Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/12479
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dc.contributor.authorMello, Marcia Sarpa de Campos-
dc.contributor.authorCarvalho, Rosângela Ribeiro de-
dc.contributor.authorDelgado, Isabella Fernandes-
dc.contributor.authorPaumgartten, Francisco José Roma-
dc.date.accessioned2023-01-25T17:12:28Z-
dc.date.available2023-01-25T17:12:28Z-
dc.date.issued2007-
dc.identifier.issn0273-2300-
dc.identifier.urihttps://ninho.inca.gov.br/jspui/handle/123456789/12479-
dc.description.abstractTriphenyltin-hydroxide (TPTH) is used as agricultural fungicide in Brazil and elsewhere. This study was undertaken to evaluate the developmental toxicity of TPTH in mice. Swiss Webster mice were treated by gavage with TPTH (0, 3.75, 7.5, 15 and 30 mg/kg bw/day) on gestation days (GD) 6–17. Caesarean sections were performed on GD 18, and implantations, resorptions and live and dead fetuses were counted. Half of each litter was fixed and examined for visceral anomalies while the remaining fetuses were cleared and stained with Alizarin Red S for skeleton evaluation. A reduced pregnancy weight gain (after subtraction of uterine weights), smaller thymus, spleen and liver, and deaths indicated that doses P7.5 mg/kg body wt/day were toxic to mothers. At the two highest doses, TPTH enhanced embryolethality and reduced fetal body weight. The incidence of cleft palate (not seen in controls) was augmented (36.8%) at the highest dose of TPTH, while palatine bone defects were increased at the lowest dose (3.75 mg/kg bw/day). Soft-tissue anomalies, such as mis shapened thymus, and malpositioned testes and uteri, were more frequent at doses of TPTH P7.5 mg/kg bw/day. TPTH also caused a dose-related increase of fetal skeleton variations (e.g. poorly ossified skull bones) and malformations (misshapened Axis and skull bones). In conclusion, TPTH was toxic to the embryos (NOAEL <3.75 mg/kg bw/day) at doses that were not overtly toxic to their motherspt_BR
dc.publisherRegulatory Toxicology and Pharmacology 49 (2007) 43–52pt_BR
dc.subjectCompostos de Terfenilpt_BR
dc.subjectTerphenyl Compoundspt_BR
dc.subjectFentanilapt_BR
dc.subjectFentanylpt_BR
dc.subjectTeriparatidapt_BR
dc.subjectTeriparatidept_BR
dc.subjectCompostos Orgânicos de Estanhopt_BR
dc.subjectOrganotin Compoundspt_BR
dc.subjectToxicidadept_BR
dc.subjectToxicitypt_BR
dc.subjectCuidado Pré-Natalpt_BR
dc.subjectPrenatal Carept_BR
dc.subjectDesenvolvimento Embrionário e Fetalpt_BR
dc.subjectEmbryonic and Fetal Developmentpt_BR
dc.subjectAnormalidades Teratoides Gravespt_BR
dc.subjectAbnormalities Severe Teratoidpt_BR
dc.subjectTeratógenospt_BR
dc.subjectTeratogenspt_BR
dc.titleDevelopmental toxicity of triphenyltin hydroxide in micept_BR
dc.TypeArticlept_BR
Appears in Collections:Artigos de Periódicos da área da Vigilância do Câncer Relacionado ao Trabalho e ao Ambiente
Marcia Sarpa de Campos Mello

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