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

机译:巨大克隆大鼠垂体前叶细胞的Erg内向整流K +电流及其促甲状腺激素释放激素的调节

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摘要

class="enumerated" style="list-style-type:decimal">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.IK,IR was isolated by the use of the selective erg (ether-à-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.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.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.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:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 利用生理学上的K + 生理梯度溶液研究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)。 IK,IR通过使用选择性erg(与醚相关的基因)通道阻滞剂E-4031分离。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,最大电流幅值为-40 mV。当K + 平衡电位EK变为负值时,发生大的瞬时内向电流。 IK的选择性药理学阻滞,当Ca 时IR引起膜电位持续去极化。 > 2 + 动作电位被阻断,证实了IK,IR对GH3 / B6细胞静止膜电位的贡献。 促甲状腺激素释放激素(TRH)有效降低了持续的向外和向内生长。瞬态向内IK,IR。 TRH引起的膜电位去极化的幅度与IK,IR的几乎完全降低是一致的。 结果表明TRH引起的IK,IR的减少能够介导静息电位去极化,表明在GH细胞TRH反应第二阶段期间发生的动作电位频率增加应通过IK,IR抑制来维持。而且,这是配体诱导的erg介导电流的生理调节的第一个证据。

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