...
首页> 外文期刊>The Journal of Physiology >The erg inwardly rectifying K+ current and its modulation by thyrotrophin-releasing hormone in giant clonal rat anterior pituitary cells.
【24h】

The erg inwardly rectifying K+ current and its modulation by thyrotrophin-releasing hormone in giant clonal rat anterior pituitary cells.

机译:巨大的克隆大鼠垂体前叶细胞中的erg内向整流K +电流及其受促甲状腺激素释放激素的调节。

获取原文
获取原文并翻译 | 示例
           

摘要

1. The voltage-dependent inwardly rectifying K+ current (IK,IR) of clonal rat anterior pituitary cells (GH3/B6) was investigated in solutions with physiological K+ gradient using giant polynuclear cells. 2. IK,IR was isolated by the use of the selective erg (ether-a-go-go-related gene) channel blocker E-4031. In external 5 mM K+ solution, IK,IR carried steady-state outward current in the potential range between -60 and 0 mV, with a maximum current amplitude at -40 mV. Negative to the K+ equilibrium potential, EK, large transient inward currents occurred. 3. A selective pharmacological block of IK,IR induced a sustained depolarization of the membrane potential when Ca2+ action potentials were blocked, confirming the contribution of IK,IR to the resting membrane potential of GH3/B6 cells. 4. Thyrotrophin-releasing hormone (TRH) reduced effectively the sustained outward and the transient inward IK,IR. The magnitude of a TRH-induced depolarization of the membrane potential was consistent with an almost complete reduction of IK,IR. 5. The results demonstrate that the TRH-induced reduction of IK,IR is able to mediate the resting potential depolarization, suggesting that the increase in the frequency of action potentials occurring during the second phase of the TRH response in GH cells should be sustained by IK,IR inhibition. Moreover, this is the first evidence of a ligand-induced physiological modulation of an erg-mediated current.
机译:1.用巨型多核细胞在具有生理性K +梯度的溶液中研究了克隆的大鼠垂体前叶细胞(GH3 / B6)的电压依赖性向内整流K +电流(IK,IR)。 2.通过使用选择性erg(与醚相关的基因)通道阻断剂E-4031分离IK,IR。在外部5 mM K +解决方案中,IK,IR携带的稳态向外电流处于-60至0 mV的电势范围内,最大电流幅度为-40 mV。相对于K +平衡电位EK而言,出现了较大的瞬态内向电流。 3.当阻断Ca 2+动作电位时,IK,IR的选择性药理学阻断作用引起膜电位的持续去极化,证实了IK,IR对GH3 / B6细胞静息膜电位的贡献。 4.促甲状腺激素释放激素(TRH)有效降低了持续向外和短暂向内的IK,IR。 TRH诱导的膜电位去极化的幅度与IK,IR几乎完全降低是一致的。 5.结果表明TRH诱导的IK,IR降低能够介导静息电位去极化,这表明GH细胞在TRH反应第二阶段期间发生的动作电位频率的增加应通过IK,IR抑制。而且,这是erg介导的电流的配体诱导的生理调节的第一个证据。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号