Gardier R W, Tsevdos E J, Jackson D B
J Pharmacol Exp Ther. 1978 Jan;204(1):46-53.
Pancuronium enhanced contraction of the nictitating membrane elicited via ganglionic muscarinic pathways in the superior cervical ganglion of the cat. In order to elucidate this phenomenon, recordings of the superior cervical ganglion surface potential were made which demonstrated that pancuronium and gallamine reduced and haloperidol enhanced ganglionic hyperpolarization without significantly altering the ganglionic slow depolarization. Pancuronium reversed the effects produced by haloperidol, whereas the latter drug was unable to antagonize those induced by pancuronium. These results allow the speculation that pharmacologically distinct muscarinic receptors reside in sympathetic ganglia, one of which is susceptible to blockade by pancuronium or gallamine.
泮库溴铵增强了通过猫颈上神经节中的神经节毒蕈碱途径引发的瞬膜收缩。为了阐明这一现象,对颈上神经节表面电位进行了记录,结果表明泮库溴铵和加拉明降低了神经节超极化,氟哌啶醇增强了神经节超极化,而对神经节缓慢去极化没有显著影响。泮库溴铵逆转了氟哌啶醇产生的作用,而后者药物无法拮抗泮库溴铵诱导的作用。这些结果使人推测,药理学上不同的毒蕈碱受体存在于交感神经节中,其中一种易受泮库溴铵或加拉明的阻断。