Manabe N
Department of Anesthesiology and Rescusitology, Okayama University Medical School, Japan.
Acta Med Okayama. 1997 Feb;51(1):13-8. doi: 10.18926/AMO/30806.
The effect of various non-depolarizing neuromuscular blocking agents (gallamine, pancuronium, vecuronium, d-tubocurarine, metocurine, atracurium and pipecuronium) on [3H]acetylcholine release in the response to field electrical stimulation was investigated in vitro in preparations of the guinea pig right atrium. In this preparation, atropine enhanced and oxotremorine, a muscarinic agonist, reduced the release of [3H] acetylcholine. Atropine reversed the inhibitory effect of oxotremorine in a concentration dependent manner, indicating that there is negative feedback modulation of acetylcholine release from the vagal nerve. While pancuronium, gallamine and atracurium enhanced the release of [3H]acetylcholine, d-tubocurarine, metocurine, vecuronium and pipecuronium did not affect it. Pancuronium and gallamine also reduced the inhibitory effect of oxotremorine and the Kd value of pancuronium for muscarinic receptors located on cholinergic nerve terminals was 2.31 microM. These findings indicate that pancuronium and gallamine enhanced the release of acetylcholine from the atrial parasympathetic nerve, probably by inhibiting presynaptic muscarinic receptors.
在豚鼠右心房制备物中,体外研究了各种非去极化神经肌肉阻滞剂(加拉明、泮库溴铵、维库溴铵、d-筒箭毒碱、美索卡明、阿曲库铵和哌库溴铵)对场电刺激反应中[3H]乙酰胆碱释放的影响。在该制备物中,阿托品增强了[3H]乙酰胆碱的释放,而毒蕈碱激动剂氧化震颤素则降低了其释放。阿托品以浓度依赖性方式逆转了氧化震颤素的抑制作用,表明迷走神经乙酰胆碱释放存在负反馈调节。泮库溴铵、加拉明和阿曲库铵增强了[3H]乙酰胆碱的释放,而d-筒箭毒碱、美索卡明、维库溴铵和哌库溴铵则未对其产生影响。泮库溴铵和加拉明还降低了氧化震颤素的抑制作用,泮库溴铵对胆碱能神经末梢上毒蕈碱受体的解离常数(Kd)值为2.31 microM。这些发现表明,泮库溴铵和加拉明可能通过抑制突触前毒蕈碱受体,增强了心房副交感神经乙酰胆碱的释放。