LG 1.8 - Biochem Muscle Metabolism Flashcards

1
Q

When is Anaerobic Metabolism useful?

A

Although anaerobic metabolism is inefficient,
sometime you just feel like moving fast.

Anaerobic metabolism is useful only for extremely short time frames.

anaerobic metabolism can save lives so that later the body can find opportunities to replenish its depleted energy stores.

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2
Q

Aerobic metabolism

ends with the production of _______

A

Pyruvate

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3
Q

Anaerobic metabolism

requires the additional step of reducing pyruvate to lactate. WHY??!

A

Dehydrogenase enzymes interconvert NAD+ and NADH
Need the energy.

NAD+ is an essential substrate of glycolysis.. The NAD+ produced by lactate dehydrogenase exactly balances the NADH produced by glycolysis

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4
Q

What does Anaerobic Metabolism use as fuel?

A

Glucose

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5
Q

What does aerobic metabolism begin with?

A

Acetyl CoA

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6
Q

How many ATP are yielded by Aerobic Metabolism

A

one molecule of glucose yields at most 38 ATP due to variable mechanical loses the net production per glucose molecule is ~30 ATP.

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7
Q

How many ATP and NADH are yielded by Anaerobic Metabolism?

A

yields only 2 ATP and 2 NADH

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8
Q

What does gluconeogenesis use as precursors when created glucose de novo in the liver?

A

liver at some expense in ATP uses precursors that have at least 3 carbons such as: lactate, pyruvate, alanine, and glyerol

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9
Q

The most sensitive signals of low energy within the cell is ___.

A

AMP

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10
Q

Which adenylate will have the greatest change in concentration relative to its initial concentration (ATP, ADP, or AMP?

A

AMP the most sensitive signals of low energy with in a cell.

AMP is normally at such low concentration in the cell
that even a small change in absolute concentration may lead to a 10 fold or 100 fold in relative concentration.

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11
Q

Creatine diet supplement uses

A
  1. increase muscle mass if used after exercise.
  2. have some beneficial effects on muscle mass for elderly if used in combination with other nutrients
  3. damage the liver and kidney if taken in excess.
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12
Q

Creatine Phosphate vs. ATP

A

Creatine phosphate is simpler, more soluble, and less expensive than ATP.
A higher cellular concentration of creatine phosphate is possible, because it can diffuse rapidly through a cell.

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13
Q

Where is creatinine cycled out and how is it created?

A

Creatine spontaneously cyclizes at a slow rate to form creatinine which serves no biological function and is eliminated by the kidneys

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14
Q

What enzyme regulates degradation of glycogen?

A

Glycogen phosphorylase

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15
Q

What is the Creatine Shuttle Hypothesis

A

Creatine not only provides a buffer for high energy phosphate bonds, but it is a transporter that carries high energy phosphoryl groups from the source of ATP production (mitochondria), to the location of ATP hydrolysis (myosin)

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16
Q

Diagram the Creatine Shuttle

A

See slide 12

17
Q

See Slide 2

A

See Slide 2

18
Q

See Slide 3

A

See Slide 2

19
Q

Name the muscle fiber types color, mitocondria, myoglobin, etc

A

See slide 5

20
Q

Explain how, during vigorous exercise, active muscle meets its extreme need for ATP and summarize each of the various relevant mechanisms

A

See Slide 9

21
Q

What enzyme converts Glucose to Glycogen?

A

Glycogen synthase

22
Q

How does glycogen phosphorylase work?

A

Breaks glucose monomers off of glycogen polymers

Uses the energy of glycosidic bond to form a high energy phosphate bond. See slide 12.

23
Q

Is glycogen phosphorylase more regulated by AMP or ATP?

A

AMP.

AMP is a more sensitive indicator of cellular energy than is ADP or ATP

24
Q

Will high AMP concentration stimulate or inhibit glycogen phosphorylase?
Will high ATP concentration stimulate or inhibit glycogen phosphorylase

A

Energy production is generally signaled by low energy compounds.
Energy storage is generally signaled by high energy compoudns.

25
Q

Where is Glycogen Phosphorylase Activity?

A

In the liver. Liver cells export glucose monomers in time of need-gluconeogenesis

26
Q

What are the 3 forms of glucose?

A

G1P, G6P, and F6P

27
Q

What is Von Gierke disease?

What can it lead to?

A

Type I glycogen storage disease. Results from mutations that inactivate glucose-6-phosphatase.

It can lead to hepatomegaly, accumulation of fat and glycogen in the liver

28
Q

What is the function of Myoglobin and Hemoglobin? What are the differences between myoglobin and hemoglobin?

A

Oxygen is transported and stored bound heme groups on proteins, Myoglobin and hemoglobin

Myoglobin globular protein monomer found in muscle

Hemoglobin globular protein tetramer found in blood

See Slide 13 for graph

29
Q

What is excess post-exercise oxygen consumption (EPOC) or oxygen debt?

A

Represents the extra amount of oxygen that must be taken in after strenuous exercise to achieve metabolic homeostasis.

30
Q

Why does hemoglobin bind oxygen less tight than myoglobin inside the muscle tissue?

A
  • Hemeglobin drops oxygen off in the tissues and therefore does not need to bind oxygen as tightly in the tissue.
  • Myoglobin is holding onto that oxygen inside muscle cells and saving it for a time of need, therefore can hold it tighter until necessary to release
31
Q

In muscle, what enzyme converts Pyruvate–>lactate?

A

Lactate dehydrogenase

32
Q

In the liver, what enzyme converts Lactate–>Pyruvate?

A

Lactate dehydrogenase