Huneeus-Cox F, Fernandez H L, Smith B H
Biophys J. 1966 Sep;6(5):675-89. doi: 10.1016/S0006-3495(66)86686-9.
The effects of internally and externally applied sulfhydryl reagents on the bioelectric properties of the giant axon of the squid Loligo pealeii and Dosidicus gigas were studied. Cysteine-HCl (400 mM, pH 7.3) was used to remove axoplasm from the perfusion channel. Oxidizing agents (1 to 60 mM) tended to increase the duration of the action potential and had a slow, irreversible blocking effect when perfused internally; the membrane potential was little affected. Reducing agents applied internally caused a decrease in the spike duration without affecting its height or the membrane potential, although at high concentrations there was reversible deterioration of the action potential. Both external and internal perfusion of mercaptide-forming reagents caused deterioration in the action and membrane potentials with conduction block occurring in 5 to 45 min. 2-mercaptoethanol reversed the effects. Thiol alkylating reagents, iodoacetate and iodoacetamide, were without effect. N-ethylmaleimide did, however, block. Tests with chelating agents for nonheme iron in the membrane brought about no change in the electrical parameters. The implications of the present findings with regard to the macromolecular mechanism of excitation are discussed.
研究了内源性和外源性巯基试剂对鱿鱼(Loligo pealeii和Dosidicus gigas)巨大轴突生物电特性的影响。使用盐酸半胱氨酸(400 mM,pH 7.3)从灌注通道中去除轴浆。氧化剂(1至60 mM)倾向于增加动作电位的持续时间,当内部灌注时具有缓慢、不可逆的阻断作用;膜电位受影响较小。内部应用还原剂会导致峰电位持续时间缩短,而不影响其高度或膜电位,尽管在高浓度时动作电位会出现可逆性恶化。形成硫醇盐的试剂进行外部和内部灌注都会导致动作电位和膜电位恶化,并在5至45分钟内发生传导阻滞。2-巯基乙醇可逆转这些效应。硫醇烷基化试剂碘乙酸盐和碘乙酰胺无效。然而,N-乙基马来酰亚胺确实会产生阻断作用。用膜中与非血红素铁结合的螯合剂进行测试,电参数没有变化。讨论了本研究结果对兴奋的大分子机制的意义。