探地雷达
雌激素
血管舒张
雌激素受体
内分泌学
内科学
血压
受体
一氧化氮
药理学
医学
化学
乳腺癌
癌症
作者
Matthias R. Meyer,Eric R. Prossnitz,Matthias Barton
出处
期刊:Immunology, endocrine and metabolic agents in medicinal chemistry
[Bentham Science]
日期:2011-12-01
卷期号:11 (4): 255-261
被引量:29
标识
DOI:10.2174/1871522211108040255
摘要
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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