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首页> 外文期刊>Biochemical Pharmacology >Inhibitory action of ICI-182,780, an estrogen receptor antagonist, on BK(Ca) channel activity in cultured endothelial cells of human coronary artery.
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Inhibitory action of ICI-182,780, an estrogen receptor antagonist, on BK(Ca) channel activity in cultured endothelial cells of human coronary artery.

机译:ICI-182,780(一种雌激素受体拮抗剂)对人冠状动脉内皮细胞中BK(Ca)通道活性的抑制作用。

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摘要

ICI-182,780 is known to be a selective inhibitor of the intracellular estrogen receptors. The effect of ICI-182,780 on ion currents was studied in cultured endothelial cells of human coronary artery. In whole-cell current recordings, ICI-182,780 reversibly decreased the amplitude of K(+) outward currents. The decrease in outward current caused by ICI-182,780 could be counteracted by further application of magnolol or nordihydroguaiaretic acid, yet not by 17beta-estradiol. Under current-clamp condition, ICI-182,780 (3microM) depolarized the membrane potentials of the cells, and magnolol (10microM) or nordihydroguaiaretic acid (10microM) reversed ICI-182,780-induced depolarization. In inside-out patches, ICI-182,780 added to the bath did not alter single-channel conductance of large-conductance Ca(2+)-activated K(+) channels (BK(Ca) channels), but decreased their open probability. ICI-182,780 reduced channel activity in a concentration-dependent manner with an IC(50) value of 3microM. After BK(Ca) channel activity was suppressed by 2-methoxyestradiol (3microM), subsequent application of ICI-182,780 (3microM) did not further reduce the channel activity. The application of ICI-182,780 shifted the activation curve of BK(Ca) channels to positive potentials. Its decrease in the open probability primarily involved a reduction in channel open duration. ICI-182,780 also suppressed the proliferation of these endothelial cells with an IC(50) value of 2microM. However, in coronary smooth muscle cells, a bell-shaped concentration-response curve for the ICI-182,780 effect on BK(Ca) channel activity was observed. This study provides evidence that ICI-182,780 can inhibit BK(Ca) channels in vascular endothelial cells in a mechanism unlikely to be linked to its anti-estrogen activity. The inhibitory effects on these channels may partly contribute to the underlying mechanisms by which ICI-182,780 affects endothelial function.
机译:已知ICI-182,780是细胞内雌激素受体的选择性抑制剂。在培养的人冠状动脉内皮细胞中研究了ICI-182,780对离子电流的影响。在全细胞电流记录中,ICI-182,780可逆地降低了K(+)向外电流的幅度。由ICI-182,780引起的向外电流的减少可以通过进一步应用厚朴酚或降冰片氢愈创木酸来抵制,但不能通过17β-雌二醇来抵制。在电流钳制条件下,ICI-182,780(3microM)使细胞的膜电位去极化,厚朴酚(10microM)或去甲二氢愈创木酸(10microM)使ICI-182,780诱导的去极化逆转。在由内而外的修补程序中,添加到浴中的ICI-182,780不会更改大电导Ca(2+)激活的K(+)通道(BK(Ca)通道)的单通道电导,但会降低其打开概率。 ICI-182,780以浓度依赖性方式降低了通道活性,IC(50)值为3microM。在BK(Ca)通道活性被2-甲氧基雌二醇(3microM)抑制后,随后应用ICI-182,780(3microM)并没有进一步降低通道活性。 ICI-182,780的应用将BK(Ca)通道的激活曲线移至正电位。其开放概率的减少主要涉及信道开放持续时间的减少。 ICI-182,780还以2microM的IC(50)值抑制了这些内皮细胞的增殖。但是,在冠状动脉平滑肌细胞中,观察到了ICI-182,780对BK(Ca)通道活性的钟形浓度-响应曲线。这项研究提供的证据表明,ICI-182,780可以抑制血管内皮细胞中的BK(Ca)通道,其机制可能与其抗雌激素活性无关。对这些通道的抑制作用可能部分促成ICI-182,780影响内皮功能的潜在机制。

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