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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/74132
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dc.contributor.authorDa Silva, Ariane Fernanda-
dc.contributor.authorOliveira, Rodrigo Juliano-
dc.contributor.authorNiwa, Andressa Megumi-
dc.contributor.authorD'Epiro, Gláucia Fernanda Rocha-
dc.contributor.authorRibeiro, Lúcia Regina-
dc.contributor.authorMantovani, Mário Sérgio-
dc.date.accessioned2014-05-27T11:27:27Z-
dc.date.accessioned2016-10-25T18:40:48Z-
dc.date.available2014-05-27T11:27:27Z-
dc.date.available2016-10-25T18:40:48Z-
dc.date.issued2013-01-01-
dc.identifierhttp://dx.doi.org/10.1007/s10616-012-9448-z-
dc.identifier.citationCytotechnology, v. 65, n. 1, p. 41-48, 2013.-
dc.identifier.issn0920-9069-
dc.identifier.issn1573-0778-
dc.identifier.urihttp://hdl.handle.net/11449/74132-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74132-
dc.description.abstractβ-glucan is an important polysaccharide due to its medicinal properties of stimulating the immune system and preventing chronic diseases such as cancer. The aim of the present study was to determine the anticlastogenic effect of β-glucan in cells exposed to ultraviolet radiation (UV). Chromosome aberration assay was performed in drug-metabolizing cells (HTC) and non drug-metabolizing cells (CHO-K1 and repair-deficient CHO-xrs5), using different treatment protocols. Continuous treatment (UV + β-glucan) was not effective in reducing the DNA damage only in CHO-xrs5 cells. However, the pre-treatment protocol (β-glucan before UV exposition) was effective in reducing DNA damage only in CHO-K1 cells. In post-treatment (β-glucan after UV exposition) did not show significative anticlastogenic effects, although there was a tendency toward prevention. The data suggest that β-glucan has more than one action mechanism, being capable of exerting desmutagenic as well as bio-antimutagenic action. The findings also suggest that the presence of the xenobiotic metabolizing system can reduce the chemopreventive capacity of β-glucan. Therefore, these results indicate that β-glucan from Saccharomyces cerevisiae can be used in the prevention and/or reduction of DNA damage. © 2012 Springer Science+Business Media B.V.en
dc.format.extent41-48-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectβ-Glucan-
dc.subjectAnticlastogenicity-
dc.subjectCell culture-
dc.subjectUltraviolet radiation-
dc.subjectantimutagenic agent-
dc.subjectbeta glucan-
dc.subjectcell culture-
dc.subjectchemoprophylaxis-
dc.subjectchromosome aberration-
dc.subjectcontrolled study-
dc.subjectDNA damage-
dc.subjectdrug mechanism-
dc.subjecthuman-
dc.subjecthuman cell-
dc.subjectradiation exposure-
dc.subjectSaccharomyces cerevisiae-
dc.subjectultraviolet radiation-
dc.titleAnticlastogenic effect of β-glucan, extracted from Saccharomyces cerevisiae, on cultured cells exposed to ultraviolet radiationen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)-
dc.contributor.institutionUniversidade Federal de Mato Grosso do Sul (UFMS)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartamento de Biologia Geral Universidade Estadual de Londrina, Campus Universitário, Londrina, Paraná-
dc.description.affiliationUniversidade Federal de Mato Grosso Do sul, Campo Grande, Mato Grosso do Sul-
dc.description.affiliationDepartamento de Biologia Celular Universidade Estadual Paulista Rio Claro-
dc.description.affiliationUnespDepartamento de Biologia Celular Universidade Estadual Paulista Rio Claro-
dc.identifier.doi10.1007/s10616-012-9448-z-
dc.identifier.wosWOS:000313074500005-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofCytotechnology-
dc.identifier.scopus2-s2.0-84872319164-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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