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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/13018
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dc.contributor.authorBidinotto, Lucas T.-
dc.contributor.authorCosta, Celso A. R. A.-
dc.contributor.authorSalvadori, Daisy Maria Favero-
dc.contributor.authorCosta, Mirtes-
dc.contributor.authorRodrigues, Maria Aparecida Marchesan-
dc.contributor.authorBarbisan, Luis Fernando-
dc.date.accessioned2014-05-20T13:37:34Z-
dc.date.accessioned2016-10-25T16:54:13Z-
dc.date.available2014-05-20T13:37:34Z-
dc.date.available2016-10-25T16:54:13Z-
dc.date.issued2011-08-01-
dc.identifierhttp://dx.doi.org/10.1002/jat.1593-
dc.identifier.citationJournal of Applied Toxicology. Hoboken: Wiley-blackwell, v. 31, n. 6, p. 536-544, 2011.-
dc.identifier.issn0260-437X-
dc.identifier.urihttp://hdl.handle.net/11449/13018-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/13018-
dc.description.abstractThis study investigated the protective effect of oral treatment with lemongrass (Cymbopogon citratus STAPF) essential oil (LGEO) on leukocyte DNA damage induced by N-methyl-N-nitrosurea (MNU). Also, the anticarcinogenic activity of LGEO was investigated in a multi-organ carcinogenesis bioassay induced by 7,12-dimethylbenz(a)antracene, 1,2-dimethylhydrazine and N-butyl-N-(4-hydroxibuthyl)nitrosamine in Balb/C female Balb/c mice (DDB-initiated mice). In the short-term study, the animals were allocated into three groups: vehicle group (negative control), MNU group (positive control) and LGEO 500 mg kg(-1) (five times per week for 5 weeks) plus MNU group (test group). Blood samples were collected to analyze leukocyte DNA damage by comet assay 4 h after each MNU application at the end of weeks 3 and 5. The LGEO 500 mg kg(-1) treated group showed significantly lower (P < 0.01) leukocyte DNA damage than its respective positive group exposed to MNU alone at week 3. In the medium-term study, DDB-initiated mice were allocated into three groups: vehicle group (positive control) and LGEO 125 or 500 mg kg(-1) (five times per week for 6 weeks; test groups). At week 20, all animals were euthanized and mammary glands, colon and urinary bladder were processed for histopathological analyses for detection of preneoplastic and neoplastic lesions. A slight non-significant effect of treatment with LGEO 500 mg kg(-1) in reducing development of alveolar and ductal mammary hyperplasia was found (P = 0.075). Our findings indicate that lemongrass essential oil provided protective action against MNU-induced DNA damage and a potential anticarcinogenic activity against mammary carcinogenesis in DDB-initiated female Balb/C mice. Copyright (C) 2010 John Wiley & Sons, Ltd.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent536-544-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.sourceWeb of Science-
dc.subjectlemongrass essential oilen
dc.subjectantigenotoxicityen
dc.subjectanticarcinogenesisen
dc.subjectmultiple-organ carcinogenesisen
dc.subjectfemale Balb/c miceen
dc.titleProtective effects of lemongrass (Cymbopogon citratus STAPF) essential oil on DNA damage and carcinogenesis in female Balb/C miceen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Estadual Paulista, UNESP, São Paulo State Univ, Dept Morphol,Inst Biosci, BR-18618970 Botucatu, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, UNESP, Fac Med, Dept Patol, BR-18618970 Botucatu, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, UNESP, Inst Biociencias, Dept Farmacol, BR-18618970 Botucatu, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, São Paulo State Univ, Dept Morphol,Inst Biosci, BR-18618970 Botucatu, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, Fac Med, Dept Patol, BR-18618970 Botucatu, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, UNESP, Inst Biociencias, Dept Farmacol, BR-18618970 Botucatu, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 06/58174-0-
dc.description.sponsorshipIdFAPESP: 06/07195-8-
dc.identifier.doi10.1002/jat.1593-
dc.identifier.wosWOS:000294744900005-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Applied Toxicology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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