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Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming

dc.contributor.authorBorges, Cibele S. [UNESP]
dc.contributor.authorDias, Ana Flávia M.G. [UNESP]
dc.contributor.authorRosa, Josiane Lima [UNESP]
dc.contributor.authorSilva, Patricia V. [UNESP]
dc.contributor.authorSilva, Raquel F. [UNESP]
dc.contributor.authorBarros, Aline L. [UNESP]
dc.contributor.authorSanabria, Marciana [UNESP]
dc.contributor.authorGuerra, Marina T. [UNESP]
dc.contributor.authorGregory, Mary
dc.contributor.authorCyr, Daniel G.
dc.contributor.authorDe G. Kempinas, Wilma [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversity of Quebec
dc.date.accessioned2018-12-11T17:03:39Z
dc.date.available2018-12-11T17:03:39Z
dc.date.issued2016-08-01
dc.description.abstractAntenatal betamethasone is used for accelerating fetal lung maturation for women at risk of preterm birth. Altered sperm parameters were reported in adult rats after intrauterine exposure to betamethasone. In this study, male rat offspring were assessed for reproductive development after dam exposure to betamethasone (0.1 mg/kg) or vehicle on Days 12, 13, 18 and 19 of pregnancy. The treatment resulted in reduction in the offspring body weight, delay in preputial separation, decreased seminal vesicle weight, testosterone levels and fertility, and increased testicular weight. In the testis, morphologically abnormal seminiferous tubules were observed, characterized by an irregular cell distribution with Sertoli cell that were displaced towards the tubular lumen. These cells expressed both Connexin 43 (Cx43) and Proliferative Nuclear Cell Antigen (PCNA). In conclusion, intrauterine betamethasone treatment appears to promote reproductive programming and impairment of rat sexual development and fertility due to, at least in part, unusual testicular disorders.en
dc.description.affiliationDepartment of Morphology Institute of Biosciences Univ Estadual Paulista-UNESP, Distrito de Rubião Junior s/n
dc.description.affiliationLaboratory for Reproductive Toxicology INRS-Institut Armand-Frappier University of Quebec, 531 boulevard des Prairies
dc.description.affiliationUnespDepartment of Morphology Institute of Biosciences Univ Estadual Paulista-UNESP, Distrito de Rubião Junior s/n
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdCNPq: 308842/2013-8
dc.format.extent125-134
dc.identifierhttp://dx.doi.org/10.1016/j.reprotox.2016.05.021
dc.identifier.citationReproductive Toxicology, v. 63, p. 125-134.
dc.identifier.doi10.1016/j.reprotox.2016.05.021
dc.identifier.file2-s2.0-84975295557.pdf
dc.identifier.issn1873-1708
dc.identifier.issn0890-6238
dc.identifier.scopus2-s2.0-84975295557
dc.identifier.urihttp://hdl.handle.net/11449/173105
dc.language.isoeng
dc.relation.ispartofReproductive Toxicology
dc.relation.ispartofsjr0,846
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectBetamethasone
dc.subjectFertility
dc.subjectReproductive programming
dc.subjectSertoli cell
dc.subjectSexual development
dc.subjectTestis
dc.titleAlterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programmingen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0003-3711-811X[1]
unesp.author.orcid0000-0002-6566-783X[10]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentMorfologia - IBBpt

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