NMJ and Muscle contraction Flashcards

1
Q

What is a neuromuscular junction?

A

Specialised structure incorporating the distal exon terminal and muscle membrane that allows for unidirectional chemical communication between peripheral nerve and muscle

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2
Q

What is a synapse?

A

Allows unidirectional flow

Contact ratio varies from 1:1 in muscle and 10^3:1 in the CNS

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3
Q

What enzyme breaks down acetylcholine?

A

Acetylcholinesterase

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4
Q

What are 3 points of failure of the neuromuscular junction?

A

Demyelination
Loss of ACHesterase
Faulty VGCCs

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5
Q

What happens in demyelination?

A

Reduced conduction velocity

Weak/uncoordinated muscle movement

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6
Q

Where does the upper motor neurone go?

A

in the brain

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7
Q

Where does the lower motor neurone do?

A

in brainstem if to face

in spinal chord if to elsewhere

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8
Q

What do motor neurones to effectors look like

A

Soma in butterfly shaped grey matter
Surrounded by white matter and tracts
With axons that leave the anterior ventral horn

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9
Q

How many neurone branches does each muscle fibre receive?

A

One

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10
Q

What happens if a muscle is reinnervated by a damaged nerve?

A

Then the muscle can have branches form multiple neurones and be innervated by branches from previously unconnected nerves

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11
Q

What happens in the synapse in normal physiology?

A

AP opens VGCC causing Ca2+ influx
Ca2+ influx triggers vesicles exocytosis so ACh diffuses into the cleft and binds to receptor cation channels, opening these on the post synaptic neurone
Local currents flow from depolarised region and adjacent region, triggering an AP
ACh broken down by acetylcholinesterase and muscle fibre response ceases

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12
Q

What happens in synapses at rest?

A

Individual vesicles release ACh at low rate causing minature end plate potentials (MEPPs)

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13
Q

Voluntary or involuntary control?
Smooth muscle
Skeletal muscle
Cardiac muscle

A

Smooth muscle: involuntary - around round organs eg GI tract and vessels
Skeletal muscle: voluntary - allow for limb/body movement
Cardiac muscle: involuntary - cause myocardial contraction

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14
Q

What is the structure of myofibre?

A

Covered by sarcolemma plasma membrane with t-tubules tunnelling to centre, and a sarcoplasm (cytoplasm) with myoglobulin and mitochondria present.

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15
Q

What is the sarcoplasmic reticulum?

A

Network of fluid filled tubules that store Ca2+ ions

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16
Q

What do myofibrils look like?

A

1-2um diameter extending along entire length of myofibres, composed of actin and myosin (and other proteins)

17
Q

What do myofilaments look like?

A

Straited due to light and dark bands
Do not extend along whole length of myofibres
Overlap and arranged into compartments called sarcomeres (Z-Z)

18
Q

What happens in eccentric muscle contraction?

A

Muscle gets longer during contraction
Painful
Can lead to shearing and ripping out tendons/muscles

19
Q

What happens in concentric muscle contraction

A

Muscle shortens during contraction

20
Q

What happens in relaxation of muscle?

A

Ca2+ dissociates from troponin when free Ca2+ declines
Preventing new crossbridges forming
Ca2+ actively transported back to SR during AP so for contraction release => return

21
Q

What are examples of NMJ disorders?

A

Botulism
Myasthenia Gravis
Lambert Eaton myasthenic syndrome

22
Q

What happens in botulism disorder?

A

Botulism toxin leads to irrevocable disruption in stimulation induced ACh release by presynaptic nerve terminal

23
Q

What happens in myasthenia gravis disorder?

A

Autoimmune disorder leading to Ab production against ACh receptors causing fatigable weakness -
affect ocular, bulbar (brainstem), respiratory or limb muscles - confirmed by EMG; may need plasma exchange/AChesterase inhibitors

24
Q

What happens in Lambert-Eaton myasthenic syndrome? (LEMS)

A

Autoimmune Ab production against VGCCs associated with lung cancer, may need ACh analogue

25
Q

What is corticobulbar

A

Cortex to brainstem to muscles of the face = preferentially affected by MG

26
Q

What is corticospinal?

A

Cortex to spinal chord to muscles of the body