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Protective effects of beta-glucan extracted from barley against benzo[a]pyrene-induced DNA damage in hepatic cell HepG2

dc.contributor.authorAngeli, Jose Pedro F.
dc.contributor.authorRibeiro, Lúcia Regina [UNESP]
dc.contributor.authorAngeli, Jose Lourenco F.
dc.contributor.authorMantovani, Mario S.
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:55:48Z
dc.date.available2014-05-20T13:55:48Z
dc.date.issued2009-01-01
dc.description.abstractThe aim of the present study was to assess the genotoxic and antigenotoxic effect of beta-glucan (BG) extracted from barley. The genotoxicity of BG was tested in the single-cell gel electrophoresis assays (SCGE)/HepG2 test system. Moreover. the protective effects of BG against the genotoxicity of B[a]P were studied to delineate its mechanism of antigenotoxicity using four different treatment protocols - pre-treatment, simultaneous simple, simultaneous with pre-incubation. and post-treatment. The results showed that the compound itself was devoid of mutagenic activity at the three lower concentrations studied (1, 5, and 25 mu g/mL) however, genotoxic and cytotoxic effects were seen at 100 and 200 mu g/mL, respectively. In combination experiments with B[a]P, pronounced inhibition of DNA Migration in the SCGE assay was observed in the two simultaneous treatments, and a smaller reduction was observed in the two other treatments. Thus, the data suggest that BG acts through binding to the genotoxic compound or capturing free radicals produced during its activation. However, the protective effects observed with pre-treatment and post-treatment suggest that the BG may be modulating cell metabolism. (C) 2008 Elsevier GmbH. All rights reserved.en
dc.description.affiliationUniversidade Estadual de Londrina (UEL), Dept Biol Geral, BR-86051990 Londrina, PR, Brazil
dc.description.affiliationUNESP, Depto Biol, Programa Posgrad Biol Celular & Mol, Rio Claro, SP, Brazil
dc.description.affiliationUNESP, Fac Med, Programa Posgrad Patol, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, Depto Biol, Programa Posgrad Biol Celular & Mol, Rio Claro, SP, Brazil
dc.description.affiliationUnespUNESP, Fac Med, Programa Posgrad Patol, Botucatu, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação Araucária de Apoio ao Desenvolvimento Científico e Tecnológico do Paraná (FAADCT/PR)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.format.extent83-89
dc.identifierhttp://dx.doi.org/10.1016/j.etp.2008.05.003
dc.identifier.citationExperimental and Toxicologic Pathology. Jena: Elsevier Gmbh, Urban & Fischer Verlag, v. 61, n. 1, p. 83-89, 2009.
dc.identifier.doi10.1016/j.etp.2008.05.003
dc.identifier.issn0940-2993
dc.identifier.urihttp://hdl.handle.net/11449/19987
dc.identifier.wosWOS:000263254600010
dc.language.isoeng
dc.publisherElsevier Gmbh, Urban & Fischer Verlag
dc.relation.ispartofExperimental and Toxicologic Pathology
dc.relation.ispartofjcr2.023
dc.relation.ispartofsjr0,551
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectbeta-Glucanen
dc.subjectComet assayen
dc.subjectHepG2en
dc.subjectAntigenotoxicityen
dc.titleProtective effects of beta-glucan extracted from barley against benzo[a]pyrene-induced DNA damage in hepatic cell HepG2en
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier Gmbh, Urban & Fischer Verlag
dspace.entity.typePublication
unesp.author.orcid0000-0001-5268-6508[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Rio Claropt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentPatologia - FMBpt
unesp.departmentBiologia - IBpt

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