Formation and Degredation of Glycogen- Rosenberg Flashcards

1
Q

What tissues are insulin sensitive?

A

Most tissues (skeletal muscles, adipose tissue)

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2
Q

What tissues are insulin insensitive?

A

cornea, lense of the eye, liver, RBCs, WBCs, brain

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3
Q

Explain how GLUT4 and insulin work.

A

Insulin goes to the receptor and sends a signal to a vesicle containing GLUT4 receptors. The vesicle is translocated to the membrane surface by translocation proteins which are activated by protein kinase B (PKB). When insulin levels decrease, the vesicle invaginates back into the cell to be recycled.

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4
Q

Between meals, how does muscle still take in glucose?

A

When muscles contract, the conversion of ATP to ADP occurs. ADP then gets converted to ATP and AMP by adenylate kinase. The rise in AMP levels activates AMP KInase to phosphorylate translocation proteins.

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5
Q

Compare and Contrast Hexokinase and Glucokinase

A

Hexokinase:
Low Km levels, stronger affinity to glucose, non-insulin dependent, usually saturated with substrate, found in both liver and muscle cells, inhibited by its product

Glucokinase:
High Km levels, low affinity to glucose- needs a high concentration of glucose to be active, insulin induced, found only in liver cells, not inhibited

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6
Q

How does glucokinase regulated?

A

It is bound by GKRP in the nucleus of the liver cell until glucose levels rise. Also can be release by a rise in F1P. However, it is inhibited by F6P

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7
Q

Explain the process of creating a strand of glycogen without branching.

A

Glucose gets phosphorylated by glucokinase to G6P.
It then gets converted by G1P by phosphoglucomutase. After, UDP-glucose pyrophosphorylase adds a UDP and it becomes UDP glucose.
Glycogenin starts the chain, and glycogen synthase continues the chain

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8
Q

Explain the process of branching glycogen

A

Branching enzyme cleaves and adds 5-8 units at least 4 units into the chain from the non reducing end

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9
Q

Explain how to take apart glycogen

A

Glycogen phosphorylase works from the non-reducing end and breaks the alpha-1,4 bonds one at a time until reaching 4 units from the branch.
Transferase then comes over and moves 3 units to the larger non-reduced end of glycogen
Alpha-1,6 Glucosidase (Debranching enzyme) hydrolyzed the 1,6 bond to release one unit of glucose

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10
Q

Why can’t muscles cells convert glycogen all the way back to glucose?

A

Muscle cells lack glucose-6-phosphatase which converts G6P back to glucose

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11
Q

When is glycogen phosphorylase active?

A

When it is phosphorylated

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12
Q

When is glycogen synthase active or in the I form?

A

when it is unphosphorylated

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13
Q

What does glucagon do in glycogenolysis?

A

When combined with the receptor, activates a G protein to activate adenylate cyclase which changes ATP to cAMP.
cAMP then activates PKA which has four subunits that phosphorylate glycogen synthase, phosphorylase kinase, and inhibitor-1.
Phosphorylase kinase then phosphorylates glycogen physphorylase
Inhibitor-1 inhibits phosphotase

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14
Q

Can glucagon affect muscle cells?

A

No

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15
Q

Explain activation of Glycogenolysis by Epinephrine

A

Epinephrine can also use the cAMP pathway, but also uses the DAG and Ca pathway

Binds to receptors, activates phospholipase C that changes PIP to DAG and IP3
DAG activates protein kinase C (PKC) that phosphorylates glycogen synthase
IP3 allows the release of Ca. Ca combines with cadmodulin to activate phosphorylase kinase.
Phosphorylase kinase phosphorylates glycogen phosphorylase and glycogen synthase.

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16
Q

What does insulin do for glycogenesis?

A

It activates phosphodiesterase which converts cAMP to AMP
Reverses all the steps that glucagon activates
Activates hepatic phosphatases
Inactivates glycogen synthase kinase

17
Q

Allostericlly, what activates glycogen phosphorylase in the liver?

A

low levels of glucose, G6P, or ATP

18
Q

Allostericlly, what activates glycogen synthase in the liver?

A

high levels of G6P

19
Q

Allostericlly, what activates glycogen phosphorylase in the muscle?

A

low levels of G6P or ATP

high levels of Ca or AMP

20
Q

Allostericlly, what activates glycogen synthase in the muscle?

A

high levels of G6P

21
Q

What is the type, defective enzyme, and the clinical features of the following disease?

Von Gierke’s

A

Type 1
Glucose- 6- phosphatase
Hypoglycemia, Enlarged Liver, Ketosis

22
Q

What is the type, defective enzyme, and the clinical features of the following disease?

Cori’s

A

Type 3
Debranching Enzyme
Milder version of Type 1

23
Q

What is the type, defective enzyme, and the clinical features of the following disease?

Andersen’s

A

Type 4
Branching Enzyme
Cirrhosis of the Liver

24
Q

What is the type, defective enzyme, and the clinical features of the following disease?

McArdle’s

A

Type 5
Phosphorylase
Muscle cramps (usually cant withstand strenuous exercise)
Otherwise normal

25
Q

What is the type, defective enzyme, and the clinical features of the following disease?

Hers’

A

Type 6
Phosphorylase
Milder version of Type 1