Skeletal muscle relaxants acting on the NMJ Flashcards
Name the non-depolarising skeletal muscle relaxants?
Competitive antagonists of Nm
- Isoquinolines
D-tubocurarine Mivacurium Cistracurium Atracurium Doxacurium
Which non-depolarising SM relaxant is metabolised by Pseudocholinesterase?
Mivacurium
How are Cistracurium and Atracurium metabolised?
Spontaneous (Hoffmann-elimination)
Which non-depolarising skeletal muscle relaxants are metabolised spontaneously?
Cistracurium and atracurium
What is the duration of action of Mivacurium?
Short acting (10-15 mins)
What is the duration of action of Cistracurium?
Intermediate acting (20-30 mins)
What is the duration of action of Atracurium?
Intermediate acting (15-35 mins)
What is the duration of action of Doxacurium?
Long acting
What is the duration of action of D-tubocurarine?
> 35 mins
Which drug is safe in renal and hepatic impairment?
Why?
Atracurium
Because it is spontaneously inactivated to Laudonosine (therefore does not use the liver or kidneys in its metabolism)
What is the break down product of Atracurium?
Laudonosine
In which patients do we not use Mivacurium?
In those who are quick metabolisers (pseudocholinesterase). It already has a short duration of action.
How do you reverse the block induced by non-depolarising SM relaxants?
Competitive non depolarising SM relaxants are competitive so you over come the effects by increasing the concentration of the ligand of the receptor; in this case, Ach - so you use an AchE inhibitor.
You use Neostigmine (quartenary AchE inhibitor) - cannot enter the CNS.
Not physostigmine as it is a tertiary amine and can enter the CNS
Not Edrophonium as it has a short half life.
Name the non-depolarising SM relaxants?
Steroids
Vecuronium
Rocuronium
Pancuronium
Pipecuronium
Which non depolarising SM relaxants are metabolised by the Liver?
Vecuronium
Rocuronium