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GPER 作为内分泌干扰物 (EDCs) 的受体。

GPER as a Receptor for Endocrine-Disrupting Chemicals (EDCs).

机构信息

Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, Université Lyon 1, CNRS UMR5242, Ecole Normale Supérieure de Lyon, Lyon, France.

出版信息

Front Endocrinol (Lausanne). 2020 Aug 19;11:545. doi: 10.3389/fendo.2020.00545. eCollection 2020.

Abstract

Endocrine-disrupting chemicals (EDCs) are exogenous chemicals that interfere with endogenous hormonal systems at various levels, resulting in adverse health effects. EDCs belong to diverse chemical families and can accumulate in the environment, diet and body fluids, with different levels of persistence. Their action can be mediated by several receptors, including members of the nuclear receptor family, such as estrogen and androgen receptors. The G protein-coupled estrogen receptor (GPER), a seven-transmembrane domain receptor, has also attracted attention as a potential target of EDCs. This review summarizes our current knowledge concerning GPER as a mediator of EDCs' effects.

摘要

内分泌干扰化学物质(EDCs)是指在各种水平上干扰内源性激素系统的外源性化学物质,导致不良健康影响。EDCs 属于不同的化学家族,可在环境、饮食和体液中积累,具有不同程度的持久性。它们的作用可以通过几种受体介导,包括核受体家族的成员,如雌激素和雄激素受体。G 蛋白偶联雌激素受体(GPER),一种七跨膜域受体,也作为 EDCs 的潜在作用靶点而受到关注。本综述总结了我们目前关于 GPER 作为 EDCs 作用的中介物的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3e/7466721/ac784b5d4a21/fendo-11-00545-g0001.jpg

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