G-Protein Coupled Hormone Receptors of the Hypothalamic-Pituitary-Gonadal Axis are Targets of Endocrine Disrupting Chemicals

V. Suteau, P. Rodien, M. Munier
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Abstract

Endocrine-disrupting chemicals have received significant concern, since they ubiquitously persist in the environment and are able to induce adverse effects on health, and more particularly on reproductive function. Most of the studies focused on nuclear hormone receptors as mediators of sex steroid hormones signaling. However, there are increasing evidences that peptides hormones of the Hypothalamo-Pituitary-Gonadal axis are targets of endocrine-disrupting chemicals (as Gonadotropin-Releasing Hormone, Follicle-Stimulating Hormone, Luteinizing Hormone…). The majority of these hormones act on G protein-coupled membrane receptors. This review summarizes the effects of endocrine-disrupting chemicals on homeostasis of peptides hormone of Hypothalamo-Pituitary-Gonadal axis and on their G protein-coupled membrane receptors signaling revealed by experimental, clinical, and epidemiological studies in human.
下丘脑-垂体-性腺轴的g蛋白偶联激素受体是内分泌干扰物的靶点
干扰内分泌的化学物质受到了极大的关注,因为它们在环境中无处不在地持续存在,能够对健康,特别是对生殖功能产生不利影响。大多数研究集中在核激素受体作为性类固醇激素信号的介质上。然而,越来越多的证据表明,下丘脑-垂体-性腺轴的多肽激素是内分泌干扰物质(如促性腺激素释放激素、促卵泡激素、促黄体生成素等)的靶标。这些激素大多作用于G蛋白偶联膜受体。本文综述了内分泌干扰物对人体下丘脑-垂体-性腺轴多肽激素稳态及对其G蛋白偶联膜受体信号传导的影响,并结合实验、临床和流行病学研究进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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