Galindo A, Kelly P J
Anesth Analg. 1980 Jul;59(7):484-7.
The mechanisms of action of gallamine on nerve terminals, cholinergic receptors, and the threshold for propagation of end-plate potentials to the muscle fiber were investigated in rat phrenic nerve-diaphragm preparations. Intracellular studies were made with glass microelectrodes to determine changes in end-plate potentials and miniature end-plate potentials produced by gallamine at concentrations between 10(-7) M to 10(-4) M. Gallamine excited and then depressed the release of transmitter from nerve terminals. This effect was clearly seen at rapid rate of stimulation and during studies of refractoriness using paried stimulation tests. Gallamine had no significant effects on the electrogenic properties of the excitable membranes of motor nerve terminals and muscle fibers; this compound depressed the response of postsynaptic receptors to action of acetylcholine as seen by the reduction in miniature end-plate potentials amplitude. Reduction in muscle twitch was caused solely by failure of propagation of end-plate potentials as muscle action potentials.
在大鼠膈神经 - 膈肌标本中,研究了加拉明对神经末梢、胆碱能受体以及终板电位向肌纤维传播阈值的作用机制。使用玻璃微电极进行细胞内研究,以确定加拉明在10(-7)M至10(-4)M浓度范围内产生的终板电位和微小终板电位的变化。加拉明先兴奋然后抑制神经末梢递质的释放。在快速刺激速率下以及使用配对刺激试验研究不应期时,这种效应清晰可见。加拉明对运动神经末梢和肌纤维的可兴奋膜的电生特性没有显著影响;该化合物通过微小终板电位幅度的降低,抑制了突触后受体对乙酰胆碱作用的反应。肌肉抽搐的减少完全是由于终板电位作为肌肉动作电位传播失败所致。