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Sexual maturation and fertility of mice exposed to triphenyltin during prepubertal and pubertal periods

dc.contributor.authorMello, Marcia S. Campos
dc.contributor.authorDelgado, Isabella F.
dc.contributor.authorFavareto, Ana Paula A. [UNESP]
dc.contributor.authorLopes, Camila M. T.
dc.contributor.authorBatista, Marcelo M.
dc.contributor.authorKempinas, Wilma De-Grava [UNESP]
dc.contributor.authorPaumgartten, Francisco J. R.
dc.contributor.institutionNatl Sch Publ Hlth
dc.contributor.institutionNatl Inst Hlth Qual Control
dc.contributor.institutionFiocruz MS
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniv Fed Estado Rio de Janeiro
dc.date.accessioned2018-11-26T22:40:54Z
dc.date.available2018-11-26T22:40:54Z
dc.date.issued2015-01-01
dc.description.abstractThis study investigated the effects of pre- and peripubertal exposure (PND 15-45) to triphenyltin hydroxide (TPT: 0, 1.875, 3.75, 7.5 and 15 mg/kg bw/d po) on mouse sexual maturation and fertility. Half of the mice were euthanized on PND 46 and the remaining mice were submitted to fertility tests on PND 65-75. TPT caused a transient decrease of weight gain at 3.75 mg/kg bw/d, and deaths and body weight deficits at higher doses. Delays of testes descent (TD), vaginal opening (VO) and first estrus (FE) occurred at doses >3.75 (TD) and >= 7.5 mg/kg bw/d (VO, FE), respectively. Body weight on the days of TD, VO and FE did not differ among groups. TPT at doses >= 3.75 mg/kg decreased sperm and spermatid counts at the end of treatment (PND 46) but no alteration was noted later on PND 75. Testicular histopathology (PND 46) showed a dose-dependent reduction of seminiferous tubules diameter, a greater degree of vacuolation in Sertoli cells and germ cell degeneration and necrosis in TPT-treated mice. TPT did not affect the outcome of fertility tests. Study-derived NOAEL was 1.875 mg TPT/kg bw/d for males and 3.75 mg TPT/kg bw/d for females. The detrimental effects of TPT on spermatogenesis were reversed after treatment discontinuation. (C) 2014 The Authors. Published by Elsevier Ireland Ltd. This is an open access article under the CC BY-NC-ND license.en
dc.description.affiliationNatl Sch Publ Hlth, Dept Biol Sci, Lab Environm Toxicol, Rio De Janeiro, Brazil
dc.description.affiliationNatl Inst Hlth Qual Control, Dept Immunol, Rio De Janeiro, Brazil
dc.description.affiliationFiocruz MS, Oswaldo Cruz Fdn, BR-21045900 Rio De Janeiro, RJ, Brazil
dc.description.affiliationState Univ Sao Paulo UNESP, Dept Morphol, Sao Paulo, Brazil
dc.description.affiliationUniv Fed Estado Rio de Janeiro, UNIRIO, Dept Biochem, Rio De Janeiro, Brazil
dc.description.affiliationUnespState Univ Sao Paulo UNESP, Dept Morphol, Sao Paulo, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ)
dc.description.sponsorshipFIOCRUZ (PAPES-III)
dc.format.extent405-414
dc.identifierhttp://dx.doi.org/10.1016/j.toxrep.2014.12006
dc.identifier.citationToxicology Reports. Amsterdam: Elsevier Science Bv, v. 2, p. 405-414, 2015.
dc.identifier.doi10.1016/j.toxrep.2014.12006
dc.identifier.fileWOS000218510700045.pdf
dc.identifier.issn2214-7500
dc.identifier.urihttp://hdl.handle.net/11449/164851
dc.identifier.wosWOS:000218510700045
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofToxicology Reports
dc.relation.ispartofsjr0,580
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectTriphenyltin
dc.subjectTPTH
dc.subjectOrganotin compounds
dc.subjectPuberty
dc.subjectPostnatal exposure
dc.subjectFertility
dc.titleSexual maturation and fertility of mice exposed to triphenyltin during prepubertal and pubertal periodsen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt
unesp.departmentMorfologia - IBBpt

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