediate that can enter glycolysis. This in turn makes NADH.
21
Q

What are the three main types of ketone bodies produced in the body ?

A

1) acetone (liver)
2) acetoacetate (liver)
3) B-hydroxybutyrate (liver)

22
Q

What is the normal concentration of ketone bodies in plasma ?

A

Less than 1mM

23
Q

What concentration of ketone bodies would be present in plasma during starvation period

A

2-10 mM

24
Q

At what concentration would plasma ketone bodies rise to in someone who has untreated type 1 diabetes ?

A

More than 10mM

25
Q

How are ketone bodies synthesised ?

A
  • begins with acetylcoA (ch3-coA)
  • synthase converts acetyl coA into hydroxymethylglutaryl (HMG-coA)
  • lyase enzyme then converts HMG-coA into ketone bodies.
26
Q

How is cholesterol produced in the liver ?

A

Begins with acetyl coA

  • synthase converts acetyl-coA into hydroxylmethylglutaryl (HMG-coA)
  • HMG reductase then converts HMG-coA into mevalonate then into cholesterol.
27
Q

When is cholesterol metabolism activated?

A
  • when insulin levels in the blood are high as we are in a fed state.
  • insulin /glucagon ratio is high.
28
Q

When are ketone bodies metabolised - under what conditions ?

A
  • when insulin/glucagon ratio is low.
  • so when glucagon concentration is high.
  • this means we are in a starvation state,

-

29
Q

Ar are ketone bodies water soluble or non soluble ?

A

Water soluble

30
Q

What is ketonuria?

A

Excretion of higher amounts of ketone bodies - associated with diabetes and starvation.

31
Q

Ketosis vs ketoacidosis

A

Ketosis is where during periods of starvation - our body metabolises ketones as fats are used instead of glucose (1-2mM) whereas ketoacidosis is where there is dangerously higher levels of ketones in the plasma ( above 10mM).

32
Q

What is a characteristic smell of someone with ketoacidosis ?

A
  • nail varnish breath due to acetone.
33
Q

ImportantAcne of malonyl- coA

A

Inhibits the carnithine shuttleto ensure that newly synthesised fatty acids are not transported into the inner mitochondria and used for beta-oxidation.

34
Q

In a TAG, what would the reference ‘ 18:3’ represent ?

A

18 carbons

3 double bonds