Glycogen synthesis Flashcards

1
Q

Where is excess carbs stored?

A

As glycogen in liver and the muscle

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2
Q

When glycogen reserves are full how is excess carbs stored?

A

As fat

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3
Q

what is the function of glycogen in liver

A

maintenance of blood glucose between meals and during early stages of fasting

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4
Q

what is the function of glycogen in muscle

A

fuel reserve for muscle contraction

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5
Q

Is the glucose released from the liver glycogen exportable?

A

Released into blood to be used by other tissues

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6
Q

Is the glucose released from the muscle glycogen exportable?

A

cannot leave the muscle- enters glycolysis

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7
Q

Hormonal control of liver glycogen

A

Glucagon and adrenaline promotes breakdown.

Insulin promotes synthesis

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8
Q

Hormonal control of muscle glycogen

A

Adrenaline promotes breakdown.

Insulin promotes synthesis.

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9
Q

What happens when the glycogen storage is full

A

converted into fat.

Excess glucose is converted into pyruvate & forms acetyl coenzyme A, excess acetyl CoA forms fatty acids (fat).

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10
Q

Which enzymes are involved in the activation of glucose

A
  1. hexokinase
  2. phospho- glucosmutase
  3. UDP- Gucose pyrophosphorylase
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11
Q

What is the end result when glucose is activated

A

UDP- Glucose

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12
Q

Which Enzymes in the activation of glucose require energy

A
  1. hexokinase ( ATP–> ADP)

2. UDP-Glucose pyrophosphorylase (UTP—> Pi)

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13
Q

What enzyme controls the addition of UDP glucose to glycogen

A

glycogen synthase

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14
Q

What is glycogen synthase controlled by

A

Glucose 6-phosphate

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15
Q

How does Glucose- 6 phosphate control glycogen synthase

A

o If there is plenty of glucose around, there will be a surplus of glucose 6 – phosphate that isn’t being used in glycolysis  so promotes glycogenesis by activating glycogen synthase

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16
Q

Glycogen synthasee is regulated by

A

o Insulin inhibits glycogen breakdown

o Glucagon promotes glycogen breakdown

17
Q

What is the function of the branching enzyme?

A

transfers a block of glucose units from the end of the glycogen polymer to a more interior site

  • o An alpha- 1,4 linkage is broken and an alpha - 1,6 link is formed
18
Q

Deficiency of branching enzyme leads to

A

type IV glycogen storage disease/Anderson’s disease–> causes liver failure and death in first year of life.