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dc.rights.licenseopenen_US
dc.contributor.authorLY, Tu-Ky
dc.contributor.authorCHADILI, Edith
dc.contributor.authorPALLUEL, Olivier
hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorLE MENACH, Karyn
IDREF: 256879966
hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorBUDZINSKI, Hélène
ORCID: 0000-0003-1028-9154
IDREF: 070478090
dc.contributor.authorTEBBY, Cleo
dc.contributor.authorHINFRAY, Nathalie
dc.contributor.authorBEAUDOUIN, Rémy
dc.date.accessioned2025-04-16T07:45:01Z
dc.date.available2025-04-16T07:45:01Z
dc.date.issued2025-06
dc.identifier.issn0166-445Xen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/206219
dc.description.abstractEnEndocrine disruptors (EDs) can disrupt the gonadotropic axis, which consists of the Hypothalamus-Pituitary-Gonads (HPG), notably by altering aromatase (cyp19a), a key enzyme regulating the endocrine system and reproductive function in fish. The effects of EDs can be predicted by integrating both toxicokinetic (TK) and toxicodynamic (TD) processes in order to relate adverse outcomes to external exposures. In this study, we developed a physiologically based kinetic-toxicodynamic model to simulate the disruption of the HPG axis (PBK-TD, hereafter named PBK-HPG) in female zebrafish exposed to either of two aromatase inhibitors, imazalil or prochloraz. The model was calibrated using Bayesian methods and supported by novel experimental data, including measurements of vitellogenin, 17β-estradiol, and 11-ketotestosterone levels, along with in vivo monitoring of the cyp19a1a gene in transgenic cyp19a1a-GFP ebrafish. Seamless integration of a PBK model within a TD model of the HPG-axis, provided the link between external exposure and internal levels of imazalil and prochloraz in key organs, allowing for mechanistic predictions of their inhibitory effects on gonadal aromatase. Our PBK-HPG model accurately predicted both baseline homeostasis and the effects of aromatase inhibition, with all endocrine endpoints including reproductive disruption, i.e., decreased egg production, falling within a twofold range of both experimental and literature data. Therefore, our PBK-HPG model could further support the development of a mechanistic qAOP with TK considerations. The model offers significant potential for improving environmental risk assessments of EDs and possibly other stressors across species.
dc.language.isoENen_US
dc.subject.enEndocrine Discruptors
dc.subject.enGonadotropic axis
dc.subject.enHPG axis
dc.subject.enPBK-TD
dc.subject.enQST
dc.subject.enTKTD
dc.subject.enZebrafish
dc.subject.enqAOP
dc.title.enPBK-TD modelling of the gonadotropic axis: Case study with two azole fungicides in female zebrafish
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.aquatox.2025.107337en_US
dc.subject.halSciences de l'environnementen_US
bordeaux.journalAquatic Toxicologyen_US
bordeaux.page107337en_US
bordeaux.volume283en_US
bordeaux.hal.laboratoriesEPOCen_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.teamLPTCen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcecrossref
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcecrossref
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Aquatic%20Toxicology&rft.date=2025-06&rft.volume=283&rft.spage=107337&rft.epage=107337&rft.eissn=0166-445X&rft.issn=0166-445X&rft.au=LY,%20Tu-Ky&CHADILI,%20Edith&PALLUEL,%20Olivier&LE%20MENACH,%20Karyn&BUDZINSKI,%20H%C3%A9l%C3%A8ne&rft.genre=article


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