Publicação:
Effect of the dibenzylbutyrolactone lignan (-)-hinokinin on doxorubicin and methyl methanesulfonate clastogenicity in V79 Chinese hamster lung fibroblasts

dc.contributor.authorResende, Flavia Aparecida [UNESP]
dc.contributor.authorTomazella, Iara Maluf
dc.contributor.authorBarbosa, Lilian Cristina
dc.contributor.authorPonce, Marina
dc.contributor.authorFurtado, Ricardo Andrade
dc.contributor.authorPereira, Ana Carolina
dc.contributor.authorBastos, Jairo Kenupp
dc.contributor.authorAndrade e Silva, Marcio Luis
dc.contributor.authorTavares, Denise Crispim
dc.contributor.institutionUniv Franca
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T15:33:41Z
dc.date.available2014-05-20T15:33:41Z
dc.date.issued2010-07-19
dc.description.abstractThe dibenzylbutyrolactone lignan (-)-hinokinin (HK) was obtained by partial synthesis from (-)-cubebin, isolated from the dry seeds of the pepper, Piper cubeba. In view of the trypanocidal activity of HK and its potential as a lead compound for drug development, evaluation of its possible genotoxic activity is required. We have tested HK for possible genotoxicity and evaluated the compound's effect on the activity of the clastogens doxorubicin (DXR) and methyl methanesulfonate (MMS) in the micronucleus (MN) assay with Chinese hamster lung fibroblast V79 cells. HK alone did not induce MN, at concentrations up to 128 mu M. In combined treatments, HK reduced the frequency of MN induced by MMS. With respect to DXR, HK exerted a protective effect at lower concentrations, but at higher concentrations it potentiated DXR clastogenicity. (C) 2010 Elsevier B.V. All rights reserved.en
dc.description.affiliationUniv Franca, BR-14404600 São Paulo, Brazil
dc.description.affiliationUniv Estadual Paulista, Fac Ciencias Farmaceut Araraquara, BR-14801902 São Paulo, Brazil
dc.description.affiliationUniv São Paulo, Fac Ciencias Farmaceut Ribeirao Preto, BR-14040903 São Paulo, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Fac Ciencias Farmaceut Araraquara, BR-14801902 São Paulo, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 07/07211-6
dc.format.extent62-66
dc.identifierhttp://dx.doi.org/10.1016/j.mrgentox.2010.04.023
dc.identifier.citationMutation Research-genetic Toxicology and Environmental Mutagenesis. Amsterdam: Elsevier B.V., v. 700, n. 1-2, p. 62-66, 2010.
dc.identifier.doi10.1016/j.mrgentox.2010.04.023
dc.identifier.issn1383-5718
dc.identifier.urihttp://hdl.handle.net/11449/42248
dc.identifier.wosWOS:000280219000009
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofMutation Research: Genetic Toxicology and Environmental Mutagenesis
dc.relation.ispartofjcr1.996
dc.relation.ispartofsjr0,747
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectHinokininen
dc.subjectMicronucleusen
dc.subjectV79 cellen
dc.subjectClastogenicityen
dc.titleEffect of the dibenzylbutyrolactone lignan (-)-hinokinin on doxorubicin and methyl methanesulfonate clastogenicity in V79 Chinese hamster lung fibroblastsen
dc.typeResumo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication

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