NME 2.29 Flashcards

1
Q

describe the processes involved in lipid metabolism during fed state

A
  • dietary fats are hydrolysed by pancreatic lipase
  • short chain fatty acid enter circulation directly
  • most fatty acid are re-esterified with glycerol in epithelial cells
  • triglyceride enter circulation as chylomicrons
  • fatty acid stored as fat in adipose tissue or reesterified to triglycerides in liver and exported as VLDL
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2
Q

describe the process of lipid metabolism for fasting state?

A
  • fat in adipose tissue hydrolysed to give glycerol and fatty acids during both fasting and exercise
  • fatty acid mobilised and exported to liver and muscles
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3
Q

what does the combination of fatty acid and coenzyme A?

A

acyl-CoA

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4
Q

what is carnitine used for?

A

transport acyl-CoA into mitochondria matrix

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5
Q

what inhibits the transport process during fed state?

A
  • malonyl-CoA
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6
Q

what process does acyl-CoA undergo in the mitochondria?

A
  • beta-oxidation
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7
Q

what are the products of beta oxidation?

A
  • FADH2
  • NADH
  • acetyl-CoA
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8
Q

what is the difference between the beta oxidation in liver and muscle?

A
  • in muscle acetyl CoA oxidise in TCA cycle

- in liver acetyl-CoA converts to ketone bodies

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9
Q

what is the function of hormone sensitive lipase?

A
  • catalyse breakdown of triglyceride to fatty acid
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10
Q

what activates hormone sensitive lipase?

A
  • adrenaline

- glucagon

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11
Q

what inhibits hormone sensitive lipase?

A
  • insulin
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12
Q

describe the function of lipoprotein lipase?

A
  • breaks down chylomicrons and VLDL into chylomicrons remnants which release fatty acid and glycerol
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13
Q

what is lipoprotein lipase activated by?

A

apoCII

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14
Q

what releases lipoprotein lipase?

A

endothelial cells in systemic capillaries

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15
Q

where is ketone bodies synthesized?

A

liver mitochondria

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16
Q

function of ketone bodies?

A

energy source for brain and muscle where they are reconverted to acetyl-CoA then oxidise in TCA cycle

17
Q

what is acetoacetate synthesized from?

A

acetyl CoA

18
Q

what are ketone bodies?

A

water soluble products of fatty acid beta-oxidation

19
Q

when are ketone bodies synthesized?

A

when there is high circulating fatty acids and low insulin concentration

20
Q

what does excessive ketone production cause?

A

metabolic acidosis

21
Q

describe why defects in mitochondrial fatty acid oxidation sometimes manifest as hypoglycaemia?

A
  • defect cause body to be unable to break down adipose stores to provide energy
  • body stores of glucose and glycogen will be depleted
  • inability to produce glucose from mitochondria fatty acid oxidation cause low glucose levels