6 - Lipid Metabolism Flashcards

1
Q

What is the structure of a fatty acid?

A

a molecule containing a hydrocarbon chain with a carboxylic acid group (hydrophilic) at the end

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2
Q

Give an example of a saturated FA

A

stearic acid

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3
Q

Give an example of an unsaturated FA

A

oleic acid

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4
Q

How are fatty acids usually stored within a cel?

A

as triacylglycerols (TAGs)

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5
Q

Triacylglycerols come together to form _____

A

lipid droplets

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6
Q

In mammals, what cells store fatty acids?

A

adipocytes

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7
Q

Where are bile slats produced and stored?

Where are they secreted into?

A

produced in the liver
stored in the gall bladder
secreted into small intestine

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8
Q

What is the role of bile salts?

A

to emulsify fats

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9
Q

What does a lack of bile salts result in?

A

steatorrhoea

because fat passes through the digestive tract undigested and unabsorbed

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10
Q

What easily allows bile salts to interact with TAGs and solute/solvent?

A

hydrophilic and hydrophobic faces

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11
Q

Describe emulsification by bile

A
  • bile salts present the hydrophobic face to TAGs and the hydrophilic face to the solvent
  • this breaks the lipid droplets into small droplets in ‘a soluble form’, increasing the SA
  • pancreatic lipases break the TAGs down
  • results in (TAGs), DAGs, MAGs and FFAs
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12
Q

How are mixed micelles formed from soluble, digested lipid droplets?
What happens to them after they have formed?

A
  • the DAGs, MAGs and FFAs join bile salts, cholesterol, lysophosphatidic acid and fat soluble vitamins to form mixed micelles
  • they are then absorbed by enterocytes in the small intestine
  • TAGs are resynthesised and packaged into chylomicrons
    (chylomicrons = TAGs + other proteins + apoproteins)
  • chylomicrons enter the circulation via lymph
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13
Q

What is orlistat?

A

a potent inhibitor of gastric and pancreatic lipases
designed to treat obesity
reduced fat absorption by 30% (excited by faecal route)

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14
Q

Which body part does not use energy from the β-oxidation/fats?
Where does it get its energy from instead?

A

the brain - uses energy from ketone bodies when glucose supply is low

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15
Q

Where does β-oxidation occur in a cell?

What does it produce?

A

in the mitochondria

results in the formation of acetyl CoA

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16
Q

What is the first step in β-oxidation?

A

fatty acids —–> acyl CoA
enzyme = acyl CoA synthetase
NOTE: ATP —> AMP (2 high energy bonds are used)

17
Q

Where dies the first step in β-oxidation take place?

A

on the outer mitochondrial membrane

18
Q

How do the products of the first step in β-oxidation get into the mitochondria?
What are the enzymes used in this process? What do they do?

A

carnitine shuttle

translocase - to carry carnitine and acylcarnitine across the inner mitochondrial membrane
carnitine acyltransferase I/II - to transfer the acyl group

19
Q

Describe the β-oxidation cycle

What is the overall result of this?

A

OHOT
1- fatty acyl CoA is oxidised (FAD—>FADH2)
2- hydrolysis
3- oxidation (NAD+—>NADH)
4- thiolysis (a molecule of acetyl CoA cleaved off by bringing in CoA and using β-ketothiolase)

the original fatty acyl CoA has been shorted by 2 carbons and a module of acyl CoA has been produced

20
Q

During each cycle of β-oxidation, how many NADH and FADH2 are produced?

A

1 NADH

1 FADH2

21
Q

KEY POINT: Acetyl CoA formed from β-oxidation can only enter the TCA cycle if β-oxidation and carbohydrate metabolism are balanced.
Why is this?

A

because OXALOACETATE is needed for entry of Acetyl CoA into the TCA cycle.

22
Q

If fat breakdown predominates (e.g. when fasting/starving), what does acetyl CoA form instead?

A

KETONE BODIES

  • Acetoacetate
  • D-3-hydroxybutyrate
  • Acetone
23
Q

How many ATP are produced from palmitate β-oxidation?

A

129

24
Q

Where does lipogenesis take place?

A

in the liver, in the cytoplasm of cells

25
Q

What is the order of reactions of elongation (in lipogenesis)?

A

condensation
reduction
dehydration
reduction

26
Q

In lipogenesis, the growing acyl group is linked to an ________

A

Acyl carrier protein

swinging arm mechanism to move fatty acid chain

27
Q

β-oxidation vs lipogenesis:

1) where do each take place?
2) what are the carriers?
3) What are the coenzmes?

A

1) mitochondria vs cytoplasm
2) CoA vs ACP
3) FAD and NAD vs NADPH