Alterations in male rats following in utero exposure to betamethasone suggests changes in reproductive programming
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , , , , |
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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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/openAccess2024-10-14T19:20:39Zoai:repositorio.unesp.br:11449/173105Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-10-14T19:20:39Repositório 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 |
repositoriounesp@unesp.br |
_version_ |
1826304599692148736 |