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2,4-dichlorophenoxyacetic acid (2,4-D) exposure during postnatal development alters the effects of western diet on mouse prostate

dc.contributor.authorRocha, V. A. [UNESP]
dc.contributor.authorAquino, A. M. [UNESP]
dc.contributor.authorMagosso, N. [UNESP]
dc.contributor.authorSouza, P. V. [UNESP]
dc.contributor.authorJustulin, L. A. [UNESP]
dc.contributor.authorDomeniconi, R. F. [UNESP]
dc.contributor.authorBarbisan, L. F. [UNESP]
dc.contributor.authorRomualdo, G. R. [UNESP]
dc.contributor.authorScarano, W. R. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:59:18Z
dc.date.issued2023-09-01
dc.description.abstractWestern diet (WD), abundant in saturated fats and simple carbohydrates, has been associated with the development of prostate diseases. In addition, 2,4-dichlorophenoxyacetic acid (2,4-D), an herbicide used in agricultural and non-agricultural settings, may interfere with the endocrine system impacting reproductive health. The association of both factors is something common in everyday life, however, there are no relevant studies associating them as possible modulators of prostatic diseases. This study evaluated the action of the herbicide 2,4-D on the postnatal development of the prostate in mice fed with WD. Male C57Bl/6J mice received simultaneously a WD and 2,4-D at doses of 0.02, 2.0, or 20.0 mg/kg b.w./day for 6 months. The prolongated WD intake induced obesity and glucose intolerance, increasing body weight and fat. WD induced morphological changes and increased PCNA-positive epithelial cells in prostate. Additionally, the WD increased gene expression of AR, antioxidant targets, inflammation-related cytokines, cell repair and turnover, and targets related to methylation and miRNAs biosynthesis compared to the counterpart (basal diet). 2,4-D (0.02 and 2.0) changed prostate morphology and gene expression evoked by WD. In contrast, the WD group exposed to 20 mg/kg of 2,4-D reduced feed intake and body weight, and increased expression of androgen receptor and genes related to cell repair and DNA methylation compared to the negative control. Our results showed that 2,4-D was able to modulate the effects caused by WD, mainly at lower doses. However, further studies are needed to elucidate the mechanisms of 2,4-D on the obesogenic environment caused by the WD.en
dc.description.affiliationSão Paulo State University (UNESP) Department of Structural and Functional Biology Institute of Biosciences, São Paulo
dc.description.affiliationSão Paulo State University (UNESP) Botucatu Medical School Experimental Research Unit (UNIPEX) Multimodel Drug Screening Platform – Laboratory of Chemically induced and Experimental Carcinogenesis (MDSP-LCQE), SP
dc.description.affiliationUnespSão Paulo State University (UNESP) Department of Structural and Functional Biology Institute of Biosciences, São Paulo
dc.description.affiliationUnespSão Paulo State University (UNESP) Botucatu Medical School Experimental Research Unit (UNIPEX) Multimodel Drug Screening Platform – Laboratory of Chemically induced and Experimental Carcinogenesis (MDSP-LCQE), SP
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdCAPES: 001
dc.description.sponsorshipIdCNPq: 312028/2022–9 -WRS
dc.identifierhttp://dx.doi.org/10.1016/j.reprotox.2023.108449
dc.identifier.citationReproductive Toxicology, v. 120.
dc.identifier.doi10.1016/j.reprotox.2023.108449
dc.identifier.issn1873-1708
dc.identifier.issn0890-6238
dc.identifier.scopus2-s2.0-85168809378
dc.identifier.urihttps://hdl.handle.net/11449/301752
dc.language.isoeng
dc.relation.ispartofReproductive Toxicology
dc.sourceScopus
dc.subject2
dc.subject4-D
dc.subjectHerbicides
dc.subjectObesity
dc.subjectProstate
dc.subjectReproductive toxicology
dc.title2,4-dichlorophenoxyacetic acid (2,4-D) exposure during postnatal development alters the effects of western diet on mouse prostateen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt

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