Skeletal Muscle Contraction Flashcards

1
Q

What is a sarcomere?

A

functional unit of the muscle fiber

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2
Q

Describe sarcomere structure

A

Three-dimensional cylinder-like arrangement

bordered by structures called Z-discs/Z-lines

Have thick (myosin) and thin filaments (actin)

Has:
A bands
H zone
I bands

Bisecting the H zone is the M line

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3
Q

What are Z-lines?

A

Structures to which actin myofilaments are anchored

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4
Q

What are M-lines?

A

Structures to which myosin filaments are anchored

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5
Q

What do M-lines contain?

A

a myosin-binding protein myomesin (holds the thick filaments in place)

creatine kinase (catalyzes transfer of phosphate groups from phosphocreatine)

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6
Q

What are A bands?

A

The dark bands (where there are myosin myofilaments)

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7
Q

What are I bands?

A

Light bands (portions of the thin filaments that do not overlap the thick filaments)

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8
Q

What is the H zone?

A

Part of the sarcomere which only has myosin and is part of A band

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9
Q

What is excitation-contraction coupling?

A

for a skeletal muscle fiber to contract, its membrane must first be “excited” (stimulated to fire an action potential)

The muscle fiber action potential, which sweeps along the sarcolemma as a wave, is “coupled” to the actual contraction through the release of calcium ions (Ca++) from the SR.

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10
Q

List the steps of the excitation-contraction coupling.

A

1.action potential travels along the axon of a motor neuron.
Individual branches to terminate at the NMJ.

  1. At the NMJ, the axon terminal neurotransmitter, acetylcholine (ACh) is released.
  2. ACh molecules diffuse across the synaptic cleft and bind to ACh receptors within the motor end-plate
  3. A channel in the ACh receptor opens and positively charged ions (Na+) can pass through into the muscle fiber, causing it to depolarize, thus producing a muscle action potential
  4. As the membrane depolarizes, voltage-gated sodium channels are triggered to open.
  5. Sodium ions enter the muscle fiber and an action potential rapidly spreads along t-tubules to initiate excitation-contraction coupling.
  6. triggers the release of calcium ions (Ca++) from its storage in the cell’s SR.
  7. Ca++ then binds to troponin changing its shape and moving tropomyosin on the F-actin to expose the myosin-binding active sites and allow crossbridges to form.
  8. The Ca++ then initiates contraction, which is sustained by ATP
  9. Immediately following depolarization of the membrane, it repolarizes

Meanwhile, the ACh is degraded

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11
Q

What kind of channel does the Ach receptor contain?

A

nonselective cation channel that opens upon neurotransmitter binding

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12
Q

What is the purpose of T-tubules?

A

T-tubules ensure that the membrane can get close to the terminal cisterns of SR in the sarcoplasm.

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13
Q

What is a triad?

A

Arrangement of T tubule with two closely associated small cisterns of sarcoplasmic reticulum on each side

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14
Q

What are the two substances absolutely necessary for muscle contraction

A

ATP and Calcium ions

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15
Q

What is Ach degraded by?

A

acetylcholinesterase in the synaptic cleft

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16
Q

What is the all or nothing law?

A

Individual striated muscle fibers do not show graded contraction—they contract either all the way or not at all.

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17
Q

How do skeletal muscles produce graded contractions?

A

To vary the force of contraction: the fibers within a muscle fascicle do not all contract at the same time.

With large muscles composed of many motor units, the firing of a single motor axon will generate tension proportional to the number of muscle fibres it innervates

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18
Q

What is a motor unit?

A

axon and all the muscle fibers in contact with its branches

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19
Q

What is the cross-bridge cycle?

A

For thin filaments to continue to slide past thick filaments during muscle contraction, myosin heads must pull the actin at the binding sites, detach, re-cock, attach to more binding sites, pull, detach, re-cock, etc.

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20
Q

Describe the steps of cross-bridge cycling?

A
  1. The active site on actin is exposed as calcium binds to troponin. Troponin changes shape and moves tropomyosin out of the way to expose binding site on actin.
  2. Cross-bridge formation
  3. Pi is released, causing myosin to form a stronger attachment to the actin
  4. power stroke
  5. ATP binding causes the myosin head to detach from the actin ATP is converted to ADP and Pi by the intrinsic ATPase activity of myosin.
  6. The energy released during ATP hydrolysis changes the angle of the myosin head into a cocked position. The myosin head is now in position for further movement.
21
Q

What is cross-bridge formation?

A

occurs when the S1 region of myosin attaches to the actin while adenosine diphosphate (ADP) and inorganic phosphate (Pi) are still bound to myosin

22
Q

Describe the power stroke

A

myosin head moves toward the M-line, pulling the actin along with it.

This conformational change is brought about by the rotating of the S1 and S2 regions of myosin.

In the absence of ATP, the myosin head will not detach from actin.

23
Q

What state is the myosin head i when it is cocked?

A

high-energy configuration.

This energy is expended as the myosin head moves through the power stroke

24
Q

Describe the state of myosin at the end of the power stroke

A

at the end of the power stroke, the myosin head is in a low-energy position. After the power stroke, ADP is released; however, the formed cross-bridge is still in place, and actin and myosin are bound together.

25
Q

Why is there rigor mortis after death?

A

With no further ATP production possible, there is no ATP available for myosin heads to detach from the actin-binding sites, so the cross-bridges stay in place, causing the rigidity in the skeletal muscles.

26
Q

List the steps of muscle relaxation

A
  1. The motor neuron stops releasing ACh, into the synapse at the NMJ
  2. The muscle fiber repolarizes
  3. closes the gates in the SR where Ca++ was being released.
  4. ATP-driven pumps will move Ca++ out of the sarcoplasm back into the SR
  5. This results in the “reshielding” of the actin-binding sites on the thin filaments.
  6. Without the ability to form cross-bridges between the thin and thick filaments, the muscle fiber loses its tension and relaxes.
27
Q

What are the functions of ATP?

A

supplies the energy for muscle contraction to take place

ATP also provides the energy for the active-transport Ca++ pumps in the SR

28
Q

How much ATP is stored in muscle?

A

very little

29
Q

What are the mechanisms by which ATP is generated?

A

creatine phosphate metabolism

anaerobic glycolysis

fermentation and aerobic respiration

30
Q

What is creatine phosphate?

A

a molecule that can store energy in its phosphate bonds

31
Q

How is creatine phosphate formed?

A

In a resting muscle, excess ATP transfers its energy to creatine, producing ADP and creatine phosphate.

32
Q

How does creatine phosphate provide more ATP?

A

When the muscle starts to contract and needs energy, creatine phosphate transfers its phosphate back to ADP to form ATP and creatine.

This reaction is catalyzed by the enzyme creatine kinase and occurs very quickly

33
Q

How many seconds worth of energy does creatine phosphate provide?

A

15 seconds

34
Q

What is the difference between glycolysis and creatine phosphate ATP production?

A

Glycolysis cannot generate ATP as quickly as creatine phosphate

35
Q

Where does the sugar for glycolysis come from?

A

blood glucose

metabolizing glycogen that is stored in the muscle.

36
Q

Describe the metabolism in glycolysis

A

The breakdown of one glucose molecule produces two ATP and two molecules of pyruvic acid, which can be used in aerobic respiration or when oxygen levels are low, converted to lactic acid.

37
Q

How is pyruvic acid used if oxygen is available?

A

pyruvic acid is used in aerobic respiration

38
Q

What happens to pyruvic acid when there is no oxygen?

A

pyruvic acid is converted to lactic acid

This may contribute to muscle fatigue.

This conversion allows the recycling of the enzyme NAD+ from NADH, which is needed for glycolysis to continue.

occurs during strenuous exercise when high amounts of energy are needed but oxygen cannot be sufficiently delivered to muscle.

39
Q

How much energy does glycolysis give you?

A

approximately 1 minute of muscle activity

40
Q

How much of the ATP used by resting or mildly active muscle comes from aerobic resp?

A

95%

41
Q

What are the inputs for areobic respiration?

A

glucose circulating in the bloodstream

pyruvic acid

fatty acids.

42
Q

What are the disadvantages of aerobic respiration?

A

cannot be sustained without a steady supply of O2 to the skeletal muscle

is much slower.

43
Q

What are the adaptations which help overcome the problems with aerobic respiration?

A

To compensate, muscles store small amount of excess oxygen in proteins call myoglobin, allowing for more efficient muscle contractions and less fatigue.

Aerobic training also increases the efficiency of the circulatory system so that O2 can be supplied to the muscles for longer periods of time.

44
Q

What are the exact causes of muscle fatigue?

A

unknown

45
Q

What factors have been correlated with muscle fatigue?

A

reduced ATP reserves: This may be more of a factor in brief, intense muscle output rather than sustained, lower intensity efforts.

Lactic acid buildup may lower intracellular pH, affecting enzyme and protein activity.

Imbalances in Na+ and K+ levels as a result of membrane depolarization may disrupt Ca++ flow out of the SR.

Long periods of sustained exercise may damage the SR and the sarcolemma, resulting in impaired Ca++ regulation.

46
Q

What is oxygen debt?

A

the amount of oxygen needed to compensate for ATP produced without oxygen during muscle contraction.

47
Q

What is oxygen used for?

A

restore ATP and creatine phosphate levels

convert lactic acid to pyruvic acid,

In the liver, to convert lactic acid into glucose or glycogen.

Other systems used during exercise also require oxygen

48
Q

How is the S1 region of myosin specialized?

A

It has multiple hinge segments that allows it to bend.