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Ascorbic acid co-administered with rosuvastatin reduces reproductive impairment in the male offspring from male rats exposed to the statin at pre-puberty

dc.contributor.authorLeite, Gabriel Adan Araújo [UNESP]
dc.contributor.authorFigueiredo, Thamiris Moreira [UNESP]
dc.contributor.authorGuerra, Marina Trevizan [UNESP]
dc.contributor.authorBorges, Cibele dos Santos [UNESP]
dc.contributor.authorFernandes, Fábio Henrique [UNESP]
dc.contributor.authorAnselmo-Franci, Janete Aparecida
dc.contributor.authorKempinas, Wilma De Grava [UNESP]
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2018-12-11T17:20:32Z
dc.date.available2018-12-11T17:20:32Z
dc.date.issued2018-08-01
dc.description.abstractObesity during childhood and adolescence is closely related to dysfunctions on lipid profile in children. Rosuvastatin is a statin that decreases serum total cholesterol. Ascorbic acid is an important antioxidant compound for male reproduction. Pre-pubertal male rats were distributed into six experimental groups that received saline solution 0.9% (vehicle), 3 or 10 mg/kg/day of rosuvastatin, 150 mg/day of ascorbic acid, or 3 or 10 mg/kg/day of rosuvastatin co-administered with 150 mg/day of ascorbic acid by gavage from post-natal day (PND)23 until PND53. Rats were maintained until adulthood and mated with nulliparous females to obtain the male offspring, whose animals were evaluated at adulthood in relation to reproductive parameters. This study is a follow up of a previous paper addressing potential effects on F0 generation only (Leite et al., 2017). Male offspring from rosuvastatin-exposed groups showed increased sperm DNA fragmentation, androgen depletion and impairment on the testicular and epididymal structure. Ascorbic acid coadministered to the fathers ameliorated the reproductive damage in the offspring. In summary, paternal exposure to rosuvastatin may affect the reproduction in the male offspring; however, paternal supplementation with ascorbic acid was able to reduce the reproductive impairment in the male offspring caused by statin treatment to the fathers.en
dc.description.affiliationGraduate Program in Cell and Structural Biology Institute of Biology State University of Campinas – UNICAMP
dc.description.affiliationDepartment of Morphology São Paulo State University (Unesp) Institute of Biosciences
dc.description.affiliationDepartment of Pathology São Paulo State University (Unesp) Medical School
dc.description.affiliationDepartment of Morphology Stomatology and Physiology School of Dentistry USP – University of São Paulo, Ribeirão Preto
dc.description.affiliationUnespDepartment of Morphology São Paulo State University (Unesp) Institute of Biosciences
dc.description.affiliationUnespDepartment of Pathology São Paulo State University (Unesp) Medical School
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: #013/22495-1
dc.description.sponsorshipIdFAPESP: #014/13659-3
dc.description.sponsorshipIdCNPq: 308842/2013-8
dc.format.extent416-429
dc.identifierhttp://dx.doi.org/10.1016/j.fct.2018.05.043
dc.identifier.citationFood and Chemical Toxicology, v. 118, p. 416-429.
dc.identifier.doi10.1016/j.fct.2018.05.043
dc.identifier.file2-s2.0-85047624542.pdf
dc.identifier.issn1873-6351
dc.identifier.issn0278-6915
dc.identifier.scopus2-s2.0-85047624542
dc.identifier.urihttp://hdl.handle.net/11449/176373
dc.language.isoeng
dc.relation.ispartofFood and Chemical Toxicology
dc.relation.ispartofsjr1,144
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectMale offspring
dc.subjectReproduction
dc.subjectStatin
dc.subjectToxicology
dc.subjectVitamin C
dc.titleAscorbic acid co-administered with rosuvastatin reduces reproductive impairment in the male offspring from male rats exposed to the statin at pre-pubertyen
dc.typeArtigo
unesp.author.orcid0000-0002-9437-6310 0000-0002-9437-6310[1]
unesp.author.orcid0000-0003-3711-811X[4]
unesp.author.orcid0000-0001-8047-0683[5]
unesp.author.orcid0000-0002-2112-5123[7]
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Medicina, Botucatupt
unesp.departmentPatologia - FMBpt

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