Carbohydrate Metabolism Flashcards

>70%

1
Q

Where is GLUT1 Located and what is its affinity?

A

Ubiquitous-high in RBCs and Brain. High affinity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

GLUT2 Location and Affinity

A

Liver - Low affinity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

GLUT3 Location and Affinity

A

Neurons - High affinity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

GLUT4 Location and Affinity

Regulated by what?

A

Skeletal Muscle, heart, adipose tissue

-Insulin Dependent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How Does insulin regulate GLUT4

A

signals fusion of GLUT4 vesicles with the plasma membrane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How many molecules of pyruvate from glucose

A

2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the three phases of glycolosis

A

Investment, splitting, payoff

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What does the enzyme hexokinase do?
Where is it located?
What inhibits its action?

A

Glucose to Glucose 6-P
Present in all cells
Inhibited by its product Glucose 6-P

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What does the enzyme glucokinase do?
Where is it located?
What inhibits its action?
What promotes it action?

A

Glucose to Glucose 6-P
Present in (liver and pancreatic b-cells)
Inhibited by glucagon and Fructose 6-P
Promoted by glucose, fructose 1-P, and Insulin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What does the enzyme phosphofructokinase-1 do?
What makes it special for glycolosis?
What inhibits its action?
What promotes its action?

A

Fructose 6-P to Fructose 1,6-BP
It is the rate limiting step in glycolysis
It is inhibited by ATP and Citrate
It is promoted by AMP and Fructose 2,6-BP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q
What does the enzyme glyceraldehyde 3-P dehydrogenase do?
What product(s) are produced?
A

Glyceraldehyde 3-P to 1,3-bisphosphoglycerate

NADH is produced

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
What does the enzyme phosphoglycerate kinase do?
What product(s) are produced?
A

1,3-bisphosphoglycerate to 3-phosphoglycerate

ATP is produced

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q
What does the enzyme pyruvate kinase do?
Is its action reversible or irreversible?
What product(s) are produced?
What inhibits its action?
What promotes its action?
A

phosphonolatepyruvate (PEP) to pyruvate
Irreversible
ATP
It is inhibited by Alanine, ATP, and Glucagon
It is promoted by Insulin and Fructose 1,6-BP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What does F6P do to Glucokinase?

A

It translocates Glucokinase (GK) to the nucleus and acts as an inhibitor.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

When is PFK-1 active

A

Dephosphorylated: kinase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

When is PFK-1 inactive

A

Phosphorylated: phosphatase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

High insulin on Pyruvate Kinase (PK)

A

stimulates protein phosphatase
dephosphorylation of PK
ACTIVE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Low insulin on Pyruvate Kinase (PK)

A

cAMP activates PKA
Phosphorlation
PK INHIBITED

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

For what pathway is Glucose 6-P a precursor

A

Pentose phosphate pathway

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What are the fates of pyruvate?

A

Lactate
Acetyl CoA
Alanine
Ethanol

21
Q

What do disorders of glycolysis cause?

A

hemolytic anemia

22
Q

What mechanism(s) do RBCs use to produce ATP

A

glycolysis

23
Q

Fed State

A
  • abundant glucose
  • increased trapping (phosphorylation)
  • increased rates of glycolosis
  • production of glycogen
  • decreased gluconeogenesis
24
Q

Fasting State

A
  • low glucose
  • decreased uptake
  • more catabolism
  • less storage
  • increase in gluconeogenesis
  • increase in glycogenolysis
25
Type 1 diabetes cause
deficiency due to loss of pancreatic b-cells
26
Type 2 diabetes
insulin resistance hat progresses to loss of b cell function
27
What can defects in some glycolytic enzymes cause
hemolytic anemia | *clinical marker of elevated lactate dehydrogenase
28
What is Tarui Disease (GSD VIII)
Deficient in PFK-1 (rate limiting step of glycolysis) exercise-induced muscle cramps and weakness hemolytic anemia
29
When does gluconeogenesis occur
when glucose and glycogen stores are depleated
30
What are the major precursors of gluconeogenesis
Amino Acids, lactate, and glycerol
31
Where does gluconeogenesis occur
liver kidney small intestine
32
What are positive regulators of gluconeogenesis?
Glucagon, Citrate, cortisol, thryoxine, acetyl CoA
33
What are negative regulators of gluconeogenesis?
ADP, AMP, Fru 2,6-BP
34
What are positive regulators of glycolysis?
Glucose, insulin, AMP, Fructose 2,6-BP, Fru 1,6-BP
35
What are negative regulators of glycolysis
Glucagon, ATP, citrate, Glc 6-P, alanine
36
What are the four important enzymes of gluconeogenesis?
- pyruvate carboxylase - phospohoenolpyruvate carboxylase - fructose 1,6-bisphosphatase - glucose 6-phosphatase
37
What does the enzyme pyruvate carboxylase (PC) do? Where is it located? What is its cofactor?
Pyruvate converted to oxaloacetate (OAA) mitochondrial Biotin is a cofactor
38
What does the enzyme phosphoenolpyruvate carboxykinase (PEPCK) do?
Oxaloacetate (OAA) to phosphoenolpyruvate (PEP)
39
What does the enzyme Fructose 1,6-Bisphosphatase do? Why is this enzyme important for gluconeogenesis? What activates this enzyme? What inhibits this enzyme?
Fructose 1,6-BP to Fructose 6-P Rate limiting step of gluconeogenesis Activated by cortisol and citrate Inhibited by AMP and F2,6-BP
40
What does the enzyme glucose 6-phospohatase do? Where is it active/located What activates this enzyme?
Glucose 6-P to Glucose Only in Liver, kidneys, SI, and pancreas Activated by cortisol
41
What does the Cori Cycle link?
Links the lactate produced from anerobic glycolysis in RBS and exercising muscle to gluconeogenesis in liver
42
What can a deficiency in F1,6-BP cause?
hemolytic anemia, lactic acidosis, hyperventilation
43
What is Fanconi-Bickel Syndrome
Mutation of GLUT 2 transporter - unable to take up glucose, fructose, and galactose - failure to thrive, rickets - treat with vit D
44
What can cause galactosemia
Deficiency in glucose 1P uridyltransferase (GALT) | Deficiency in galactokinase
45
What does the Pentose Phosphate Pathway Produce?
No energy Sugar for DNA and RNA formation Produces NADH
46
What does the PPP do?
Oxidation of G6P to ribulose 5-P | -Reduction of NADP+ to NADPH
47
What does the enzyme G6P dehydrognase do?
Rate limiting step of PPP | reduces NADP+ to NADPH and exidized G6P to 6-phosphoglycono-lactone
48
Where is glycogen stored
liver, muscle, and other tissues