Carb Metabolism 4 Flashcards

1
Q

Where does glycogen synthesis occur?

A

liver and muscle

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2
Q

Glucose 6 P —> ? –> gluc 1 p?

A

phosphoglucomutase

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3
Q

glu 1 P –> ? –> UDP glucose?

A

UDP-glucose pyrophosphorylase

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4
Q

Glycogen is synthesized in the cytosol on a primer protein called?

A

glycogenin

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5
Q

What enzymes transfers glucose residues from UDP-glucose to the nonreducing ends of glycogen chains?

A

glycogen synthase

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6
Q

Branching is introduced on glycogen by what enzyme?

A

branching enzyme

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7
Q

When does glycogen degradation occur?

A

when blood glucose levels are low

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8
Q

What enzyme is the first step in glycogen degradation?

A

glycogen phosphorylase

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9
Q

What process involves glycogen phosphorylase, phosphoglucomutase, glucose 6 phosphatase and debranchnig enzymes?

A

glycogen degradation

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10
Q

What process involves hexokinase, phosphoglucomutase , UDP-glucose pyrophosphorylase, glycogen synthase, and branchign enzymes?

A

glycogen synthesis

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11
Q

During glycogen degradation, what is released from debranched chains of a 1,4 linked glucoses?

A

glucose phosphates

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12
Q

Glucokinase is NOT inhibited by what product?

A

gluc 6 phosphate

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13
Q

Glycogen synthase is stimulated by what? Inhibited by what?

A

+ insulin

- glucagon, epinephrine

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14
Q

Insulin ____ blood sugar concentration.
Glucagon _____ blood sugar concentration.
Epinephrine ____ ATP production from glycogen and glucose.

A

lowers
raises
stimulates

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15
Q

Can muscles respond to glucagon? Why or why not?

A

NO!!!! they cannot release glucose as they are lacking glucose 6 phosphatases

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16
Q

In response to epinephrine, what happens in the liver and muscle?

A

stimulates breakdown of glycogen in the liver

activate glycolysis in the muscle to make ATP

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17
Q

Phosphorylation favors glycogen ______?

A

degradation

18
Q

In their phosphorylated states, glycogen phosphorylase is what and glycogen synthase is what?

A

glycogen phosphorylase –> active

glycogen synthase –> inactive

19
Q

Steps of glucagon binding in the liver in response to low levels of glucose.

A
  1. glucagon and epinephrine bind to cell surface receptors.
  2. adenylate cyclase activated
  3. increased cAMP –> activates PKA
  4. PKA activates phosphorylase kinase by phosphorylation
  5. phophorylase kinase phosphorylates glycogen phosphorylase
20
Q

In response to insulin, insulin binds to what type of receptor on the cell to initiate it’s response?

A

protein phosphatase 1 (PP1)

21
Q

What does PP1 do?

A

activates glycogen synthase and inactives glycogen phosphorylase

22
Q

Insulin causes what 4 effects in the liver?

A

activates glycogen synthase
inactiviates glycogen phosphorylase
stimulates glycolysis and ATP generation
no effect on glucose update

23
Q

Glucagon causes what 4 things in the liver?

A

activates, glycogen phosphorylase, glucose 6 phosphatase, and glycogeneogenesis

inhibits glycogen synthase

24
Q

Epinephrine causes what 4 things in the liver?

A

activates glycogen phosphorylase and glucose 6 phosphate

inactivates glycaon synthase

does NOT STIMULATE GLYCOLYSIS

25
Q

Insulin effects in the muscle? 3 thigns

A

stimulates glucose uptake, stimulates glycolysis and ATP, increase muscle glycogen and creatine phosphate levels

26
Q

Effects of glucagon on muscle?

A

NONE

27
Q

Effects of Epinephrine on the muscle?

A

activates glycogen phosphorylase and inactivates glycogen synthase

stimulates glycolysis

28
Q

Before breakfast, what is the main source of blood glucose?

A

gluconeogensis

29
Q

Wha is van Gierke disease?

A

defect in gluocse 6 phosphatase; liver and kidney cannot export glucose and leads to hypoglycemia and increased liver glycogen stores

30
Q

Type 1 glycogen storage disease name?

A

van Gierke

31
Q

Van Gierke is what # glycogen storage disease? WHy?

A

Type 1; defect in glucose 6 phosphatase

32
Q

What is Pompe Disease?

A

deficiency in acid maltase (or a-glucosidease); accumulation of glycogen in the lysosomes over time

33
Q

What is Type II glycogen storage disease?

A

Pompe

34
Q

What is Cori Disease?

A

Type III, disease in glycogen debranching enzyme

35
Q

What is Type 5 glycogen disorder disease?

A

McArdle; defect in muscle glycogen phosphorylase; unable to break down glycogen; muscle cramps during exercise

36
Q

What disease presents with muscle cramps during periods of high glucose demands?

A

McArdle’s; Type 5

37
Q

What are the 2 mechanisms in which alcohol metabolism occurs?

A
  1. Alcohol dehydrogenase and Aldehydge Dehydrogenase

2. p450 system (MEOS)

38
Q

What is one bad thing about the MEOS system?

A

oxidize NADPH; do you wont have as much

39
Q

Ethanol metabolism reduces the amount of what and increases the amount of what in the cytoplasm?

A

decrease NAD and increases NADH

40
Q

What 2 mechanisms are affected when NADH is high?

A

pyruvate and OAA will get converted quickly by Lactate DH and malate DH –> lactate and malate

41
Q

Ethanol metabolism in the liver generates NADH, which reduces the capacity for what and blocks what?

A

reduces the capacity for gluconeogeneis

and blocks CAC