Part 2 - lecture 1.2 - Quiz Flashcards

(28 cards)

1
Q

Which glucose transporter is bidirectional and why?

A

GLUT2 - liver, pancreas, intestine and kidney - liver and kidney need to be able to deliver glucose out or they would not be able to share it with the environment

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2
Q

What is the most general glucose transporter?

A

GLUT1 - found essentially everywhere

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3
Q

Which glucose transporter is insulin dependent and stimulates muscle and adipose tissue?

A

GLUT4 - muscle and adipose need to tatke up extra glucose when insulin signals because it needs it for storage

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4
Q

Which enzymes are regulated in glycolysis?

A

Hexokinase, PFK1 and pyruvate kinase

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5
Q

In what two ways do hormones regulate activity?

A

By phosphorylation activities or by gene expression level of an enzyme

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6
Q

In what two ways are glycolytic enzymes regulated?

A

Small MW effectors and hormones

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7
Q

Does hexokinase or glucokinase have a higher Km?

A

Glucokinase - specific for glucose is turned on when circulating levels are too high

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8
Q

What happens to glucose in the liver?

A

It can be stored or converted to FAs or modified

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9
Q

What is hexokinase inhibited by? why is this important?

A

It’s product G6P - needs to be turned off so that all of the ATP is not being tied up in the liver cells causing death or damage when continuously signaled

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10
Q

What is glucokinase stored?

A

In the nucleus - bound to a regulatory protein GKRP

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11
Q

What is glucokinase inhibited by?

A

F6P (indirectly) which promotes GKRP binding

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12
Q

What are hexokinase and glucokinase in relation to eachother?

A

isoenzymes

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13
Q

When does glucokinase dissociate from GKRP?

A

WHen glucose levels increase

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14
Q

How is glucokinase hormonal regulated?

A

Inducible by insulin

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15
Q

What does fructose do to glucose utilization?

A

Gets converted to F1P by fructokinase and glucokinase is activated by F1P - causing extra glucose use for FA synthesis

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16
Q

What are the allosteric inhibitors of PFK1?

A

ATP, citrate from TCA, and H+

17
Q

What are the allosteric activators of PFK1?

A

AMP, Fructose-2-6-BP (hormonal)

18
Q

How is PFK1 hormonally regulated?

A

Upregulated by insulin, downregulated by glucagon

19
Q

What does PFK2 do?

A

Produces F-2-6-BP from F6P which activates PFK1 and glycolysis

20
Q

What kind of enzyme is PFK2?

A

Bifunctional - has kinase and phosphatase to produce and eliminate F26BP

21
Q

How is PFK2 controlled by hormones?

A

Glucagon phosphorylates to inactivate the kinase so inactivates glycolysis
Insulin dephosphorylates activate the kinase and activating glycolysis

22
Q

What does epinephrine do to PFK2 in the heart?

A

Phosphorylates activating the kinase and activating glycolysis

23
Q

Explain the pathway of PFK1 in the liver if glucagon is high?

A

High glucagon to low insulin cause increased cAMP which elevates protein kinase A which phosphorylates PFK2 to make it inactivate so fructose 2-6BP isn’t made and PFK1 is not activated so gluconeogenesis instead of glycolysis is favored

24
Q

Explain the pathway of PFK1 in the liver if insulin is high?

A

High insulin to low glucagon decreased cAMP and protein kinase A levels meaning that there is dephosphorylation of PFK2 activating the enzyme to favor the formation of F26BP which activate PFK1 to continue in glycolysis

25
What is pyruvate kinase allosterically regulated by?
Inhibited by ATP and alanine | Activated by F16BP - feed forward
26
How is pyruvate kinase hormonally regulated?
Active in dephosphorylated state which is induced by insulin and inhibited by glucagon
27
Do glucagon and insulin work as kinases or phosphatases?
``` Glucagon = kinase Insulin = phosphatase ```
28
What does a pyruvate deficiency result in?
Hemolytic anemia - rare because RBCs do not get enough glucose that they rely on for energy - pyruvate, lactate and ATP levels remain low causing mature RBCs to lyse -- deficiency results from various defects of the enzyme (may have abnormal Km or Vmax, abnormal response to F16BP, or amount of enzyme decreased or unstable)