Waud B E, Waud D R
Anesthesiology. 1985 Jul;63(1):4-15. doi: 10.1097/00000542-198507000-00002.
The influence of gallamine, metocurine, pancuronium, and tubocurarine on depolarization of a mammalian muscle end-plate region was examined to determine whether the antagonists given in combination exerted a degree of block consistent with the simple classical competitive model. Depolarization was produced by carbachol in isolated guinea pig lumbrical muscles and recorded by the moving fluid electrode technique. The dose-response values obtained were fitted to a regression embedded in a split plot factorial experimental design such as both to control and to measure effects of variation among preparations, order of administration, time, and level of block. Of the six possible pairings of the four drugs, four showed the simple additivity expected from a competitive mechanism, while two (pancuronium plus metocurine and metocurine plus gallamine) showed potentiation beyond additivity. In these latter two pairs the combination shifted the carbachol dose-response curve, respectively, 41 and 21% further than predicted from the classical model. The significance of this deviation in the light of alternative receptor models is discussed, and a model consistent with the observed results is outlined.
研究了加拉明、美索卡林、泮库溴铵和筒箭毒碱对哺乳动物肌肉终板区去极化的影响,以确定联合使用这些拮抗剂是否产生了与简单经典竞争模型相符的阻滞程度。在分离的豚鼠蚓状肌中,用卡巴胆碱产生去极化,并通过移动流体电极技术进行记录。将获得的剂量反应值拟合到析因实验设计中的回归模型中,以控制和测量不同标本、给药顺序、时间和阻滞水平的变化影响。在这四种药物的六种可能配对中,四种表现出竞争机制预期的简单相加性,而两种(泮库溴铵加美索卡林和美索卡林加加拉明)表现出超过相加性的增强作用。在这后两种配对中,联合用药使卡巴胆碱剂量反应曲线分别比经典模型预测的进一步偏移了41%和21%。根据其他受体模型讨论了这种偏差的意义,并概述了一个与观察结果一致的模型。