Neuromuscular blocking
drugs
Need for neuromuscular
blocking drugs
 Improve intubating conditions
 Providing immobility
 Better surgical conditions
Structure of neuromuscular
junction
 Motor neuron
 Axon
 Nerve terminals
 Synaptic cleft
 Post synaptic membrane
Action potential
 Electrical potential inside the cell is
negative
 Depolarization
 Sodium and calcium channels
 All or none response
acetylcholine
 Acetylcholine synthesis
 Receptors
 Vesicles
 Anticholinesterases
 Synaptic cleft
 Calcium and magnesium
Post synaptic events
 Ach receptor
 Ligand gated ion channel
 Structure of the receptor
 Adult ,fetal ,extrajunctional
 acetylcholinesterase
Presynaptic events
 Presynaptic receptor
 Preventing mobilisation of acetylcholine
vesicles
Pharmacologic characteristics
 Potency
 Onset
 duration
atracurium
 Hoffman reaction
 Nonspecific ester hydrolysis
 Dose 0.5 mg/kg
 Onset 3 -5 min
 Duration 30 – 45 min
Specific points
 Histamine release
 Intubating dose
 Maintenance of anaesthesia
 Can be used in patients with hepatic or
renal failure
cisatracurium
 Dose 0.1 mg/kg
 Duration 30 -45 min
 Devoid of histamine releasing properties
mivacurium
 Short acting
 Degraded by plasma esterases
 0.3. mg/kg
 Ambulatory and laprascopic surgery
pancuronium
 Increase heart rate,blood pressure and
cardiac output
 Sympathomimetic effect
 Duration of action 1 hr
 Higher incidence of muscular weakness
after cardiac surgery than rocuronium
rocuronium
 0.6 mg/kg intubating dose
 Duration 30 -40 min
 No hemodynamic effects
 Rapid sequence induction
 sugammadex
vecuronium
 Intubating dose 0.1 mg/kg
 No cardiovascular effects
 Excreted by the kidney
 Intermediate duration of action
 Precipitates with thiopentone
neostigmine
 Reversible anticholinesterase inhibitor
 50 -70 mcg/kg
 Increased acetylcholine in the receptor
 Profound vagal stimulation
 Administered with glycopyrrolate or
atropine
sugammadex
 Gamma cyclodextrin
 Steroid nucleus –rocuronium and
vecuronium
 No cardiovascular adverse effects
 16 mg/kg dose required
Special considerations
 Myasthenia gravis
 Myotonia
 Burns
 Muscular dystrophy
 UMN lesions

neuromuscular blocking agents