Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin

Detalhes bibliográficos
Autor(a) principal: de Lima e Silva, Tássia C. [UNESP]
Data de Publicação: 2017
Outros Autores: da Silveira, Livia T. R. [UNESP], Fragoso, Mariana F. [UNESP], da Silva, Flávia R. M. [UNESP], Martinez, Meire F. [UNESP], Zapaterini, Joyce R. [UNESP], Diniz, Odair H. G. [UNESP], Scarano, Wellerson R. [UNESP], Barbisan, Luis F. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s12672-017-0304-7
http://hdl.handle.net/11449/175014
Resumo: 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) presents adverse effects on breast development/carcinogenesis. This study aimed to identify the ability of resveratrol (Res) to modify the adverse effects of TCDD in a female offspring. Pregnant female Wistar rats were allocated into four groups: TCDD, TCDD + Res, Res, and control. TCDD (1 μg/kg) was orally administered as a single dose on gestational day (GD) 15, and Res was orally administered during GD10–21 and lactation at a dose of 20 mg/kg/day. Female offsprings were euthanized on a specific postnatal day (PND) for hormonal analysis (PND 22, 48–51), vaginal opening (PND 30–48), and mammary gland morphology (PND 22). Other females received two doses of N-nitroso-N-methylurea (MNU, 50 mg/kg) on PNDs 22 and 51 and were euthanized on PND 24 (Ki-67, ER-α and apoptosis indexes or molecular analysis) or PND 180 (tumor assay). TCDD exposure altered the development of the mammary structure while these alterations were partially improved by maternal Res. Two days after first MNU administration, some genes associated with apoptosis were altered in the mammary tissue from the TCDD group (Bax and Caspase 3 down- and Bcl-2 upregulated) but were also partially reestablished by maternal Res. Mammary gland bcl-2 and bcl-xl proteins expression was increased while the apoptosis index was reduced by TCDD exposure but restored by maternal Res. An increase in number of mammary tumors was observed in female offspring from the TCDD group compared to the other groups. The results indicate that most mammary changes induced in female offspring through TCDD exposure or after MNU administrations were reduced by maternal resveratrol treatment.
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spelling Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) presents adverse effects on breast development/carcinogenesis. This study aimed to identify the ability of resveratrol (Res) to modify the adverse effects of TCDD in a female offspring. Pregnant female Wistar rats were allocated into four groups: TCDD, TCDD + Res, Res, and control. TCDD (1 μg/kg) was orally administered as a single dose on gestational day (GD) 15, and Res was orally administered during GD10–21 and lactation at a dose of 20 mg/kg/day. Female offsprings were euthanized on a specific postnatal day (PND) for hormonal analysis (PND 22, 48–51), vaginal opening (PND 30–48), and mammary gland morphology (PND 22). Other females received two doses of N-nitroso-N-methylurea (MNU, 50 mg/kg) on PNDs 22 and 51 and were euthanized on PND 24 (Ki-67, ER-α and apoptosis indexes or molecular analysis) or PND 180 (tumor assay). TCDD exposure altered the development of the mammary structure while these alterations were partially improved by maternal Res. Two days after first MNU administration, some genes associated with apoptosis were altered in the mammary tissue from the TCDD group (Bax and Caspase 3 down- and Bcl-2 upregulated) but were also partially reestablished by maternal Res. Mammary gland bcl-2 and bcl-xl proteins expression was increased while the apoptosis index was reduced by TCDD exposure but restored by maternal Res. An increase in number of mammary tumors was observed in female offspring from the TCDD group compared to the other groups. The results indicate that most mammary changes induced in female offspring through TCDD exposure or after MNU administrations were reduced by maternal resveratrol treatment.Departamento de Enfermagem Centro Acadêmico de Vitória UFPE– Universidade Federal do Pernambuco (UFPE)Departamento de Patologia Faculdade de Medicina de Botucatu Universidade Estadual Paulista (UNESP)Departamento de Morfologia Instituto de Biociências de Botucatu Universidade Estadual Paulista (UNESP)Departamento de Patologia Faculdade de Medicina de Botucatu Universidade Estadual Paulista (UNESP)Departamento de Morfologia Instituto de Biociências de Botucatu Universidade Estadual Paulista (UNESP)Universidade Federal de Pernambuco (UFPE)Universidade Estadual Paulista (Unesp)de Lima e Silva, Tássia C. [UNESP]da Silveira, Livia T. R. [UNESP]Fragoso, Mariana F. [UNESP]da Silva, Flávia R. M. [UNESP]Martinez, Meire F. [UNESP]Zapaterini, Joyce R. [UNESP]Diniz, Odair H. G. [UNESP]Scarano, Wellerson R. [UNESP]Barbisan, Luis F. [UNESP]2018-12-11T17:13:51Z2018-12-11T17:13:51Z2017-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article286-297application/pdfhttp://dx.doi.org/10.1007/s12672-017-0304-7Hormones and Cancer, v. 8, n. 5-6, p. 286-297, 2017.1868-85001868-8497http://hdl.handle.net/11449/17501410.1007/s12672-017-0304-72-s2.0-850269042642-s2.0-85026904264.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengHormones and Cancer1,2511,251info:eu-repo/semantics/openAccess2023-12-10T06:21:09Zoai:repositorio.unesp.br:11449/175014Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-10T06:21:09Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin
title Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin
spellingShingle Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin
de Lima e Silva, Tássia C. [UNESP]
title_short Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin
title_full Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin
title_fullStr Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin
title_full_unstemmed Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin
title_sort Maternal Resveratrol Treatment Reduces the Risk of Mammary Carcinogenesis in Female Offspring Prenatally Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin
author de Lima e Silva, Tássia C. [UNESP]
author_facet de Lima e Silva, Tássia C. [UNESP]
da Silveira, Livia T. R. [UNESP]
Fragoso, Mariana F. [UNESP]
da Silva, Flávia R. M. [UNESP]
Martinez, Meire F. [UNESP]
Zapaterini, Joyce R. [UNESP]
Diniz, Odair H. G. [UNESP]
Scarano, Wellerson R. [UNESP]
Barbisan, Luis F. [UNESP]
author_role author
author2 da Silveira, Livia T. R. [UNESP]
Fragoso, Mariana F. [UNESP]
da Silva, Flávia R. M. [UNESP]
Martinez, Meire F. [UNESP]
Zapaterini, Joyce R. [UNESP]
Diniz, Odair H. G. [UNESP]
Scarano, Wellerson R. [UNESP]
Barbisan, Luis F. [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Pernambuco (UFPE)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv de Lima e Silva, Tássia C. [UNESP]
da Silveira, Livia T. R. [UNESP]
Fragoso, Mariana F. [UNESP]
da Silva, Flávia R. M. [UNESP]
Martinez, Meire F. [UNESP]
Zapaterini, Joyce R. [UNESP]
Diniz, Odair H. G. [UNESP]
Scarano, Wellerson R. [UNESP]
Barbisan, Luis F. [UNESP]
description 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) presents adverse effects on breast development/carcinogenesis. This study aimed to identify the ability of resveratrol (Res) to modify the adverse effects of TCDD in a female offspring. Pregnant female Wistar rats were allocated into four groups: TCDD, TCDD + Res, Res, and control. TCDD (1 μg/kg) was orally administered as a single dose on gestational day (GD) 15, and Res was orally administered during GD10–21 and lactation at a dose of 20 mg/kg/day. Female offsprings were euthanized on a specific postnatal day (PND) for hormonal analysis (PND 22, 48–51), vaginal opening (PND 30–48), and mammary gland morphology (PND 22). Other females received two doses of N-nitroso-N-methylurea (MNU, 50 mg/kg) on PNDs 22 and 51 and were euthanized on PND 24 (Ki-67, ER-α and apoptosis indexes or molecular analysis) or PND 180 (tumor assay). TCDD exposure altered the development of the mammary structure while these alterations were partially improved by maternal Res. Two days after first MNU administration, some genes associated with apoptosis were altered in the mammary tissue from the TCDD group (Bax and Caspase 3 down- and Bcl-2 upregulated) but were also partially reestablished by maternal Res. Mammary gland bcl-2 and bcl-xl proteins expression was increased while the apoptosis index was reduced by TCDD exposure but restored by maternal Res. An increase in number of mammary tumors was observed in female offspring from the TCDD group compared to the other groups. The results indicate that most mammary changes induced in female offspring through TCDD exposure or after MNU administrations were reduced by maternal resveratrol treatment.
publishDate 2017
dc.date.none.fl_str_mv 2017-12-01
2018-12-11T17:13:51Z
2018-12-11T17:13:51Z
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/10.1007/s12672-017-0304-7
Hormones and Cancer, v. 8, n. 5-6, p. 286-297, 2017.
1868-8500
1868-8497
http://hdl.handle.net/11449/175014
10.1007/s12672-017-0304-7
2-s2.0-85026904264
2-s2.0-85026904264.pdf
url http://dx.doi.org/10.1007/s12672-017-0304-7
http://hdl.handle.net/11449/175014
identifier_str_mv Hormones and Cancer, v. 8, n. 5-6, p. 286-297, 2017.
1868-8500
1868-8497
10.1007/s12672-017-0304-7
2-s2.0-85026904264
2-s2.0-85026904264.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Hormones and Cancer
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1,251
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 286-297
application/pdf
dc.source.none.fl_str_mv Scopus
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collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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