Vercruysse P, Bossuyt P, Verbeuren T J, Vanhoutte P M, Hanegreefs G
Acta Anaesthesiol Belg. 1979;30 Suppl:71-8.
The influence of gallamine, pancuronium, d-tubocurarine and succinylcholine on adrenergic neurotransmission was studied in the isolated saphenous vein of the dog. Pancuronium increased the response of vascular smooth muscle to adrenergic nerve stimulation and to exogenous norepinephrine; gallamine, d-tubocurarine and succinylcholine had no effect. The relaxation caused by small doses of acetylcholine added during sympathetic nerve stimulation (prejunctional effect), was inhibited by pancuronium and by gallamine. In vein strips, charged with (3H) norepinephrine, acetylcholine inhibits the catecholamine-efflux evoked by sympathetic nerve stimulation. That inhibition was abolished by gallamine. This confirms that gallamine inhibits the prejunctional effect of acetylcholine on adrenergic neurotransmission. When extrapolated to the intact organism, this means that gallamine and pancuronium will augment the release of norepinephrine by acting as muscarinic antagonists also at prejunctional receptor sites in tissues exposed to combined sympathetic and vagal nerve activity. This mechanism would explain in part the cardiovascular effects of these muscle relaxants.
在犬离体隐静脉中研究了加拉明、泮库溴铵、d -筒箭毒碱和琥珀酰胆碱对肾上腺素能神经传递的影响。泮库溴铵增强了血管平滑肌对肾上腺素能神经刺激和外源性去甲肾上腺素的反应;加拉明、d -筒箭毒碱和琥珀酰胆碱则无此作用。在交感神经刺激期间添加小剂量乙酰胆碱所引起的舒张作用(接头前效应),被泮库溴铵和加拉明抑制。在装载有(3H)去甲肾上腺素的静脉条中,乙酰胆碱抑制交感神经刺激所诱发的儿茶酚胺外流。该抑制作用被加拉明消除。这证实加拉明抑制乙酰胆碱对肾上腺素能神经传递的接头前效应。外推至完整机体时,这意味着加拉明和泮库溴铵通过在交感神经和迷走神经联合活动的组织中的接头前受体部位充当毒蕈碱拮抗剂,将增强去甲肾上腺素的释放。这一机制将部分解释这些肌肉松弛剂的心血管效应。