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Role of phosphodiesterases in modulation of BKCa channels in hypertensive pulmonary arterial smooth muscle

机译:磷酸二酯酶在高血压肺动脉平滑肌BKCa通道调节中的作用

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摘要

BKCa channels regulate pulmonary arterial pressure, and protein kinase C (PKC) inhibits BKCa channels, but little is known about PKC-mediated modulation of BKCa channel activity in pulmonary arterial smooth muscle. Studies were done to determine mechanisms of PKC modulation of BKCa channel activity in pulmonary arterial smooth muscle cells (PASMC) of the Fawn-hooded rat (FHR), an animal model of pulmonary hypertension. Forskolin opened BKCa channels in FHR PASMC, which was blocked by PKC activation, and reversed by the phosphodiesterase (PDE) inhibitors IBMX, milrinone, and zaprinast. PDE inhibition also blocked the vasoconstrictor response to PKC activation in FHR pulmonary arteries. These results indicate that PKC inhibits cAMP-induced activation of BKCa channels and causes pulmonary vasoconstriction in hypertensive pulmonary arterial smooth muscle via PDE, which further suggests PDE inhibitors for treatment of pulmonary hypertension.
机译:BKCa通道调节肺动脉压,蛋白激酶C(PKC)抑制BKCa通道,但是关于PKC介导的BKCa通道在肺动脉平滑肌中的活性调节知之甚少。进行了研究以确定PKH调节肺动脉高压动物模型“ Fawn-hooded rat”(FHR)的肺动脉平滑肌细胞(PASMC)中BKCa通道活性的机制。福斯高林在FHR PASMC中打开了BKCa通道,该通道被PKC激活所阻断,并被磷酸二酯酶(PDE)抑制剂IBMX,米力农和扎普利纳特逆转。 PDE抑制还阻断了FHR肺动脉中对PKC激活的血管收缩反应。这些结果表明PKC通过PDE抑制了cAMP诱导的BKCa通道的激活并引起了高血压肺动脉平滑肌的肺血管收缩,这进一步提示了PDE抑制剂可用于治疗肺动脉高压。

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