Glycogen Metabolism Flashcards

1
Q

What are the names for glycogen synthesis and breakdown?

A

Synthesis - glycogenesis.

Breakdown - glycogenolysis.

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2
Q

What is the difference in the function of liver and muscle glycogen?

A

Liver: broken down between meals and released to maintain blood glucose levels for RBCs and brain.
Muscle: provides energy via respiration during bursts of physical activity.

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3
Q

What is the primary source of glucose overnight when hepatic glycogen is depleted?

A

Gluconeogenesis.

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4
Q

What are the links joining glycogen and what links introduce branches?

A

α 1-4 glycosidic links, α 1-6 glycosidic links.

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5
Q

What is the protein at the centre of glycogen?

A

Glycogenin.

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6
Q

What is the function of glycogenin and why is this important?

A

It has catalytic properties to add glucose molecules to itself. Glycogen synthase can only add glucose molecules to existing glycogen so glycogen primer of at least 4 glucose required to be attached to glycogenin.

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7
Q

Before glucose can be used in either glycolysis or glycogen synthesis, what needs to happen to it?

A

Needs to be phosphorylated by hexokinase to form glucose-6-phosphate.

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8
Q

What determines whether glucose-6-phosphate will be used for glycolysis or glycogen synthesis?

A

If glucose conc is low, used for glycolysis and vice versa.

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9
Q

What does glucose-6-phosphate need to be converted to before glycogenesis and what enzyme does this?

A

Glucose-1-phosphate. Phosphoglucomutase.

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10
Q

What is a special feature of phosphoglucomutase?

A

It can do forwards and backwards reactions.

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11
Q

What is glucoase-1-phosphate then converted to and what is required?

A

UDP-glucose. Uses a molecule of UTP and UDP-glucose phosphorylase.

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12
Q

What is released when glycogen synthase adds UDP-glucose to the end of the strand?

A

UDP molecule.

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13
Q

What happens to the released UDP molecule?

A

It is phosphorylated to form UTP. For each glucose added to glycogen, 1 ATP is consumed.

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14
Q

What about UDP-glucose makes it highly active?

A

The bond between glucose and the second phosphate group of uridine diphosphate.

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15
Q

What is the bond between UDP and glucose?

A

Phosphate ester linkage.

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16
Q

What is the rate limiting enzyme of glycogenesis?

A

Glycogen synthase.

17
Q

What is the enzyme which introduces branching to glycogen and after how many residues does it do this?

A

Transglycosylase. Every 10.

18
Q

What enzyme is glycogenolysis catalysed by?

A

Glycogen phosphorylase.

19
Q

What does glycogen phosphorylase do?

A

Cleaves a glucose molecule from the glycogen and adds a phosphate to form glucose-1-phosphate.

20
Q

What is the rate limiting step of glycogenolysis?

A

The reaction catalysed by glycogen phosphorylase.

21
Q

What happens to the glucose-1-phosphate once it has been cleaved off glycogen?

A

It is the converted to glucose-6-phosphate by glucophosphomutase.

22
Q

Once glucose has been converted into glucose-6-phosphate, what then happens in the liver?

A

Can be de-phosphorylated by glucose-6-phosphatase and the resulting glucose released into the blood stream via GLUT-2 transporters.

23
Q

Once glucose has been converted into glucose-6-phosphate, what then happens in skeletal muscle?

A

Glucose-6-phosphate cannot be de-phosphorylated, is used to provide energy via glycolysis and the TCA cycle.

24
Q

What does debranching require?

A

Additional enzymes.

25
Q

What enzymes allow regulation in glycogenesis and glycogenolysis?

A

Glycogen synthase (glycogenesis), glycogen phosphorylase (glycogenolysis).

26
Q

What hormone allows regulation of glycogenesis and how?

A

Insulin, indicates high blood sugar so stimulates glycogen synthase and inhibits glycogen phosphorylase.

27
Q

What hormone allows regulation of glycogenolysis and how?

A

Glucagon, indicates low blood sugar so stimulates glycogen phosphorylase and inhibits glycogen synthase.

28
Q

What other hormones can stimulate glycogen phosphorylase?

A

Adrenaline and cortisol.

29
Q

What are glycogen storage diseases and how many types are there?

A

Group of diseases with increase glycogen deposits in liver or muscle or both. 10.