Skeletal muscle AP II Flashcards

1
Q

Are muscle fibres self activated?

A

No they are under voluntary control of the CNS

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2
Q

Where are the nerve cells that activate the skeletal muscle fibres?

A

In the spinal cord, they are called motor neurons. They form a very long axon that extends into the periphery and makes synaptic contact with muscle fibres at a single pt called the NMJ

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3
Q

What are motor neurons activated by?

A

Activated by cells in the brain called the motor cortex.

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4
Q

What is spcialised synapse NMJ?

A

It is the myelinated axon termination point of a motor neuron where the brain sends an AP (membrane potential change) to the muscle fibre sarcolemma (excitable cell) to initiate contraction in the muscle fibre

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5
Q

What kind of synapse is NMJ

A

It’s an excitatory synapse (no skeletal muscles are inhibitory)

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6
Q

What is a motor unit?

A

A motor neuron and all of the muscle fibres it controls

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7
Q

Does one motor neuron branch to many different muscle fibres?

A

Yes

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8
Q

Where are motor neurons found?

A

Ventral part of the spinal cord

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9
Q

How are spinal nerves formed?

A

The motor axons branch out from the spinal cord to form vental nerve roots –> spinal nerves

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10
Q

How are muscle fibres innervated?

A

Axons project together and then branch out in the muscle and connect to the muscle fibres

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11
Q

Is a whole muscle a collection of motor units?

A

Yes, motor neurons whose axons project to the same muscle lie close together on the spinal cord

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12
Q

Function of very big motor units

A

Provide a lot of force but can’t provide fine increment control

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13
Q

What is recruitment?

A

Amount of motor neurons activated at any one time that can be varied to change the amount of force produced

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14
Q

Where is the NMJ located?

A

Usually at the middle 3rd of the fibres length so that the AP can spread over the sarcolemma away from NMJ in both directions

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15
Q

What is myosin?

A

The myofilament inbetween actin, it has a long tail and a globular head that can flex i.e its site of binding and “walking” along Actin

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16
Q

What is Actin?

A

It is a globular protein (G-actin) that assemble to form a filamentous protein strand of (F-Actin)

In the sarcomere, the strands that conect to the ends of the z line are two of the filamentous protein strands

17
Q

What is tropomyosin?

A

It is a thin strand that runs along each of the two Actin strands, it blocks the sites where myosin interacts with actin (at rest)

18
Q

What is troponin?

A

Globular protein found throughout tropomyosin and actin, controls the rolling of tropomyosin that makes the binding sites of actin available

19
Q

What is excitation-contraction coupling?

A

aka EC - coupling
*Plasma membrane excitation –> Ca2+ release –> muscle contraction

20
Q

What is the protein that detects a change in the Voltage of the transverse tubule?

A

DHPR - Dihydropyridine

21
Q

How does EC occur?

A

*AP from nerves causes snaptic transmission at NMJ to trigger AP in muscle fibre
*Muscle AP spreads over surface of sarcolemma and invades the T - tubular system
*Detection of membrane potential change causes the Ryanodine receptor (RyR), which releases Ca2+ from reserves into the Cytoplasm of the cell
*Ca2+ binds to the troponin C on the actin filaments, changes the shape of troponin and causes the tropomyosin to roll due to change in shape.
*Exposure of actin to myosin, filaments slide against each other to contract and produce force
*For relaxation, Ca2+ unbinds, goes back to cytoplasm from the contractile apparatus, and goes through SERCA (uses ATP to pump Ca back)

22
Q

What is SERCA

A

Sarco(endo) plasmic reticulum Ca2+ ATP ase

23
Q

What is cross bridge cycling?

A

Process of contraction in the myofilaments

24
Q

What happens in the cross bridge cycling process?

A

*When Ca2+ levels are low, ADP is found to the myosin and is kept in a cocked state, ready to bind to Actin
*Ca2+ released from the EC coupling
*Ca2+ binds to troponin, rolling away the tropomyosin and exposing the myosin binding sites on F-Actin
*Myosin head makes contact with Actin and rotates its head while Actin contracts –>
* ADP released causeing flexion (change in shape of the myosin head) –> “power stroke” of the myosin head. The contact between A and M is called “Cross bridge”
*If ATP available, it binds to free myosin head, causes lowering of affinity of myosin to actin, breaks the cross bridge.
*ATP hydrolised by myosin ATP ase –> ADP + Pi, the energy released is used to bring back the myosin head to the “cocked phase”

25
Q

Muscle tension depends on two things:

A

*Rate of stimulation i.e the amount of APs
* No. of muscle fibres recruited for the task

26
Q

Frequency of stimulation - Twitch

A

*One AP generates a single twitch. If MF restimulated after complete relaxation, second twitch is the same magnitude as the first

27
Q

Frequency of stimulation - Twitch summation

A

If muscle fibre has not relaxed before restimulation, sum of twitches = twitch summation = larger force

28
Q

Frequency of stimulation - Tetanus

A

If there is no time to relax (like me haha :”) ), maximal sustained contraction of Tetanus due to continuous release of Ca2+

29
Q

No. of fibres in recruitment

A
  • Force produced by each fibre depends on no. of fibres activated and the sarcomeres length
30
Q

Length-tension relationship (amount of force produced by each fibre)

A

Each muscle sits at an optimal length n body at rest
*Too stretched, cross bridges can’t occur
* Too slack cause its too contracted, can’t have more contraction of the sarcomeres

31
Q

Recruitment (no. of fibres activated)

A

*force produced by each fibre + no. of fibres activated

No. of fibres activated is regulated by how many neurons activated at one time
Process of activating more motor units is recruitment = more force