Section 2 Flashcards

1
Q

Explain what is meant by excitation-contraction coupling

A
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2
Q

Describe the sliding filament theory.

A
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3
Q

Describe what happens during the power stroke.

A
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4
Q

Explain the role of calcium in skeletal muscle contraction.

A
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5
Q

Cross bridges form between _______ and _________

A

Cross bridges form between the myosin HEAD and actin

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6
Q

Describe what occurs during contraction.

A

During contraction, the thin filaments move inwards over the thick filaments.

When this happens, the z-lines move closer together. This occurs simultaneously along the entire fibre and all sarcomeres shorten to the same degree.

Neither the length of the thin filaments or thick filaments themselves changes, just the degree of overlap. As a result, the whole muscle shortens in what is called a
concentric contraction.

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7
Q

What is the power stroke?

A

the interaction between myosin and actin that leads to a shortening of the sarcomere.

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8
Q

What are the steps of the cross-bridge cycle?

A
  1. Binding: Myosin cross-bridge binds to actin molecule
  2. Power stroke: The myosin head bends, pulling thin myofilament inward.
  3. Chevron
  4. Detachment: Cross-bridge detaches at end of power stroke and returns to original
    conformation.
  5. Binding: Cross-bridge binds to more distal actin molecule; cycle repeats.
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9
Q

What is the result of a power stroke in muscle contraction?

A

The result of a power stroke is the actin molecules being pulled closer to the center of myosin molecules.

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10
Q

How does the actin movement change in each successive cross-bridge cycle?

A

On each successive cross-bridge cycle, the actin is pulled even closer to the center of the myosin molecules.

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11
Q

How many actin molecules surround each myosin molecule on each end during a power stroke?

A

Each myosin molecule is surrounded by six actin molecules on each end, all of which are pulled inward simultaneously in muscular contraction.

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12
Q

Are all cross-bridges actively pulling actin at the same time during muscle contraction?

A

No, at any given time, not all cross-bridges are actively pulling actin. Some are holding the actin in position while others prepare for the next power stroke.

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13
Q

How many heads does each myosin molecule have, and how do they act in muscle contraction?

A

Each myosin molecule has two heads, which act independently. Only one of them may be attached to actin at any given time.

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14
Q

What is the energy source for the power stroke in muscle contraction?

A

The energy for the power stroke comes from excitation-contraction coupling, which converts an electrical signal into a muscle contraction.

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15
Q

What is excitation-contraction coupling in muscle contraction?

A

Excitation-contraction coupling is the process of converting an electrical signal (initiated by acetylcholine) into an actual muscle contraction.

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16
Q

What role does acetylcholine (ACh) play in muscle contraction?

A

Acetylcholine is released into the neuromuscular junction, causing permeability changes and initiating an action potential that propagates across the muscle membrane, ultimately leading to muscle contraction.

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17
Q

What are the two membrane structures in skeletal muscle cells that transmit the signal for muscle contraction?

A

The two membrane structures are the Sarcoplasmic Reticulum (SR) and the T-tubules.

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18
Q

What is the function of the Sarcoplasmic Reticulum (SR) in muscle cells?

A

The SR is a membranous structure that serves as a storage site for calcium ions (Ca2+). It is involved in regulating calcium levels for muscle contraction.

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19
Q

What are Transverse tubules (T-tubules), and where are they located in muscle fibers?

A

T-tubules are invaginations of the plasma membrane that run perpendicular to the muscle fibers. They are located at the junction of A and I bands and play a role in transmitting the electrical signal for muscle contraction.

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20
Q

What happens when the plasma membrane depolarizes in muscle cells?

A

The wave of depolarization spreads across the plasma membrane and goes deeper into the cells through the T-tubules, ultimately transmitting the electrical signal for muscle contraction

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21
Q

What is the role of T-tubules in muscle cells?

A

T-tubules are invaginations of the plasma membrane that transmit the electrical signal for muscle contraction from the surface of the muscle fiber to deeper regions of the muscle cell.

22
Q

What are dihydropyridine receptors, and where are they located in muscle cells?

A

Dihydropyridine receptors are voltage-sensors located on the surface of T-tubules. They sense the wave of depolarization as it travels down the T-tubules.

23
Q

What are ryanodine receptors, and where are they located in muscle cells?

A

Ryanodine receptors are located on the sarcoplasmic reticulum (SR), opposite to the dihydropyridine receptors on the T-tubules. They are a type of calcium (Ca2+) channel.

24
Q

How does the wave of excitation influence the ryanodine receptors of the SR?

A

he dihydropyridine receptors on the T-tubules sense the wave of depolarization and influence the ryanodine receptors of the SR to undergo a conformational change, leading to the opening of the ryanodine receptors and the release of calcium (Ca2+) into the cytoplasm.

25
Q

Why is the release of calcium (Ca2+) important in muscle contraction?

A

The release of calcium (Ca2+) is crucial because it is the primary trigger that allows skeletal muscles to contract by enabling cross-bridge formation between myosin and actin.

26
Q

Why can’t muscle contraction occur in a relaxed muscle?

A

In a relaxed muscle, contraction cannot take place because tropomyosin and troponin are positioned to prevent cross-bridge formation by blocking the myosin binding site on the actin molecules. Calcium release is necessary to change the conformation of these regulatory proteins and initiate muscle contraction.

27
Q

What is the cause of muscle relaxation?

A

Muscle relaxation is caused by decreased nerve activity at the neuromuscular junction, leading to the cessation of acetylcholine (Ach) release.

28
Q

How does acetylcholinesterase contribute to muscle relaxation?

A

Acetylcholinesterase is an enzyme that rapidly hydrolyzes acetylcholine (Ach), removing any remaining Ach from the neuromuscular junction. This action stops the generation of action potentials in the skeletal muscle fiber.

29
Q

What happens when action potentials are no longer generated in the skeletal muscle fiber during muscle relaxation?

A

When action potentials cease, the sarcoplasmic reticulum (SR) stops releasing stored calcium (Ca2+), and Ca2+-ATPase pumps on the SR actively pump calcium back into the SR for future use.

30
Q

What is the consequence of calcium removal from the cytosol during muscle relaxation?

A

Without calcium (Ca2+), the troponin-tropomyosin complex can once again cover the actin molecules, preventing cross-bridge formation. This results in muscle lengthening and relaxation.

31
Q

Can you define acetylcholinesterase?

A

Acetylcholinesterase is an enzyme responsible for the rapid hydrolysis (breakdown) of acetylcholine, a neurotransmitter. It plays a crucial role in terminating the action of acetylcholine at the neuromuscular junction and other synapses.

32
Q

Action potential generated in response to binding of acetylcholine and subsequent end-plate potential is propagated across surface membrane and down ___ of muscle cell

A

T-tubules

33
Q

Action potential in T-tubule triggers ___ release from sarcoplasmic reticulum.

A

calcium

34
Q

Calcium ions released from lateral sacs bind to ___ on actin filaments; leads to ___ being physically
moved aside to uncover cross-bridge binding sites on actin.

A

Calcium ions released from lateral sacs bind to troponin on actin filaments; leads to tropomyosin
being physically moved aside to uncover cross-bridge binding sites on actin.

35
Q

________ cross-bridges attach to actin and bend, pulling actin filaments toward the centre of the
sarcomere; powered by energy provided by ________.

A

Myosin cross-bridges attach to actin and bend, pulling actin filaments toward the centre of the sarcomere; powered by energy provided by ATP

36
Q

Calcium is actively taken up by the ___ when there is no longer an action potential

A

sarcoplasmic reticulum

37
Q

With ___no longer bound to ___, ___ slips back to its blocking position over binding sites on
actin; contraction ends; actin slides back into its original resting position

A

With CALCIUM no longer bound to TROPONIN, TROPOMYOSIN slips back to its blocking position over binding sites on actin; contraction ends; actin slides back into its original resting position

38
Q

What allows for ATP-powered cross-bridge cycling during muscle contraction?

A

The exposure of actin binding sites on the actin filaments allows for ATP-powered cross-bridge cycling.

39
Q

What happens when ATP binds to the ATPase site on myosin?

A

When ATP binds to the ATPase site on myosin, it splits into ADP (adenosine diphosphate) and inorganic phosphate (Pi), releasing stored energy that is transferred to the myosin cross-bridge.

40
Q

How is the myosin cross-bridge prepared for the power stroke?

A

The myosin cross-bridge is “cocked” and ready for the power stroke after ATP splits into ADP and Pi, releasing energy.

41
Q

What happens in the presence of calcium ions (Ca2+) during muscle contraction?

A

In the presence of Ca2+, the troponin-tropomyosin complex exposes the actin molecules, allowing the myosin cross-bridge to bind with the actin and initiate the power stroke.

42
Q

What occurs when there is an absence of calcium ions (Ca2+) during muscle contraction?

A

In the absence of calcium ions, the myosin cross-bridge remains “cocked” and contraction will not occur.

43
Q

What happens during the power stroke of muscle contraction?

A

During the power stroke, inorganic phosphate (Pi) is released, and when the power stroke is complete, ADP is also released, but the cross-bridge remains bound to the actin.

44
Q

What causes the cross-bridge to detach from actin during muscle contraction?

A

Binding of a new ATP molecule to the myosin cross-bridge causes it to detach from actin and return to its “un-cocked” state.

45
Q

What is rigor mortis, and why does it occur after death?

A

Rigor mortis is the stiffening of muscles after death. It occurs because the concentration of calcium ions (Ca2+) increases in cells, causing cross-bridges to remain “cocked,” leading to muscle contraction. This continues until ATP is depleted, after which the muscles remain contracted. Rigor mortis eventually resolves when muscle proteins decay.

46
Q

What is the latent period in muscle contraction, and what happens during this period?

A

The latent period in muscle contraction is a brief delay before contraction starts. During this period, cross-bridge cycling begins.

47
Q

How long does a single skeletal muscle action potential typically last?

A

A single skeletal muscle action potential lasts only 1-2 milliseconds (msec).

48
Q

When does peak tension occur in muscle contraction, and what is it?

A

Peak tension, the greatest tension generated while still exerting force against an external load, usually occurs between 40-120 msec after cross-bridge cycling begins. The exact time varies depending on factors like muscle fiber type and location in the body.

49
Q

What is the relaxation time in muscle contraction, and what happens during this period?

A

The relaxation time is the duration of time it takes for all calcium (Ca2+) to be removed from the muscle. It generally takes 50-200 msec from peak tension. During this time, the muscle relaxes.

50
Q

What is a muscle twitch, and what causes it?

A

A muscle twitch is the minimum contraction of a whole muscle caused by a single action potential in the nerve exciting the muscle.

51
Q

Why does the temporal relationship between the action potential and the mechanical response become important in muscle mechanics?

A

Understanding the temporal relationship is crucial for studying muscle mechanics and how muscles contract efficiently. The timing of events during muscle contraction influences the overall function of the muscle.