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

Detalhes bibliográficos
Autor(a) principal: Borges, Cibele S. [UNESP]
Data de Publicação: 2016
Outros Autores: Dias, Ana Flávia M.G. [UNESP], Rosa, Josiane Lima [UNESP], Silva, Patricia V. [UNESP], Silva, Raquel F. [UNESP], Barros, Aline L. [UNESP], Sanabria, Marciana [UNESP], Guerra, Marina T. [UNESP], Gregory, Mary, Cyr, Daniel G., De G. Kempinas, Wilma [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.reprotox.2016.05.021
http://hdl.handle.net/11449/173105
Resumo: Antenatal 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.
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spelling Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programmingBetamethasoneFertilityReproductive programmingSertoli cellSexual developmentTestisAntenatal 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.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Department of Morphology Institute of Biosciences Univ Estadual Paulista-UNESP, Distrito de Rubião Junior s/nLaboratory for Reproductive Toxicology INRS-Institut Armand-Frappier University of Quebec, 531 boulevard des PrairiesDepartment of Morphology Institute of Biosciences Univ Estadual Paulista-UNESP, Distrito de Rubião Junior s/nCNPq: 308842/2013-8Universidade Estadual Paulista (Unesp)University of QuebecBorges, Cibele S. [UNESP]Dias, Ana Flávia M.G. [UNESP]Rosa, Josiane Lima [UNESP]Silva, Patricia V. [UNESP]Silva, Raquel F. [UNESP]Barros, Aline L. [UNESP]Sanabria, Marciana [UNESP]Guerra, Marina T. [UNESP]Gregory, MaryCyr, Daniel G.De G. Kempinas, Wilma [UNESP]2018-12-11T17:03:39Z2018-12-11T17:03:39Z2016-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article125-134application/pdfhttp://dx.doi.org/10.1016/j.reprotox.2016.05.021Reproductive Toxicology, v. 63, p. 125-134.1873-17080890-6238http://hdl.handle.net/11449/17310510.1016/j.reprotox.2016.05.0212-s2.0-849752955572-s2.0-84975295557.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengReproductive Toxicology0,846info:eu-repo/semantics/openAccess2024-01-19T06:26:39Zoai:repositorio.unesp.br:11449/173105Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-19T06:26:39Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming
title Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming
spellingShingle Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming
Borges, Cibele S. [UNESP]
Betamethasone
Fertility
Reproductive programming
Sertoli cell
Sexual development
Testis
title_short Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming
title_full Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming
title_fullStr Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming
title_full_unstemmed Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming
title_sort Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming
author Borges, Cibele S. [UNESP]
author_facet Borges, Cibele S. [UNESP]
Dias, Ana Flávia M.G. [UNESP]
Rosa, Josiane Lima [UNESP]
Silva, Patricia V. [UNESP]
Silva, Raquel F. [UNESP]
Barros, Aline L. [UNESP]
Sanabria, Marciana [UNESP]
Guerra, Marina T. [UNESP]
Gregory, Mary
Cyr, Daniel G.
De G. Kempinas, Wilma [UNESP]
author_role author
author2 Dias, Ana Flávia M.G. [UNESP]
Rosa, Josiane Lima [UNESP]
Silva, Patricia V. [UNESP]
Silva, Raquel F. [UNESP]
Barros, Aline L. [UNESP]
Sanabria, Marciana [UNESP]
Guerra, Marina T. [UNESP]
Gregory, Mary
Cyr, Daniel G.
De G. Kempinas, Wilma [UNESP]
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
University of Quebec
dc.contributor.author.fl_str_mv Borges, Cibele S. [UNESP]
Dias, Ana Flávia M.G. [UNESP]
Rosa, Josiane Lima [UNESP]
Silva, Patricia V. [UNESP]
Silva, Raquel F. [UNESP]
Barros, Aline L. [UNESP]
Sanabria, Marciana [UNESP]
Guerra, Marina T. [UNESP]
Gregory, Mary
Cyr, Daniel G.
De G. Kempinas, Wilma [UNESP]
dc.subject.por.fl_str_mv Betamethasone
Fertility
Reproductive programming
Sertoli cell
Sexual development
Testis
topic Betamethasone
Fertility
Reproductive programming
Sertoli cell
Sexual development
Testis
description Antenatal 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.
publishDate 2016
dc.date.none.fl_str_mv 2016-08-01
2018-12-11T17:03:39Z
2018-12-11T17:03:39Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.reprotox.2016.05.021
Reproductive Toxicology, v. 63, p. 125-134.
1873-1708
0890-6238
http://hdl.handle.net/11449/173105
10.1016/j.reprotox.2016.05.021
2-s2.0-84975295557
2-s2.0-84975295557.pdf
url http://dx.doi.org/10.1016/j.reprotox.2016.05.021
http://hdl.handle.net/11449/173105
identifier_str_mv Reproductive Toxicology, v. 63, p. 125-134.
1873-1708
0890-6238
10.1016/j.reprotox.2016.05.021
2-s2.0-84975295557
2-s2.0-84975295557.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Reproductive Toxicology
0,846
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 125-134
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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