4 - The NMJ and muscle contraction Flashcards

1
Q

Define the neuromuscular junction

A

a specialised synapse between a motor neurone and a muscle fibre

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2
Q

What are the structures involved in a NMJ?

A

presynaptic nerve terminal
synaptic cleft
post endplate region of the muscle fibre

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3
Q

What is the neurotransmitter for voluntary striated muscle?

A

acetylcholine

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4
Q

What are the fibres coming out of the anterior and posterior roots of the spinal cord?

A

ventral root - motor fibres

dorsal root - sensory fibres

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5
Q

Where are the cell bodies of the sensory and motor neurones?

A

motor neurone cell bodies - in they grey matter of the spinal chord
sensory neurone cell bodies - in the dorsal root ganglia

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6
Q

What are the NMJ between specifically?

A

the axons terminal and the muscle fibres

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7
Q

Give the 7 stages of initiating muscle contraction at the NMJ

A

1 - Action potential open V-gated Ca2+ channels
2 - Ca2+ enters
3 - Ca2+ triggers exocytosis of vesicles
4 - Acetylcholine diffuses in cleft
5 - Acetylcholine binds to receptor-cation channel & opens channel
6 - Local currents flow from depolarized region and adjacent region; action potential triggered and spreads along surface membrane
7 - Acetylcholine broken down by acetylcholine esterase (enzyme). Muscle fibre response to that molecule of Acetylcholine ceases

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8
Q

What are MEPPs?

A

miniature end-plate potentials

individual vesicles releasing ACh at very low rates - they are cause by slight depolarisations

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9
Q

Give the layers of of skeletal muscle and what they are wrapped in

A
  • muscle fibers (the muscle cells) are surrounded by endomysium
  • muscle fibres are bundled together to form fasiculata
  • fasiculata is bounded by perimysium
  • the muscle is surrounded by epimysium
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10
Q

Give the microstructure of a muscle fibre

A

each muscle fibre is a cell containing myofibrils and many nuclei
- the myofibrils have capillaries running along their surface and indentations of the sarcolemma called t-tubules. The sarcoplasm has myoglobin and mitochondria present in it

  • myofilaments are the single thread-like structures found in myofibrils. Comprised of actin and myosin. They are the structural unit of myofibrils. They extend along the entire length of myofibres. They have striated appearance.
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11
Q

What happens to the light and dark bands during contractions of skeletal muscles?

A
  • I band becomes shorter
  • A band remains the same length
  • H zone narrows and disappears
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12
Q

Activation and relaxation process

A

1 - Action potential propagates along surface membrane and into T-tubules
2 - DHP (dihydropyridine) receptor in T-tubule membrane: senses V & changes shape of the protein link to Ryanodine receptor, opens the Ryanodine receptor Ca2+ channel in the SR membrane; Ca2+ released from SR into space around the filaments
3 - Ca2+ binds to Troponin & Tropomyosin moves allowing 4 - Crossbridges to attach to actin
5 - Ca2+ is actively transported into the SR continuously while action potentials continue. ATP- driven pump (uptake rate < or = release rate).
6 - Ca2+ dissociates from TN when free Ca2+ declines; TM block prevents new crossbridge attachment; Active force declines due to net crossbridge detachment

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13
Q

Give 3 disorders that arise as a result of pathological processes interfering with NMJ function and causing muscle weakness

A
  • botulism
  • myastenia gravis
  • LEMS (Lambert-Eaton myastenic syndrome)
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14
Q

How does NMJ disfunction cause botulism?

A

the botulism toxin produces an irreversible disruption in stimulation-induced ACh release by presynaptic nerve terminal
prevents calcium influx into presynaptic nerve

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15
Q

What is myasthenia gravis?

A

an autoimmune disease
antibodies are directed against the acetylcholine receptor, block the receptors so ACh cannot bind

causes fatiguable weakness
affects muscle of the face and eyes: droopy eyelids, lack of facial muscle movement

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16
Q

What is Lambert-Eaton myastenia syndrome?

What condition is it associated with?

A

an autoimmune disease
cause by antibodies directed against VGCC - failure of Ca2+ channels and, hence, neurotransmission

associated with lung cancer

17
Q

What does myasthenia mean?

A

serious muscle weakness