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酯类和酮类的麻醉作用:鱿鱼轴突中与钠通道蛋白相互作用的证据。

Anaesthetic action of esters and ketones: evidence for an interaction with the sodium channel protein in squid axons.

作者信息

Elliott J R, Haydon D A, Hendry B M

出版信息

J Physiol. 1984 Sep;354:407-18. doi: 10.1113/jphysiol.1984.sp015384.

Abstract

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.

摘要

已研究了甲基丁基酮、甲基庚基酮和甲基戊酸酯对乌贼巨轴突钠电流的影响。每种物质均可使完整轴突中的内向电流峰值可逆性降低。在细胞内灌注的轴突中,于暴露于受试物质之前及期间记录钠电流,并将记录结果与霍奇金和赫胥黎(1952年)提出的方程进行拟合。这些物质引起的稳态激活和失活参数(m无穷大与h无穷大)的电压依赖性变化、激活和失活时间常数(τm和τh)峰值高度的降低以及最大钠电导(gNa)的变化已制成表格,并与甲基辛酸酯的作用进行了比较(海登和厄本,1983b)。每种化合物均使稳态失活参数的电压依赖性向超极化方向移动,而使稳态激活参数的电压依赖性向去极化方向移动。将酮类产生的变化与甲基戊酸酯和甲基辛酸酯产生的变化进行了比较。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无穷大位移方面可能发挥的作用。峰值时间常数降低,τm和τh的电压依赖性朝着与稳态特性变化相称的方向移动。酮类和甲基戊酸酯对最大钠电导的影响均不大。对于正链烷醇和其他表面活性化合物,已报道内向电流峰值大幅降低,而对gNa影响很小(海登和厄本,1983b)。对gNa缺乏较大影响表明,无论受试物质与通道蛋白之间发生何种直接相互作用,均不会导致通道堵塞。

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