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Mechanisms of methyclothiazide-induced inhibition of contractile responses in rat aorta.

机译:甲乙噻嗪诱导的大鼠主动脉收缩反应抑制机制。

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摘要

Methyclothiazide (MCTZ), a thiazide diuretic, inhibits the contractile response induced by norepinephrine in aortic rings from 12-week-old spontaneously hypertensive rats (SHR). Although not modified by indomethacin, this inhibition was attenuated by either mechanical removal of the endothelium or N omega-nitro-L-arginine (NOLA) treatment. These results suggest that the MCTZ effects on the norepinephrine-evoked vascular response are mediated by an endothelium-dependent mechanism involving endothelium-dependent relaxing factor (EDRF)itric oxide (NO) release. MCTZ was also found to alter the contractile response induced by the addition of Ca(2+) to a depolarizing solution, and this inhibitory effect was partially abolished by NOLA application. Our data led us to propose that MCTZ relaxes aortic rings, resulting in an endothelium-dependent relaxation phenomenon that could even be reinforced under high-K(+) depolarizing conditions.
机译:噻嗪类利尿剂甲乙噻嗪(MCTZ)抑制了12周龄自发性高血压大鼠(SHR)在主动脉环中由去甲肾上腺素引起的收缩反应。尽管没有被吲哚美辛修饰,但是通过机械去除内皮或N-ω-硝基-L-精氨酸(NOLA)处理减弱了这种抑制作用。这些结果表明,MCTZ对去甲肾上腺素诱发的血管反应的影响是由内皮依赖性机制介导的,该机制涉及内皮依赖性松弛因子(EDRF)/一氧化氮(NO)释放。还发现MCTZ改变了通过在去极化溶液中添加Ca(2+)诱导的收缩反应,而NOLA的应用部分消除了这种抑制作用。我们的数据使我们提出MCTZ松弛主动脉环,导致内皮依赖性松弛现象,甚至在高K(+)去极化条件下也可以增强。

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