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Diuron-Induced Rat Bladder Epithelial Cytotoxicity

dc.contributor.authorDa Rocha, Mitscheli S. [UNESP]
dc.contributor.authorArnold, Lora L.
dc.contributor.authorPennington, Karen L.
dc.contributor.authorMuirhead, David
dc.contributor.authorDodmane, Puttappa R.
dc.contributor.authorAnwar, Muhammad M.
dc.contributor.authorBattalora, Michael
dc.contributor.authorCamargo, João Lauro Viana de [UNESP]
dc.contributor.authorCohen, Samuel Monroe [UNESP]
dc.contributor.institutionUniv Nebraska Med Ctr
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionDuPont Crop Protect
dc.date.accessioned2014-05-20T13:37:32Z
dc.date.available2014-05-20T13:37:32Z
dc.date.issued2012-12-01
dc.description.abstractDiuron, a substituted urea herbicide, is carcinogenic to the rat urinary bladder at high dietary levels (2500 ppm). To further elucidate the mode of action, this study aimed to determine the time course and sequence of bladder cytotoxic and proliferative changes induced by diuron treatment of male Wistar rats. Rats were randomized into two groups (control and 2500 ppm diuron) and treated for 28 days. Ten rats from each group were terminated on each of study days 1, 3, 7, or 28. Scanning electron micro scopy (SEM) showed urothelial cell swelling beginning on day 1, and by day 28, showed extensive necrosis, exfoliation and piling up of cells suggestive of hyperplasia. No difference in the bromo deoxyuridine labeling index was detected. In a second experiment, rats were randomized into control and diuron-treated groups and treated for 7 days or 8 weeks. After 7 days, transmission electron microscopy showed cell degenerative changes and distention of the cytoplasm, organelles, and nuclei characteristic of cytolysis. This resulted in protrusion of the superficial cells into the lumen, corresponding to the cell swelling observed previously by SEM. After 8 weeks, bladders in the diuron-treated group showed an increased incidence of simple hyperplasia by light microscopy (6/10, p < 0.05) compared with controls (0/10) and a significantly different SEM classification. In summary, our results support the hypothesis that urothelial cytotoxicity followed by regenerative cell proliferation are the sequential key events that occur with high-dose diuron exposure in rats.en
dc.description.affiliationUniv Nebraska Med Ctr, Dept Pathol & Microbiol, Omaha, NE 68198 USA
dc.description.affiliationUNESP São Paulo State Univ, Botucatu Med Sch, Dept Pathol, Ctr Evaluat Environm Impact Human Hlth TOXICAM, São Paulo, Brazil
dc.description.affiliationDuPont Crop Protect, Newark, DE USA
dc.description.affiliationUnespUNESP São Paulo State Univ, Botucatu Med Sch, Dept Pathol, Ctr Evaluat Environm Impact Human Hlth TOXICAM, São Paulo, Brazil
dc.description.sponsorshipDuPont Crop Protection
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.format.extent281-288
dc.identifierhttp://dx.doi.org/10.1093/toxsci/kfs256
dc.identifier.citationToxicological Sciences. Oxford: Oxford Univ Press, v. 130, n. 2, p. 281-288, 2012.
dc.identifier.doi10.1093/toxsci/kfs256
dc.identifier.issn1096-6080
dc.identifier.urihttp://hdl.handle.net/11449/13001
dc.identifier.wosWOS:000311307600007
dc.language.isoeng
dc.publisherOxford University Press
dc.relation.ispartofToxicological Sciences
dc.relation.ispartofjcr4.181
dc.relation.ispartofsjr1,538
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectDiuronen
dc.subjecturinary bladderen
dc.subjectcytotoxicityen
dc.subjectproliferationen
dc.subjectmorphologyen
dc.subjectelectron microscopyen
dc.titleDiuron-Induced Rat Bladder Epithelial Cytotoxicityen
dc.typeArtigo
dcterms.licensehttp://www.oxfordjournals.org/access_purchase/self-archiving_policyb.html
dcterms.rightsHolderOxford Univ Press
dspace.entity.typePublication
unesp.author.orcid0000-0001-9953-3226[5]
unesp.author.orcid0000-0003-0477-2887[5]
unesp.author.orcid0000-0003-3833-4172[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentPatologia - FMBpt

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