carbohydrate metabolism 3 WF Flashcards

1
Q

glycolytic pathway?

A

glucose-6-P -> fructose-6-P -> fructose-1,6-bisP -> (dihydroxy-acetone-P) -> glyceraldehyde-3-P -> oxidised to produce 2ATP and reduces NAD+ to NADH. produces pyruvate.

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2
Q

glycogen -> pyruvate ATP consumption/production?

A

consumes 1ATP
produces 4ATP
net balance is 3ATP per glucose

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3
Q

glucose -> pyruvate ATP consumption/production?

A

consumes 2ATP
produces 4ATP
net balance is 2ATP per glucose

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4
Q

how is pyruvate reduced to lactate

A

with reoxidation of reduced NADH to NAD+

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5
Q

only source of ATP in red blood cells?

A

anaerobic respiration

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6
Q

name for reverse of glycolytic pathway?

A

gluconeogenesis

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7
Q

where does gluconeogenesis occur

A

liver and kidney

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8
Q

precursors of glucose

A

lactate (from anaerobic metabolism)
glycerol
glucogenic amino acids (protein degradation)

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9
Q

can Acetyl-CoA be converted to glucose?

A

NO!

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10
Q

pentose phosphate pathway occurs in which tissues?

A

liver, adipose tissue, mamillary gland

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11
Q

pentose-phosphate pathway oxidation reactions - products and stuff

A

G-6-P -> ribulose-5-phosphate
with product of CO2 and 2 molecules of NADPH

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12
Q

products of ribulose-5-phosphate and their functions?

A

ribose 5-P used for DNA/RNA synthesis

xylulose 5-P

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13
Q

anti-oxidant function of glutathione?

A

oxygen can react with peptides (especially in RBCs) to produce peroxides (bad)

glutathione reduces peroxides and the glutathione is oxidised to a disulphide which is reduced back to glutathione by reduced NADP

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14
Q

most common genetic disorder in humans? features?

A

G6PDH deficiency
low activity, red blood cells undergo haemolysis. can be exacerbated by drugs.

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15
Q

metabolism of fructose?

A

fructose comes from metabolism of sucrose.
phosphorylated by fructokinase

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16
Q

deficiency of F-1-P aldolase features? (enzyme in fructose metabolism)

A

build-up of fructose-1-P
results in fructose intolerance
consequences are inhibition of glycogen breakdown, gluconeogenesis, oxidative phosphorylation.
-> hypoglycaemia, lactic acidaemia

17
Q

metabolism of galactose?

A

metabolised in liver by galactokinase.
converted to glucose-1-P

18
Q

deficiency of galactose metabolism enzymes causes what?

A

Galactosaemia
galactose-1-P accumulates in liver causing hepatomegaly, jaundice, swelling of eyes, cataracts etc

19
Q

alcohol metabolism features?

A

absorbed in stomach
most important oxidation is alcohol dehydrogenase pathway

20
Q

alcohol dehydrogenase pathway summarised?

A

ethanol oxidised to acetyl-CoA

21
Q

mutation in alcohol oxidation pathway?

A

isoform of aldehyde dehydrogenase in mitochondria with low Km value.

build-up of ethanal, side effects of nausea etc - alcohol intolerance

22
Q

drugs for alcohol addiction? mechanism?

A

disulfiram/Antabuse
inhibits aldehyde dehydrogenase leading to unpleasant symptoms

23
Q

metabolism of toxic alcohols?

A

alcohol dehydrogenase metabolises methanol or ethylene glycol (anti-freeze) to toxic substances

24
Q

inhibition of alcohol dehydrogenase for toxic alcohol ingestion?

A

ethanol (competitive substrate) or fomepizole (inhibitor)