HOSKIN F C, ROSENBERG P
J Gen Physiol. 1964 Jul;47(6):1117-27. doi: 10.1085/jgp.47.6.1117.
Choline and neostigmine markedly antagonize the effect of acetylcholine (ACh) on the action potential of the venom-treated squid axon, although they themselves have no effect on conduction. Physostigmine also antagonizes the blocking action of ACh at a concentration well below that which has any effect on conduction. In contrast, d-tubocurarine (curare) increases the effect of ACh on the action potential. Choline, neostigmine, and physostigmine markedly decrease the penetration of C(14)-labeled ACh into the axoplasm of the squid axon. Curare, in contrast, increases the penetration of ACh, whereas dimethylcurare gives variable results. The results provide an explanation why physostigmine and neostigmine do not influence the action of ACh on axonal conduction in a way similar to that observed at the junction. The additive effect of curare and ACh on the action potential may be due either to the greater rate of penetration of ACh or to an additive effect of the two compounds on the receptor, or to a combination of both factors.
胆碱和新斯的明能显著拮抗乙酰胆碱(ACh)对经毒液处理的乌贼轴突动作电位的影响,尽管它们本身对传导没有影响。毒扁豆碱在远低于对传导有任何影响的浓度下也能拮抗ACh的阻断作用。相比之下,d -筒箭毒碱(箭毒)会增强ACh对动作电位的影响。胆碱、新斯的明和毒扁豆碱能显著降低C(14)标记的ACh进入乌贼轴突轴浆的渗透率。相反,箭毒会增加ACh的渗透率,而二甲基箭毒的结果则各不相同。这些结果解释了为什么毒扁豆碱和新斯的明对ACh在轴突传导上的作用的影响方式,与在神经肌肉接头处观察到的情况不同。箭毒和ACh对动作电位的相加作用可能是由于ACh的渗透率更高,或者是这两种化合物对受体的相加作用,或者是这两个因素的综合作用。