首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Involvement of local anesthetic binding sites on IVS6 of sodium channels in fast and slow inactivation.
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Involvement of local anesthetic binding sites on IVS6 of sodium channels in fast and slow inactivation.

机译:钠通道IVS6上的局部麻醉剂结合位点参与快速和缓慢失活。

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摘要

Local anesthetics (LAs) block Na(+) channels with a higher affinity for the fast or slow inactivated state of the channel. Their binding to the channel may stabilize fast inactivation or induce slow inactivation. We examined the role of the LA binding sites on domain IV, S6 (IVS6) of Na(+) channels in fast and slow inactivation by studying the gating properties of the mutants on IVS6 affecting LA binding. Mutation of the putative LA binding site, F1579C, inhibited fast and slow inactivation. Mutations of another putative LA binding site, Y1586C, and IVS6 residue involved in LA access and binding, I1575C, both enhanced fast and slow inactivation. None of the mutations affected channel activation. These results suggest that the LA binding site on IVS6 is involved in slow inactivation as well as fast inactivation, and these two gatings are coupled at the binding site.
机译:局部麻醉药(LAs)阻止Na(+)通道对通道的快速或慢速灭活状态具有更高的亲和力。它们与通道的结合可稳定快速灭活或诱导缓慢灭活。我们通过研究影响LA结合的IVS6突变体的门控特性,研究了Na(+)通道的IV,S6(IVS6)域IV上LA结合位点的作用。推定的LA结合位点F1579C的突变抑制了快慢失活。参与LA访问和结合的另一个推定的LA结合位点Y1586C和IVS6残基I1575C的突变均增强了快速和慢速失活。这些突变均不影响通道激活。这些结果表明,IVS6上的LA结合位点参与了缓慢的失活以及快速的失活,并且这两个门控在结合位点偶联。

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