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Iptakalim, a novel ATP-sensitive potassium channel opener, inhibits pulmonary arterial smooth muscle cell proliferation by downregulation of PKC-α

机译:新型ATP敏感性钾通道开放剂Iptakalim通过下调PKC-α抑制肺动脉平滑肌细胞增殖

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摘要

Iptakalim is a new ATP-sensitive potassium (KATP) channel opener, and it inhibits the proliferation of pulmonary arterial smooth muscle cells (PASMCs) and pulmonary vascular remodeling. However, the underlying mechanism remains unclear. In the present study, we found that iptakalim significantly decreased pulmonary artery pressure, inhibited pulmonary ariery remodeling and PKC-α overexpression in chronic hypoxia in a rat pulmonary hypertension model. Iptakalim reduced hypoxia-induced expression of PKC-α, and abolished the effect of hypoxia on PASMC proliferation significantly in a dose-dependent manner in vitro. Moreover, these effects were abolished by glibenclamide, a selective KATP channel antagonist. These results indicate that iptakalim inhibits PASMC proliferation and pulmonary vascular remodeling induced by hypoxia through downregulating the expression of PKC-α. Iptakalim can serve as a novel promising treatment for hypoxic pulmonary hypertension.
机译:依他卡林是一种新型的ATP敏感性钾(KATP)通道开放剂,它抑制肺动脉平滑肌细胞(PASMC)的增殖和肺血管重构。但是,其潜在机制仍不清楚。在本研究中,我们发现在大鼠肺动脉高压模型中,依他卡林可显着降低肺动脉压力,抑制肺动脉重构和PKC-α过表达。依他卡林在体外以剂量依赖的方式降低了低氧诱导的PKC-α表达,并消除了低氧对PASMC增殖的影响。而且,选择性KATP通道拮抗剂格列本脲消除了这些作用。这些结果表明,伊他卡林通过下调PKC-α的表达来抑制缺氧引起的PASMC增殖和肺血管重构。依他卡林可以作为一种治疗缺氧性肺动脉高压的新方法。

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