GPER/GPR30与血管张力和血压的调节。

Matthias R Meyer, Eric R Prossnitz, Matthias Barton
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引用次数: 27

摘要

天然雌激素如17β-雌二醇是内源性血管扩张剂,与高血压的性别差异有关。这些激素激活雌激素受体ERα和ERβ,介导部分雌激素依赖性血管舒张。此外,一种名为GPER/GPR30的新型G蛋白偶联雌激素结合受体已被发现在心血管系统中表达。通过敲除动物或选择性靶向GPER/GPR30的药物,该受体作为涉及一氧化氮(NO)和降血压活性的急性雌激素依赖性血管舒张的介质的重要作用已被证明。越来越多的证据表明GPER/GPR30负责控制血管张力,这表明该受体可能是绝经后女性和男性高血压药物治疗的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GPER/GPR30 and Regulation of Vascular Tone and Blood Pressure.

Natural estrogens such as 17β-estradiol are endogenous vasodilators and have been implicated in the gender differences of hypertension. These hormones activate estrogen receptors ERα and ERβ, which mediate part of estrogen-dependent vasodilation. In addition, a novel G protein-coupled estrogen-binding receptor termed GPER/GPR30 has been identified that is expressed in the cardiovascular system. Using knock-out animals or drugs selectively targeting GPER/GPR30, a significant role for this receptor as a mediator of acute estrogen-dependent vasodilation involving nitric oxide (NO) and blood pressure-lowering activity has been demonstrated. The accumulating evidence that GPER/GPR30 is responsible for control of vascular tone indicates that this receptor may represent a novel drug target for pharmacologic treatment of hypertension in postmenopausal women and possibly also men.

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