ACTIVATION OF BRAIN ACETYLCHOLINE-RECEPTORS BY NEUROMUSCULAR BLOCKING-DRUGS - A POSSIBLE MECHANISM OF NEUROTOXICITY

Background: Neuromuscular blocking drugs cause excitement and seizures when introduced into the central nervous system. We examined the possibility that these drugs produce paradoxical activation of acetylcholine or glutamate receptors, the chief types of brain receptors involved in excitatory neurotransmission. Methods: Because activation of central glutamate or acetylcholine receptors causes calcium influx into postsynaptic neurons, we measured intracellular calcium concentration ([Ca2+](i)) as an index of receptor activation. Changes in [Ca2+](i) were compared in brain slices exposed to neuromuscular blocking drugs or acetylcholine and glutamate receptor agonists. [Ca2+](i) was measured with the fluorescent dye fura-2. Results: Pancuronium and vecuronium caused sustained increases in [Ca2+](i) in approximately the same potency ratio as for seizure activity in vivo (concentrations at which the increase in [Ca2+](i) was 95% of maximal: 100 and 400 mu M, respectively). Atracurium and laudanosine did not increase [Ca2+](i) in cortical slices. Increases in [Ca2+](i) caused by both pancuronium and vecuronium were prevented by the non-subtype-specific nicotinic acetylcholine receptor antagonist D-tubocurarine and were reduced 44-73% by atropine. Blockade of glutamate receptors or voltage-gated calcium or sodium channels had no effect on calcium influx. Conclusions: The results suggest that the acute excitement and seizures caused by introduction of pancuronium and ve curonium into the central nervous system is due to accumulation of cytosolic calcium caused by sustained activation of acetylcholine receptor ion channels.