L5 glucose metabolism Flashcards

1
Q

what is catabolism/anabolism?

A

catabolism: breaking down complex molecules (exergonic)
anabolism: building of complex molecules (endergonic)

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2
Q

what are the fates of nutrients?

A
  • supply energy
  • serve as building blocks
  • stored
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3
Q

sources of carbohydrate?

A

starch (plant storage)
glycogen (branched glucose)
lactose (glucose and galactose)
sucrose (fructose and glucose)

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4
Q

normal blood glucose levels?

A

90mg/100ml (2-3g)

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5
Q

what is ATP made up of?

A
  • purine base (adenine)
  • five carbon sugar (ribose)
    = adenosine
  • 3 phosphate (attached to sugar by phosphodiester bond)
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6
Q

fate of glucose?

A
  • ATP production
  • Amino acid synthesis
  • Glycogen Synthesis
  • Triglyceride synthesis
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7
Q

GLUT1?

A
  • most tissues
  • low Km/High affinity
  • not affected by insulin
  • works with GLUT3 to allow glucose across blood brain barrier - GLUT1 deficiency therefore impairs flu one transport into the brain (also over expressed in cancers)
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8
Q

GLUT2?

A
  • Hepatocytes
  • regulated by insulin
  • high Km (only transports glucose into cells when blood glucose is high e.g. after eating)
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9
Q

GLUT3?

A
  • has the highest affinity for glucose and high expression in neuronal tissues.
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10
Q

GLUT4?

A
  • striated muscle and adipose tissue
  • in intracellular vesicles in insulin sensitive tissues
  • blood flu raises, insulin released from pancreatic B cells - binds to insulin receptors on plasma membrane - activates insulin signal pathway, GLUT4 translocates from intracellular vesicle to membrane allowing glucose transport.
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11
Q

which GLU transporters are sensitive to insulin?

A

GLUT4

GLUT2

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12
Q

which GLUT are no affected by insulin?

A

GLUT1 and GLUT3

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13
Q

what are the products of glycolysis?

A

net gain of 4 ATP
2 pyruvate
2 NADH+H

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14
Q

fate of pyruvate?

A
  • aerobic = converted to acetyl-coenzyme A and enters TCA cycle
  • anaerobic = reduced to lactic acid by lactate dehydrogenase (or ethanol)
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15
Q

where does galactose enter glycolysis?

A

Galactose is converted to Glu-6-P

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16
Q

where does fructose enter glycolysis?

A

fructose is phosphorylated by hexokinase (in muscle and adipose tissue) to Fruc-6-P

17
Q

describe hexokinase?

A
  • glucose to glucose-6-p
  • inhibited allosterically by its product (G-6-P) - prevents HK using up all the free inorganic phosphate (Pi)
  • low Km/High affinity = all glucose that enters cell is phosphorylated by HK
  • Maintains glucose conc gradient
  • unaffected by insulin
  • will phosphorylate other sugars (fructose - but slower)
18
Q

What happens if Hexokinase is inhibited?

A

Inhibition of HK will suppress Glu uptake into cell bc intracellular conc of glucose will rise

19
Q

describe glucokinase?

A
  • isoenzyme of HK
  • specific for glucose
  • dominant role in liver and kidneys
  • much higher Km (when glucose conc are high GK is only enzyme responding)
  • not inhibited by G-6-P
20
Q

describe phosphofructokinase 1?

A
  • fruc-6-p to fruc,1,6,BP
  • ATP both substrate and allosteric inhibitor
  • inhibited by high levels of ATP
  • AMP and ADP relieve inhibition of PFK1 (therefore the rate of glycolysis depends on the ratio of AMP/ADP)
21
Q

where does gluconeogenesis occur?

A

liver (major store of glucose)

22
Q

what produces insulin?

A

beta cells in pancreas

23
Q

what produces glucagon?

A

alpha cells in pancreas

24
Q

describe pyruvate kinase?

A
  • inhibited by high ATP levels, high ACoA levels, high Glucagon levels
  • regulated by fruc-1,6-BP and insulin
25
Q

function of insulin?

A

lower blood glucose

- stimulates glycolysis and glycogenesis

26
Q

function of glucagon?

A

raise blood glucose

- stimulates gluconeogenesis and glycogenolysis