Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8950005 | Molecular and Cellular Endocrinology | 2018 | 39 Pages |
Abstract
Proper cyclicity is essential to reach successful optimal fertility. In rats and mice, BPA exposure is repeatedly and reliably reported to show an adverse effect on the estrous cycle after exposures at different life stages. In humans, a possible association between modifications of menstrual cycle characteristics (e.g. length of the cycle, duration of menstrual bleeding) and sub-fecundity or spontaneous abortion has been observed. Alterations of ovarian cyclicity can therefore be definitely considered as an adverse health outcome. As a prerequisite for the EU REACH regulation to identify a substance as an endocrine disruptor and a SVHC,1 the proof has to be established that the substance can have deleterious health effects resulting from an endocrine mode of action. This review provides an overview of the currently available data allowing to conclude that the adverse effects of BPA exposure on ovarian cyclicity is mediated by an endocrine mode of action.
Keywords
HPGWOEGPEREE2↓↑KISS1RproestrusMOAdehydroepiandrosteroneSVHCPPARγAVPVEuropean Chemical AgencyECHAOVXovariectomizedPRL3β-Hydroxysteroid dehydrogenasePGF2αGATA4BMP-15CREBDPCBPASF-1IGF-2US National Toxicology ProgramGDF-9DHEARACNTPAOPGnRHPCNALRH1PCOSPPTPNDRT-PCRPII17-β estradiolG protein-coupled estrogen receptorProliferating Cell Nuclear AntigenEuropean UnionEthinylestradiolcorpora luteaEndocrine disruptionDESestradiol benzoateEstrogenSprague DawleyIncreaseBisphenol AtestosteroneFemale reproductionRegistration, Evaluation, Authorisation and Restriction of ChemicalsMode of actionANSESDiethylstilbestrolREACHgestation daypostnatal daydays post conceptionFemaleWorld Health OrganizationStarPolycystic ovary syndromeinsulin-like growth factor 2ArcIn vitro fertilizationIVFHypothalamic–pituitary–gonadal axisendocrine disruptoradverse outcome pathwayMaledecreasearcuate nucleusanteroventral periventricular nucleusgonadotrophin-releasing hormonefollicle stimulating hormoneluteinizing hormoneFSHreverse transcription polymerase chain reactionbody weightWeight of evidencesteroid acute regulatory proteincAMP response element-binding proteinProlactinWHOEstrogen receptorProgesterone receptorliver receptor homolog 1Kisspeptin receptorPeroxisome proliferator activated receptor gamma
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Authors
Catherine Viguié, Sakina Mhaouty-Kodja, René Habert, Cécile Chevrier, Cécile Michel, Elodie Pasquier,