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

Inhibitory action of ICI-182,780, an estrogen receptor antagonist, on BK(Ca) channel activity in cultured endothelial cells of human coronary artery.

作者信息

Liu Yen-Chin, Lo Yi-Ching, Huang Chin-Wei, Wu Sheng-Nan

机构信息

Department of Anesthesiology, Kaohsiung Veterans General Hospital, City, ROC, Kaohsiung, Taiwan.

出版信息

Biochem Pharmacol. 2003 Nov 15;66(10):2053-63. doi: 10.1016/s0006-2952(03)00584-7.

Abstract

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 (10 microM) or nordihydroguaiaretic acid (10 microM) 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 3 microM. After BK(Ca) channel activity was suppressed by 2-methoxyestradiol (3 microM), subsequent application of ICI-182,780 (3 microM) 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 2 microM. 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.

摘要

众所周知,ICI-182,780是细胞内雌激素受体的选择性抑制剂。研究了ICI-182,780对人冠状动脉培养内皮细胞离子电流的影响。在全细胞电流记录中,ICI-182,780可逆地降低K(+)外向电流的幅度。ICI-182,780引起的外向电流降低可被进一步应用厚朴酚或去甲二氢愈创木酸抵消,但不能被17β-雌二醇抵消。在电流钳制条件下,ICI-182,780(3μM)使细胞的膜电位去极化,厚朴酚(10μM)或去甲二氢愈创木酸(10μM)逆转ICI-182,780诱导的去极化。在膜内面向外的膜片上,添加到浴中的ICI-182,780不会改变大电导Ca(2+)激活K(+)通道(BK(Ca)通道)的单通道电导,但会降低其开放概率。ICI-182,780以浓度依赖性方式降低通道活性,IC(50)值为3μM。在用2-甲氧基雌二醇(3μM)抑制BK(Ca)通道活性后,随后应用ICI-182,780(3μM)不会进一步降低通道活性。ICI-182,780的应用使BK(Ca)通道的激活曲线向正电位移动。其开放概率的降低主要涉及通道开放持续时间的缩短。ICI-182,780还以IC(50)值为2μM抑制这些内皮细胞的增殖。然而,在冠状动脉平滑肌细胞中,观察到ICI-182,780对BK(Ca)通道活性的浓度-反应曲线呈钟形。本研究提供了证据,表明ICI-182,780可以通过一种不太可能与其抗雌激素活性相关的机制抑制血管内皮细胞中的BK(Ca)通道。对这些通道的抑制作用可能部分有助于ICI-182,780影响内皮功能的潜在机制。

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