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河豚毒素对钠通道阻滞的使用依赖性:俘获离子机制的复兴。

Use dependence of tetrodotoxin block of sodium channels: a revival of the trapped-ion mechanism.

作者信息

Conti F, Gheri A, Pusch M, Moran O

机构信息

Istituto di Cibernetica e Biofisica, CNR, Genoa, Italy.

出版信息

Biophys J. 1996 Sep;71(3):1295-312. doi: 10.1016/S0006-3495(96)79330-X.

Abstract

The use-dependent block of sodium channels by tetrodotoxin (TTX) has been studied in cRNA-injected Xenopus oocytes expressing the alpha-subunit of rat brain IIA channels. The kinetics of stimulus-induced extra block are consistent with an underlying relaxation process involving only three states. Cumulative extra block induced by repetitive stimulations increases with hyperpolarization, with TTX concentration, and with extracellular Ca2+ concentration. We have developed a theoretical model based on the suggestion by Salgado et al. that TTX blocks the extracellular mouth of the ion pore less tightly when the latter has its external side occupied by a cation, and that channel opening favors a tighter binding by allowing the escape of the trapped ion. The model provides an excellent fit of the data, which are consistent with Ca2+ being more efficient than Na+ in weakening TTX binding and with bound Ca2+ stabilizing the closed state of the channel, as suggested by Armstrong and Cota. Reports arguing against the trapped-ion mechanism are critically discussed.

摘要

河豚毒素(TTX)对钠通道的使用依赖性阻断已在注射了编码大鼠脑IIA通道α亚基的cRNA的非洲爪蟾卵母细胞中进行了研究。刺激诱导的额外阻断动力学与仅涉及三种状态的潜在松弛过程一致。重复刺激诱导的累积额外阻断随超极化、TTX浓度和细胞外Ca2+浓度增加。我们基于Salgado等人的建议开发了一个理论模型,即当离子孔的外侧被阳离子占据时,TTX对离子孔细胞外侧的阻断较松,并且通道开放通过允许被困离子逸出而有利于更紧密的结合。该模型对数据拟合良好,这与Armstrong和Cota所提出的Ca2+在削弱TTX结合方面比Na+更有效以及结合的Ca2+稳定通道的关闭状态一致。对反对被困离子机制的报告进行了批判性讨论。

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