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美洲大蠊轴突钠通道的药理学特性。I. 合成石房蛤毒素的选择性阻断

Pharmacological properties of axonal sodium channels in the cockroach Periplaneta americana L. I. Selective block by synthetic saxitoxin.

作者信息

Sattelle D B, Pelhate M, Hue B

出版信息

J Exp Biol. 1979 Dec;83:41-8. doi: 10.1242/jeb.83.1.41.

Abstract

Voltage-clamp experiments on isolated giant axons of the cockroach Periplaneta americana L. show that chemically synthesized saxitoxin specifically and reversibly blocks the transient inward sodium current without affecting the steady-state outward potassium current. From the concentration depending of sodium current suppression it is concluded that individual sodium channels are blocked by single molecules of synthetic saxitoxin which bind reversibly to part of the channel with a dissociation constant of 3.0 x 10(-9) M. Synthetic saxitoxin blocks sodium channels in cockroach axons at a lower concentration than tetrodotoxin. Sodium channel block by synthetic saxitoxin is more readily reversed than tetrodotoxin-induced block.

摘要

对美洲大蠊孤立的巨轴突进行的电压钳实验表明,化学合成的石房蛤毒素能特异性且可逆地阻断瞬时内向钠电流,而不影响稳态外向钾电流。从钠电流抑制的浓度依赖性可以得出结论,单个钠通道被单个合成石房蛤毒素分子所阻断,这些分子以3.0×10⁻⁹ M的解离常数可逆地结合到通道的一部分。合成石房蛤毒素比河豚毒素以更低的浓度阻断蟑螂轴突中的钠通道。与河豚毒素诱导的阻断相比,合成石房蛤毒素对钠通道的阻断更容易逆转。

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