Glycogen breakdown and gluconeogenesis Flashcards

1
Q

how long do dietary carbs last?

A

3-4 hours

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2
Q

how long does glycogen last?

A

30 hours

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3
Q

where is gluconeogenesis done?

A

liver

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4
Q

where does energy between meals come from?

A

adipose triglycerides

muscle proteins if absolutely necessary

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5
Q

where is glycogen broken down?

A

liver and skeletal muscle

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6
Q

what does liver glycogen phophorylase do?

A

cleaves alpha 1,4 linkages by phophoryolysis, releasing 1 G-1-P at a time

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7
Q

what does debranching enzyme do?

A

rearranges the branch so that 1 glucose is left and then cleaves the alpha 1,6 link via hydrolysis, releasing free glucose

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8
Q

how much G-1-P is released? free glucose?

A

G-1-P 92%

free glucose 8%

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9
Q

what is the difference between liver and muscle glycogenolysis?

A

liver has glucose-6-phosphatase which cleaves G-6-P to free glucose which is released into the blood
liver does not

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10
Q

what does glucose-6-phosphatase do?

A

cleaves glucose-6-phosphate to free glucose

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11
Q

what is phosphoglucomutase?

A

isomerizes glucose-1-P to glucose-6-P

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12
Q

what is gluconeogenesis?

A

making glucose

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13
Q

what are the 3 irreversible steps of glycolysis that have to be bypassed during gluconeogenesis? what do they do?

A

hexokinase- changes free glucose to glucose-6-phosphate
phophofructokinase- phophorylates fructose-6-phosphate
pyruvate kinase- changes PEP to pyruvate, releasing ATP

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14
Q

how are the 3 irreversible steps of glycolysis bypassed?

A

pyruvate carboxylase
PEP carboxylase
fructose-1,6-bisphophatase
liver glucose-6-phosphatase

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15
Q

what are the 4 requirements for gluconeogenesis? where do they come from?

A
NADH
energy
Acetyl CoA
Carbons
everything except carbons comes from fatty acid oxidation
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16
Q

what is the energy cost of gluconeogenesis?

A

4 ATP

2 GTP

17
Q

can carbons from acetyl CoA be used in gluconeogenesis?

A

No- pyruvate dehydrogenase is not reversible

18
Q

how can fatty acids be used to make glucose?

A

odd chains are broken down into propinyl-CoA, a 3 carbon compound that can be converted to succinyl-C-A (TCA cycle intermediate, which can form oxaloacetate via TCA cycle

19
Q

what is DHAP? where can it come from? what is it used for?

A

dihydroxyacetone phophate
made from glycerol, fructose
used as a carbon substrate for gluconeogenesis

20
Q

what happens in glycogen storage diseases?

A

glycogen can’t be broken down so it accumulates in cells

due to issues in glycogen breakdown, gluconeogenesis, or fatty acid oxidation

21
Q

what is Von Gierke’s disease?

A

deficiency in liver glucose-6-phosphatase- can’t change G6P to free glucose
symptoms- severe hypoglycemia due to lack of glycogenolysis and gluconeogenesis
cannot be helped by galactose or fructose

22
Q

what are the 3 glycogen storage diseases

A

Von Gierke’s
Hers Disease
McArdles

23
Q

what is Hers Disease?

A

deficiency in liver glycogen phosphorylase
symptoms- milder hypoglycemia (gluconeogenesis works)
can be treated with fructose or galactose

24
Q

what is McArdle’s Disease?

A

deficiency in muscle glycogen phophorylase

symptoms: none, only muscle glycogen can’t be used