Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hubei Key Laboratory of Biological Targeted Therapy, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Front Endocrinol (Lausanne). 2023 Aug 17;14:1226458. doi: 10.3389/fendo.2023.1226458. eCollection 2023.
Aldosterone is one of the most essential hormones synthesized by the adrenal gland because it regulates water and electrolyte balance. G protein-coupled estrogen receptor (GPER) is a newly discovered aldosterone receptor, which is proposed to mediate the non-genomic pathways of aldosterone while the hormone simultaneously interacts with mineralocorticoid receptor. In contrast to its cardio-protective role in postmenopausal women via its interaction with estrogen, GPER seems to trigger vasoconstriction effects and can further induce water and sodium retention in the presence of aldosterone, indicating two entirely different binding sites and effects for estrogen and aldosterone. Accumulating evidence also points to a role of aldosterone in mediating hypertension and its risk factors via the interaction with GPER. Therefore, with this review, we aimed to summarize the research on these interactions to help (1) elucidate the role of GPER activated by aldosterone in the blood vessels, heart, and kidney; (2) compare the non-genomic actions between aldosterone and estrogen mediated by GPER; and (3) address the potential of GPER as a new promising therapeutic target for aldosterone-induced hypertension.
醛固酮是肾上腺合成的最重要的激素之一,因为它调节水和电解质平衡。G 蛋白偶联雌激素受体(GPER)是一种新发现的醛固酮受体,它被提议介导醛固酮的非基因组途径,而激素同时与盐皮质激素受体相互作用。与它在绝经后妇女中通过与雌激素相互作用的心脏保护作用相反,GPER 似乎会引发血管收缩作用,并在醛固酮存在的情况下进一步导致水和钠的潴留,表明雌激素和醛固酮具有两个完全不同的结合位点和作用。越来越多的证据也表明,醛固酮通过与 GPER 的相互作用在介导高血压及其危险因素方面发挥作用。因此,通过本文的综述,我们旨在总结这些相互作用的研究,以帮助阐明:(1)醛固酮激活的 GPER 在血管、心脏和肾脏中的作用;(2)由 GPER 介导的醛固酮和雌激素之间的非基因组作用;以及(3)GPER 作为醛固酮诱导的高血压新的有前途的治疗靶点的潜力。