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Potassium current inhibition by nonselective cation channel-mediated sodium entry in rat pheochromocytoma (PC-12) cells.

机译:非选择性阳离子通道介导的钠进入大鼠嗜铬细胞瘤(PC-12)细胞的钾电流抑制作用。

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摘要

Under physiological conditions, nonselective cation (NSC) channels mediate the entry of cations into cells, the most important being Na+ and Ca2+. In contrast to the Ca(2+)-dependent signaling mechanisms, little is known about the consequences and the spatial distribution of intracellular [Na+] elevation. In this study we demonstrate that Na+ entry, during the opening of ATP-activated NSC channels, leads to an inhibition of voltage-dependent K+ currents (IK) in cromaffin-like undifferentiated PC-12 cells. The effect was dependent on the charge carrier as well as on the density of the ATP-activated current. Extracellular alkali cations (Na+, Li+) were more efficient than NH4+ in suppressing IK. Intracellular infusion of Na+ had the same effect as Na+ influx through ATP-activated NSC channels. The inhibition of IK persisted when the total ATP-induced Na+ entry was reduced by membrane depolarization, suggesting a spatial restriction of the required Na+ accumulation. Our results indicate that NSC channels influence the function of other ion channels by changing local intracellular ion concentrations.
机译:在生理条件下,非选择性阳离子(NSC)通道介导阳离子进入细胞,最重要的是Na +和Ca2 +。与依赖Ca(2+)的信号传导机制相反,关于细胞内[Na +]升高的后果和空间分布知之甚少。在这项研究中,我们证明,在ATP激活的NSC通道开放期间,Na +进入会导致抑制像铬烷一样的未分化PC-12细胞中的电压依赖性K +电流(IK)。效果取决于载流子以及ATP激活电流的密度。在抑制IK方面,细胞外碱性阳离子(Na +,Li +)比NH4 +更有效。细胞内注入Na +与通过ATP激活的NSC通道流入Na +具有相同的作用。当总ATP诱导的Na +进入通过膜去极化减少时,IK的抑制作用持续存在,表明所需Na +积累的空间限制。我们的结果表明,NSC通道通过改变局部细胞内离子浓度来影响其他离子通道的功能。

著录项

  • 作者

    Strübing, C; Hescheler, J;

  • 作者单位
  • 年度 1996
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  • 原文格式 PDF
  • 正文语种 en
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