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Effects of bisphenol A alternatives (BPS and BPAF) on zebrafish (Danio rerio) spermatogenesis ex vivo: meiosis damage and transcriptional deregulation of genes related to spermatogenic processes and epigenetic regulation

dc.contributor.authorCosta, Daniel Fernandes da [UNESP]
dc.contributor.authorRodrigues, Maira da Silva [UNESP]
dc.contributor.authorBorali, Luciana Marino [UNESP]
dc.contributor.authorSouza, Beatriz Marques de [UNESP]
dc.contributor.authorHabibi, Hamid R
dc.contributor.authorNóbrega, Rafael Henrique [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)pt
dc.date.accessioned2026-07-22T19:54:55Z
dc.date.issued2025-07-10
dc.description.abstractEnvironmental contaminants BPS and BPAF, emerging substitutes for BPA, are raising concerns as endocrine disruptors. This study assessed their effects on zebrafish spermatogenesis using ex vivo testicular explants exposed to 0.5, 5, or 50 µg/L of each compound for 7 days. Both chemicals impaired spermatogenesis by reducing meiotic (Spc<sub>p</sub>) and post-meiotic (Spt) cyst formation, with BPS showing stronger effects. Additionally, they altered the expression of marker genes related to spermatogenesis, steroidogenesis, and epigenetic regulation. Notably, cyp19a1a was upregulated by both, indicating estrogenic activity; however, BPS did not affect estrogen receptor expression, suggesting an indirect antiandrogenic mechanism, while BPAF modulated esr1 and esr2a, indicating direct estrogenic effects. Our findings provide evidence that the dose-response for both compounds was non-monotonic. These results imply that BPS and BPAF can disrupt reproductive and molecular processes, challenging their safety as BPA substitutes and highlighting the need for further investigation and more stringent environmental regulations.
dc.description.affiliationReproductive and Molecular Biology Group, Department of Structural and Functional Biology, Institute of Biosciences, São Paulo State University (UNESP), Botucatu, São Paulo 18618-970, Brazil.
dc.description.affiliationDepartment of Biological Sciences, University of Calgary, Calgary, AB 2500, Canada.
dc.description.affiliationReproductive and Molecular Biology Group, Department of Structural and Functional Biology, Institute of Biosciences, São Paulo State University (UNESP), Botucatu, São Paulo 18618-970, Brazil. Electronic address: rafael.nobrega@unesp.br.
dc.description.affiliationUnespReproductive and Molecular Biology Group, Department of Structural and Functional Biology, Institute of Biosciences, São Paulo State University (UNESP), Botucatu, São Paulo 18618-970, Brazil.
dc.description.affiliationUnespReproductive and Molecular Biology Group, Department of Structural and Functional Biology, Institute of Biosciences, São Paulo State University (UNESP), Botucatu, São Paulo 18618-970, Brazil. Electronic address: rafael.nobrega@unesp.br.
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1190685145
dc.identifier.dimensionspub.1190685145
dc.identifier.doi10.1016/j.etap.2025.104757
dc.identifier.issn1382-6689
dc.identifier.issn1872-7077
dc.identifier.orcid0000-0001-5236-2861
dc.identifier.orcid0000-0002-4368-6853
dc.identifier.orcid0000-0001-9796-5076
dc.identifier.pmid40651513
dc.identifier.urihttps://hdl.handle.net/11449/328430
dc.publisherElsevier
dc.relation.ispartofEnvironmental Toxicology and Pharmacology; v. 117; p. 104757
dc.rights.accessRightsAcesso restritopt
dc.rights.sourceRightsclosed
dc.sourceDimensions
dc.titleEffects of bisphenol A alternatives (BPS and BPAF) on zebrafish (Danio rerio) spermatogenesis ex vivo: meiosis damage and transcriptional deregulation of genes related to spermatogenic processes and epigenetic regulation
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt

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