NMJ and EMG Flashcards

1
Q

what is a neuromuscular junction?

A

synapse between motor neurone and muscle fibre

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2
Q

difference between synapse and NJM

A

Nerve terminal bouton releases acetylcholine into the synaptic cleft, and binds to acetylcholine receptors (nicotinic) on the post synaptic endplate, which has junctional folds.

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3
Q

what is a motor unit?

A

one motor neurone branches to form many junctions with many muscle fibres.

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4
Q

where is acetylcholinesterase found?

A

on the end plate membrane, it breaks down Ach to stop its effects.

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5
Q

what are miniature end plate potentials (EPPs)?

A

at rest there is a small amount of acetylcholine still released due to intracellular calcium.

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6
Q

describe the structure of skeletal muscle

A

one muscle fibre cell is surrounded by the endomysium, a group of these muscle fibres is called a fascicle surrounded by a perimysium. a group of fascicles make up the muscle itself which is surrounded by an epimysium.

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7
Q

what is in the sarcoplasm?

A

T tubules of the sarcolemma, network of Sarcoplasmic Reticulum, myoglobin, myofibrils, mitochondria.

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8
Q

how wide are myofibrils?

A

1-2um

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9
Q

what is the A band?

A

Dark Bands of myosin that are a constant width after contraction.

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10
Q

what is the I band?

A

light bands of actin that decreases when contraction occurs.

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11
Q

what is the H zone?

A

Area in the middle of the A band that gets smaller when contraction occurs.

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12
Q

why is ATP always used even when muscle relaxed?

A

SER continuously pumps calcium back in, even when contraction occurs.

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13
Q

what is Botulism?

A

botulinum toxin produced by pathogen which causes irreversible release of Ach from presynaptic terminal this leads to paralysis

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14
Q

what is Myastenia Gravis (MG)?

A

autoimmune disorder against Ach Receptor this leads to muscle weakness

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15
Q

what is Lambert-Eaton Myastenic Syndrome (LEMS)?

A

associated with lung cancer, autoimmune diseases against VGCCs.

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16
Q

what is an EMG?

A

electromyography, extracellular reading of action potentials that govern skeletal muscle contraction.

17
Q

how does an EMG work?

A

two extracellular probes places apart on the skin which is positively charges when the muscles beneath are at resting potential (-70mV). As an AP moves along, the first probe will be in a negative region and the second will be in the positive region hence a potential difference is measured. When this AP moves along to the second probe, the second probe will detect a negative current and the first probe will detect a positive current causing the potential difference to flip.

18
Q

as the force of muscle contraction increases, what happens to the EMG peaks?

A

frequency and amplitude increases.

19
Q

as you increase the magnitude of stimulus provided to the muscle (eg adductor pollicis) what happens to twitch force?

A

increases

20
Q

As you increase frequency of stimulus, what happens to the twitch force?

A

at first you increase the frequency of twitching, then there is summation of force, then at higher frequencies there is tetanus.

21
Q

why are EMGs clinically important?

A

helps distinguish between myopathies and neuropathies.