首页> 美国卫生研究院文献>The Journal of Physiology >Anaesthetic action of esters and ketones: evidence for an interaction with the sodium channel protein in squid axons.
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Anaesthetic action of esters and ketones: evidence for an interaction with the sodium channel protein in squid axons.

机译:酯和酮的麻醉作用:与鱿鱼轴突中钠通道蛋白相互作用的证据。

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摘要

The effects of methyl butyl ketone, methyl heptyl ketone and methyl pentanoate on the sodium current of the squid giant axon have been examined. The peak inward current in intact axons was reduced reversibly by each substance. Sodium currents were recorded in intracellularly perfused axons before and during exposure to the test substances and the records were fitted with equations similar to those proposed by Hodgkin & Huxley (1952). Shifts in the voltage dependence of the steady-state activation and inactivation parameters (m infinity and h infinity), reductions in the peak heights of the activation and inactivation time constants (tau m and tau h) and changes in the maximum sodium conductance (gNa) caused by these substances have been tabulated and compared with the effects of methyl octanoate (Haydon & Urban, 1983b). Each compound shifted the voltage dependence of the steady-state inactivation parameter in the hyperpolarizing direction and that of the steady-state activation parameter in the depolarizing direction. The shifts produced by the ketones are compared with those produced by methyl pentanoate and by methyl octanoate. The possible role of an interaction between the carbonyl oxygen of the test substance and the sodium channel protein in producing the h infinity shift is discussed. The peak time constants are reduced and the voltage dependences of tau m and tau h are shifted in a direction commensurate with the shifts in steady-state properties. The maximum sodium conductance is not much affected either by the ketones or by methyl pentanoate. Large reductions in peak inward current coupled with little effect on gNa have been reported for the n-alkanols and other surface-active compounds (Haydon & Urban, 1983b). This lack of a large effect on gNa indicates that whatever direct interaction does take place between the test substance and the channel protein, it does not result in a blockage of the channel.
机译:研究了甲基丁基酮,甲基庚基酮和戊酸甲酯对鱿鱼巨轴突钠电流的影响。每种物质均会可逆地减少完整轴突的最大内向电流。在暴露于测试物质之前和之中,在细胞内灌注的轴突中记录了钠电流,并且该记录符合类似于Hodgkin&Huxley(1952)提出的方程式。稳态激活和失活参数的电压依赖性(m无穷大和h无穷大)的变化,激活和失活时间常数的峰值高度(tau m和tau h)的减小以及最大钠电导(gNa)的变化将这些物质引起的)列表并与辛酸甲酯的影响进行了比较(Haydon&Urban,1983b)。每种化合物在超极化方向上偏移稳态失活参数的电压依赖性,而在去极化方向上偏移稳态激活参数的电压依赖性。将酮产生的位移与戊酸甲酯和辛酸甲酯产生的位移进行比较。讨论了受试物质的羰基氧与钠通道蛋白之间的相互作用在产生h无穷大位移中的可能作用。峰值时间常数减小,并且tau m和tau h的电压相关性在与稳态特性变化相对应的方向上变化。钠或戊酸甲酯对钠的最大电导率影响不大。对于正链烷醇和其他表面活性化合物,已经报道了最大的内向峰值电流减小而对gNa的影响很小(Haydon&Urban,1983b)。缺少对gNa的大影响表明,无论测试物质与通道蛋白之间发生了什么直接相互作用,都不会导致通道阻塞。

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