neuromuscular pharmacology Flashcards

1
Q

what innervates skeletal muscle

A

alpha motor neurones with myelinated axons

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2
Q

when does the alpha motor neurone become unmyelinated

A

when the axon divides near the muscle to innervate individual fibres

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3
Q

what makes up a motor unit

A

alpha neurone and number of fibres it innervates

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4
Q

what is the terminal bouton

A

where fine branches end and synapse at neuromuscular junction

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5
Q

what conducts AP’s

A

ACh

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6
Q

how is ACh synthesised in cytoplasm of bouton

A

choline transported to terminal, choline + acetyl CoA by CHAT

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7
Q

how does neuromuscular transmission work presynapse

A

synthesis of ACh, uptake of ACh to synaptic vesicle for concentration and storage, Ca dependent release of ACh from depolarisation by exocytosis, nicotonic ACh receptor activated, ACh terminated by AchE

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8
Q

how does neuromuscular transmission work postsynapse

A

2 ACh’s activate nAChR (glycoproteins with cation pore), ligand gate channels open and Na enters while K leaves, end plate potential reached and causes contraction

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9
Q

how does AchE terminate ACh

A

hydrolyses it to choline + acetate

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10
Q

what is neuromytonia/ Isaac’s syndrome

A

autoimmune against K channel activation resulting in hyper excitability as cell is already slightly depolarised

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11
Q

what are the symptoms of Isaac’s syndrome and how do you treat it

A

cramps, stiffness, twitches - anticonvulsant eg carbamezepine

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12
Q

what is lambert eaton myasthenic syndrome (LEMS)

A

autoimmune against A channels, reduced entry in repolarisation and reduces Ach release

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13
Q

how do you treat LEMS

A

anticholinesterases

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14
Q

what is myasthenia gravis

A

autoimmune neuromuscular disorder where autoantibodies bind with ACh receptors on muscle cells

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15
Q

what is the pathology of myasthenia gravis

A

autoantibodies bind to and unfold ACh receptos, CD4T activates effector Th cells to attack receptor. this blocks ACh binding and transmission

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16
Q

what type of hypersensitivity is myasthenia gravis

A

type II

17
Q

what are the symptoms of myasthenia gravis

A

progressive muscle weakness and fatigue, occular muscles, face usually affected early on

18
Q

what is myasthenia gravis associated with

A

SLE, RA, thyrotoxiocis, thymic tumour (10% cause), thymic hyperplasia, young woman and old men

19
Q

how do you diagnose myasthenia gravis

A

serum anti-AChR IgG antibodies, repetitive nerve stimulation

20
Q

how do you treat myasthenia gravis

A

anti-cholinerterases eg pyridostigmine, immunosuppresants eg steroids and azathioprine, thymectomy

21
Q

what is myasthenic crisis and how do you treat it

A

diaphragm damaged, ventilation, IV immunoglobin, high dose steroids