You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/37957
Full metadata record
DC FieldValueLanguage
dc.contributor.authorVaranda, Eliana Aparecida-
dc.contributor.authorRaddi, MSG-
dc.contributor.authorDias, F. D.-
dc.contributor.authorAraujo, MCP-
dc.contributor.authorGibran, SCA-
dc.contributor.authorTakahashi, C. S.-
dc.contributor.authorVilegas, Wagner-
dc.date.accessioned2014-05-20T15:28:04Z-
dc.date.accessioned2016-10-25T18:03:03Z-
dc.date.available2014-05-20T15:28:04Z-
dc.date.available2016-10-25T18:03:03Z-
dc.date.issued1997-01-01-
dc.identifierhttp://dx.doi.org/10.1002/(SICI)1520-6866(1997)17:2<85-
dc.identifier.citationTeratogenesis Carcinogenesis and Mutagenesis. New York: Wiley-liss, v. 17, n. 2, p. 85-95, 1997.-
dc.identifier.issn0270-3211-
dc.identifier.urihttp://hdl.handle.net/11449/37957-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/37957-
dc.description.abstractA new isocoumarin with antimicrobial activity was isolated from Paepalanthus vellozioides (a native Brazilian plant) and called paepalantine. This study was carried out to assess the mutagenic activity of this new agent in assays with Salmonella typhimurium TA100, TA98, and TA102 and in Chinese hamster ovary (CHO) cell cultures, as well as cytotoxicity to McCoy cells. Paepalantine caused a significant dose-dependent increase in the frequency of revertants in the three strains used in the assay, both with and without S9 mix, in concentrations varying from 2 to 128 mu g/ plate. The mutagenicity was confirmed in assays with CHO cells treated in the G(1), S, and G(2) phases of the cell cycle. There was an increase in the chromosomal aberration frequency, mainly in the G(2) phase. Furthermore, the mitotic index of the treated cultures (40,80, and 160 mu g/ml) was significantly lower, indicating cytotoxicity. The midpoint cytotoxicity values to McCoy cells by the neutral red (NR) and microculture tetrazolium (MTT) techniques resulted in a NR50, and MTT50 of 30 and 38 mu g/ml, respectively. Alterations to the paepalantine structure are suggested to reduce its mutagenic and cytotoxic activity in investigations for its antineoplasic potential (C) 1997 Wiley-Liss, Inc.en
dc.format.extent85-95-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.sourceWeb of Science-
dc.subjectpaepalantinept
dc.subjectchromosomal aberrationspt
dc.subjectcytotoxicitypt
dc.subjectAmes testpt
dc.subjectisocoumarinpt
dc.titleMutagenic and cytotoxic activity of an isocoumarin (Paepalantine) isolated from Paepalanthus vellozioidesen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Federal de Pernambuco (UFPE)-
dc.description.affiliationUNIV ESTADUAL PAULISTA,FAC PHARMACEUT SCI ARARAQUARA,BR-01405 SAO PAULO,BRAZIL-
dc.description.affiliationUNIV SAO PAULO,FAC MED RIBEIRAO PRETO,SAO PAULO,BRAZIL-
dc.description.affiliationUNIV SAO PAULO,FAC PHILOSOPHY SCI & LETTERS RIBEIRAO PRETO,SAO PAULO,BRAZIL-
dc.description.affiliationUNIV FED PERNAMBUCO,DEPT GENET,RECIFE,PE,BRAZIL-
dc.description.affiliationUNIV ESTADUAL PAULISTA,CHEM INST ARARAQUARA,BR-01405 SAO PAULO,BRAZIL-
dc.description.affiliationUnespUNIV ESTADUAL PAULISTA,FAC PHARMACEUT SCI ARARAQUARA,BR-01405 SAO PAULO,BRAZIL-
dc.description.affiliationUnespUNIV ESTADUAL PAULISTA,CHEM INST ARARAQUARA,BR-01405 SAO PAULO,BRAZIL-
dc.identifier.doi10.1002/(SICI)1520-6866(1997)17:2<85-
dc.identifier.wosWOS:A1997XN84000004-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofTeratogenesis Carcinogenesis and Mutagenesis-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.