Membrane Hormone Receptors and Their Signaling Pathways as Targets for Endocrine Disruptors

被引:3
作者
Combarnous, Yves [1 ]
Thi Mong Diep Nguyen [1 ,2 ]
机构
[1] Tours Univ Joint Unit, Physiol Reprod & Comportements, CNRS, INRAe, F-37380 Nouzilly, France
[2] Quy Nhon Univ, Fac Nat Sci, Quy Nhon 820000, Vietnam
关键词
tyrosine kinase receptor; serine; threonine kinase receptor; cytokine receptor; G protein-coupled receptor; guanyl cyclase receptor; ion-channel receptor; orthosteric site; allosteric site; estradiol; bisphenols; WHO-UNEP-STATE; NATRIURETIC-PEPTIDE; ION CHANNELS; BISPHENOL-A; SCIENCE; ACTIVATION; CHEMICALS; PRESSURE; SITES;
D O I
10.3390/jox12020007
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The endocrine disruptors are mostly small organic molecules developed for numerous and very diverse industrial applications. They essentially act through nuclear receptors with small and hydrophobic endogenous ligands. Nevertheless, potential adverse effects through membrane hormone receptors cannot be ruled out, and have indeed been observed. The present paper reviews how orthosteric and allosteric binding sites of the different families of membrane receptors can be targets for man-made hydrophobic molecules (components of plastics, paints, flame retardants, herbicides, pesticides, etc.). We also review potential target proteins for such small hydrophobic molecules downstream of membrane receptors at the level of their intracellular signaling pathways. From the currently available information, although endocrine disruptors primarily affect nuclear receptors' signaling, membrane receptors for hormones, cytokines, neuro-mediators, and growth factors can be affected as well and deserve attention.
引用
收藏
页码:64 / 73
页数:10
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