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一种自旋标记局部麻醉剂对鱿鱼轴突膜的离子作用机制。

Ionic mechanism of action of a spin-labeled local anesthetic on squid axon membranes.

作者信息

Yeh J Z, Takeno K, Rosen G M, Narahashi T

出版信息

J Membr Biol. 1975;25(3-4):237-47. doi: 10.1007/BF01868577.

Abstract

The ionic mechanism of action of a spin-labeled local anesthetic (SLA), 2-[N-methyl-N-(2,2,6,6-tetramethylpiperidonooxyl)]-ethyl 4-ethoxylbenzoate, was studied by means of voltage clamp technique with squid giant axons in comparison with the parent compound without spin label moiety, 2-(N,N-dimethyl)ethyl 4-ethoxylbenzoate (GS-01). Like other local anesthetics, they suppressed both sodium and potassium conductance increases. However, three remarkable differences have been noted between SLA and GS-01: (1) SLA is more effective than GS-01 in suppressing the sodium and potassium conductance increases; (2) SLA induces a potassium inactivation, whereas GS-01 is lacking this ability; (3) SLA has no effect on the time to peak sodium current, whereas GS-01 prolongs it. GS-01 resembles procaine with respect to (2) and (3) above. SLA will become a useful probe for the study of the molecular mechanism of local anesthetic aciton and of ionic channel function.

摘要

通过乌贼巨轴突的电压钳技术,对一种自旋标记的局部麻醉剂(SLA),即2-[N-甲基-N-(2,2,6,6-四甲基哌啶氮氧自由基)]-乙基4-乙氧基苯甲酸酯的离子作用机制进行了研究,并与没有自旋标记部分的母体化合物2-(N,N-二甲基)乙基4-乙氧基苯甲酸酯(GS-01)作了比较。与其他局部麻醉剂一样,它们都抑制了钠电导和钾电导的增加。然而,在SLA和GS-01之间发现了三个显著差异:(1)在抑制钠电导和钾电导增加方面,SLA比GS-01更有效;(2)SLA可诱导钾失活,而GS-01缺乏这种能力;(3)SLA对钠电流峰值时间没有影响,而GS-01会延长该时间。就上述(2)和(3)而言,GS-01与普鲁卡因相似。SLA将成为研究局部麻醉作用分子机制和离子通道功能的有用探针。

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