Glycogen: Metabolism and Disorders Flashcards

1
Q

What is Glycogen

A

A polymer made from glucose which serves as a form of Energy Store.

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2
Q

The 2 pathways to mantain blood glucose levels during fasting

A

Glycogenolysis and Gluconeogenesis

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3
Q

Which human cell can use only glucose as source of energy

A

Erythrocyte

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4
Q

Where do Glycogenolysis and Gluconeogenesis happen

A

Liver and muscle cells

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5
Q

What is Glycogenesis

A

Conversion of glucose molecules into Glycogen

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6
Q

Regulation of Glycogenesis

A

Allosteric via Glycogen Synthase.
Activated = insulin and cortisol
Inhibited = glucagon and epinephrine.

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7
Q

What is Glycogenolysis

A

Conversion of Glycogen into glucose molecules

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8
Q

Regulation of Glycogenolysis

A

Allosteric via Glycogen Phosphorylase.
Activated = glucagon, epinephrine or AMP
Inhibited = insulin, ATP, glucose-6-phosphate

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9
Q

Insulin is implicated in _________ reactions

A

Anabolic

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10
Q

Glucagon is implicated in ___________ reactions

A

Catabolic

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11
Q

Fed state increases ________ concentration

A

Insulin

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12
Q

Fasting state increases ____________ concentration

A

Glucagon

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13
Q

Insulin promotes which metabolic reactions

A

Glycolysis
Glycogenesis
Fatty acid synthesis
Protein synthesis

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14
Q

Glucagon promotes which metabolic reactions

A

Glycogenolysis
Gluconeogenesis

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15
Q

Glucagon type of signal pathway

A

G-Protein coupled Receptor

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16
Q

First step after Activation of Protein Kinase by glucagon

A

Activation of Glycogen Phosphorylase

17
Q

Insulin type of signal pathway

A

Tyrosine-Kinase receptor

18
Q

Activation of Protein Phospathase-1 by insulin leads to

A

Activation of Glycogen synthase

19
Q

What does the tyrosine-kinase receptor do when stimulated by Insulin

A

Activation of Protein Phosphatase = Activation of Glycogen Synthase

20
Q

Von Gierke disease is cause by deficiency of

A

Glucose-6-phosphatase (LAST STEP in Glycogenolysis)

21
Q

Which molecule is accumulated in Von Gierke Disease

A

Glucose-6-phosphate

22
Q

Von Gierke disease features

A

Clinic: Severe fasting hypoglycemia + Doll-like faces + Hepatomegaly
Lab: Elevated lactate and uric acid

23
Q

Pompe disease is cause by deficiency of

A

Lysosomal alpha 1,4 glucosidase

24
Q

Pompe disease features

A

Cardiomegaly + Exercise intolerance + Weakness

25
Q

Cori disease is caused by deficiency of

A

Debranching enzyme

26
Q

Cori disease special feature

A

Fasitng Hypoglycemia with NORMAL LACTATE levels

27
Q

McArdle disease is caused by deficiency of

A

MUSCLE Glycogen Phosphorylase

28
Q

McArdle disease features

A

Muscle pain w/ exercise + Myoglobinuria + 2ND WIND EFFECT

29
Q

What is the final product of HMP Shunt

A

1 RIBOSE
1 CO2
2 NADPH

30
Q

What reactant does HMP Shunt use

A

Glucose-6phospate

31
Q

Where does HMP Shunt occur

A

Cytosole

32
Q

Regulation of HMP Shunt

A

Allosteric via G-6PD

33
Q

What is G-6PD Deficiency’s inheritance pattern

A

X-Linked Recessive

34
Q

What is G-6PD pathophysiology

A

Deficiency of G-6PD produces a decreases in Reduced Glutathione leading to Oxidative damage

35
Q

G-6PD clinical features

A

Hemolytic anemia in crisis triggered by stressors like Fava Beans, Sulfonamides and infections