Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-puberty
Autor(a) principal: | |
---|---|
Data de Publicação: | 2018 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1080/15287394.2018.1504702 http://hdl.handle.net/11449/180119 |
Resumo: | Dyslipidemias are occurring earlier in different countries due to the increase of obesity, bad eating habits, and sedentary lifestyle. Rosuvastatin reduces serum cholesterol; however, several studies associated statin exposure with male reproduction impairment. Ascorbic acid (AA) is an antioxidant substance that plays a protective role in the male reproductive system. Male rats were randomly divided into 6 experimental groups (n = 10), which received saline solution 0.9%, 3 or 10 mg/kg/day of rosuvastatin, 150 mg/day of AA or 3 or 10 mg/kg/day of rosuvastatin associated with 150 mg/day of AA from post-natal day (PND) 23 until PND 53. On PND 100, males were mated with non-treated female rats to obtain the female pups. The day of vaginal opening and the first estrus were assessed in the offspring. Two sets of females were euthanized on the first estrus after PND 42 and PND 75 to evaluate the histology of reproductive organs and hormone levels. A third set was used for sexual behavior and fertility test around PND 75. Female offspring from males exposed or co-exposed to the higher dose of statin exhibited a lower number of corpora lutea during puberty. On sexual maturity, the experimental group from males that were exposed to 3 mg displayed lower uterine luminal epithelium area. Paternal exposure to rosuvastatin at pre-puberty diminished uterine luminal epithelium in female offspring suggesting epigenetic changes were initiated by statin. Ascorbic acid co-administered to pre-pubertal males was able to ameliorate the reproductive damage in rat female offspring in adulthood. |
id |
UNSP_5a9158eeabf010ba8472e3f6ad6816d3 |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/180119 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
spelling |
Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-pubertyfemale offspringreproductionrosuvastatintoxicologyVitamin CDyslipidemias are occurring earlier in different countries due to the increase of obesity, bad eating habits, and sedentary lifestyle. Rosuvastatin reduces serum cholesterol; however, several studies associated statin exposure with male reproduction impairment. Ascorbic acid (AA) is an antioxidant substance that plays a protective role in the male reproductive system. Male rats were randomly divided into 6 experimental groups (n = 10), which received saline solution 0.9%, 3 or 10 mg/kg/day of rosuvastatin, 150 mg/day of AA or 3 or 10 mg/kg/day of rosuvastatin associated with 150 mg/day of AA from post-natal day (PND) 23 until PND 53. On PND 100, males were mated with non-treated female rats to obtain the female pups. The day of vaginal opening and the first estrus were assessed in the offspring. Two sets of females were euthanized on the first estrus after PND 42 and PND 75 to evaluate the histology of reproductive organs and hormone levels. A third set was used for sexual behavior and fertility test around PND 75. Female offspring from males exposed or co-exposed to the higher dose of statin exhibited a lower number of corpora lutea during puberty. On sexual maturity, the experimental group from males that were exposed to 3 mg displayed lower uterine luminal epithelium area. Paternal exposure to rosuvastatin at pre-puberty diminished uterine luminal epithelium in female offspring suggesting epigenetic changes were initiated by statin. Ascorbic acid co-administered to pre-pubertal males was able to ameliorate the reproductive damage in rat female offspring in adulthood.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Graduate Program in Cell and Structural Biology Institute of Biology State University of Campinas–UNICAMPDepartment of Morphology São Paulo State University (Unesp) Institute of BiosciencesDepartment of Morphology Physiology and Basic Pathology School of Dentistry of Ribeirão Preto USP–University of São PauloDepartment of Morphology São Paulo State University (Unesp) Institute of BiosciencesFAPESP: #014/13659-3CNPq: 308842/2013-8Universidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Leite, Gabriel Adan Araujo [UNESP]Figueiredo, Thamiris Moreira [UNESP]Pacheco, Tainá Louise [UNESP]Guerra, Marina Trevizan [UNESP]Anselmo-Franci, Janete AparecidaKempinas, Wilma De Grava [UNESP]2018-12-11T17:38:14Z2018-12-11T17:38:14Z2018-09-02info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article873-892application/pdfhttp://dx.doi.org/10.1080/15287394.2018.1504702Journal of Toxicology and Environmental Health - Part A: Current Issues, v. 81, n. 17, p. 873-892, 2018.1087-26201528-7394http://hdl.handle.net/11449/18011910.1080/15287394.2018.15047022-s2.0-850520107222-s2.0-85052010722.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Toxicology and Environmental Health - Part A: Current Issues0,8880,888info:eu-repo/semantics/openAccess2023-12-12T06:20:54Zoai:repositorio.unesp.br:11449/180119Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:09:12.306338Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-puberty |
title |
Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-puberty |
spellingShingle |
Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-puberty Leite, Gabriel Adan Araujo [UNESP] female offspring reproduction rosuvastatin toxicology Vitamin C |
title_short |
Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-puberty |
title_full |
Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-puberty |
title_fullStr |
Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-puberty |
title_full_unstemmed |
Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-puberty |
title_sort |
Reproductive outcomes in rat female offspring from male rats co-exposed to rosuvastatin and ascorbic acid during pre-puberty |
author |
Leite, Gabriel Adan Araujo [UNESP] |
author_facet |
Leite, Gabriel Adan Araujo [UNESP] Figueiredo, Thamiris Moreira [UNESP] Pacheco, Tainá Louise [UNESP] Guerra, Marina Trevizan [UNESP] Anselmo-Franci, Janete Aparecida Kempinas, Wilma De Grava [UNESP] |
author_role |
author |
author2 |
Figueiredo, Thamiris Moreira [UNESP] Pacheco, Tainá Louise [UNESP] Guerra, Marina Trevizan [UNESP] Anselmo-Franci, Janete Aparecida Kempinas, Wilma De Grava [UNESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual de Campinas (UNICAMP) Universidade Estadual Paulista (Unesp) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Leite, Gabriel Adan Araujo [UNESP] Figueiredo, Thamiris Moreira [UNESP] Pacheco, Tainá Louise [UNESP] Guerra, Marina Trevizan [UNESP] Anselmo-Franci, Janete Aparecida Kempinas, Wilma De Grava [UNESP] |
dc.subject.por.fl_str_mv |
female offspring reproduction rosuvastatin toxicology Vitamin C |
topic |
female offspring reproduction rosuvastatin toxicology Vitamin C |
description |
Dyslipidemias are occurring earlier in different countries due to the increase of obesity, bad eating habits, and sedentary lifestyle. Rosuvastatin reduces serum cholesterol; however, several studies associated statin exposure with male reproduction impairment. Ascorbic acid (AA) is an antioxidant substance that plays a protective role in the male reproductive system. Male rats were randomly divided into 6 experimental groups (n = 10), which received saline solution 0.9%, 3 or 10 mg/kg/day of rosuvastatin, 150 mg/day of AA or 3 or 10 mg/kg/day of rosuvastatin associated with 150 mg/day of AA from post-natal day (PND) 23 until PND 53. On PND 100, males were mated with non-treated female rats to obtain the female pups. The day of vaginal opening and the first estrus were assessed in the offspring. Two sets of females were euthanized on the first estrus after PND 42 and PND 75 to evaluate the histology of reproductive organs and hormone levels. A third set was used for sexual behavior and fertility test around PND 75. Female offspring from males exposed or co-exposed to the higher dose of statin exhibited a lower number of corpora lutea during puberty. On sexual maturity, the experimental group from males that were exposed to 3 mg displayed lower uterine luminal epithelium area. Paternal exposure to rosuvastatin at pre-puberty diminished uterine luminal epithelium in female offspring suggesting epigenetic changes were initiated by statin. Ascorbic acid co-administered to pre-pubertal males was able to ameliorate the reproductive damage in rat female offspring in adulthood. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-11T17:38:14Z 2018-12-11T17:38:14Z 2018-09-02 |
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/10.1080/15287394.2018.1504702 Journal of Toxicology and Environmental Health - Part A: Current Issues, v. 81, n. 17, p. 873-892, 2018. 1087-2620 1528-7394 http://hdl.handle.net/11449/180119 10.1080/15287394.2018.1504702 2-s2.0-85052010722 2-s2.0-85052010722.pdf |
url |
http://dx.doi.org/10.1080/15287394.2018.1504702 http://hdl.handle.net/11449/180119 |
identifier_str_mv |
Journal of Toxicology and Environmental Health - Part A: Current Issues, v. 81, n. 17, p. 873-892, 2018. 1087-2620 1528-7394 10.1080/15287394.2018.1504702 2-s2.0-85052010722 2-s2.0-85052010722.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Toxicology and Environmental Health - Part A: Current Issues 0,888 0,888 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
873-892 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 |
|
_version_ |
1808129165695647744 |