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Mutagenic and cytotoxic activity of an isocoumarin (paepalantine) isolated from Paepalanthus vellozioides

dc.contributor.authorVaranda, Eliana Aparecida [UNESP]
dc.contributor.authorRaddi, Maria Stella Gonçalves
dc.contributor.authorDe Luz Dias, Francisca
dc.contributor.authorAraújo, Maria Cristina P.
dc.contributor.authorGibran, Solange Cardoso Alvares
dc.contributor.authorTakahashi, Catarina S.
dc.contributor.authorVilegas, Wagner
dc.contributor.institutionEstadual Paulist University
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de Pernambuco (UFPE)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2022-04-28T19:53:23Z
dc.date.available2022-04-28T19:53:23Z
dc.date.issued1997-09-03
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 μg/plate. The mutagenicity was confirmed in assays with CHO cells treated in the G1, S, and G2 phases of the cell cycle. There was an increase in the chromosomal aberration frequency, mainly in the G2 phase. Furthermore, the mitotic index of the treated cultures (40, 80, and 160 μg/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 μg/ml, respectively. Alterations to the paepalantine structure are suggested to reduce its mutagenic and cytotoxic activity in investigations for its antineoplasic potential.en
dc.description.affiliationFac. Pharmaceutical Sci. Araraquara Estadual Paulist University, São Paulo
dc.description.affiliationFac. of Med. of Ribeirão Preto São Paulo University, São Paulo
dc.description.affiliationFac. Philos., Sci., Letters R. São Paulo University, São Paulo
dc.description.affiliationDepartment of Genetics Federal University of Pernambuco, Pernambuco
dc.description.affiliationChemical Institute of Araraquara Estadual Paulist University, São Paulo
dc.description.affiliationFaculdade de Cie. Farmaceuticas UNESP Depto. de Cie. Biológicas, Rodovia Araraquara-Jaú. Km 1, CEP 14801-9O2, Araraquara, Sao Paulo
dc.description.affiliationUnespFaculdade de Cie. Farmaceuticas UNESP Depto. de Cie. Biológicas, Rodovia Araraquara-Jaú. Km 1, CEP 14801-9O2, Araraquara, Sao Paulo
dc.format.extent85-95
dc.identifierhttp://dx.doi.org/10.1002/(SICI)1520-6866(1997)17:2<85
dc.identifier.citationTeratogenesis Carcinogenesis and Mutagenesis, v. 17, n. 2, p. 85-95, 1997.
dc.identifier.doi10.1002/(SICI)1520-6866(1997)17:2<85
dc.identifier.issn0270-3211
dc.identifier.scopus2-s2.0-0003056968
dc.identifier.urihttp://hdl.handle.net/11449/223852
dc.language.isoeng
dc.relation.ispartofTeratogenesis Carcinogenesis and Mutagenesis
dc.sourceScopus
dc.subjectAmes test
dc.subjectChromosomal aberrations
dc.subjectCytotoxicity
dc.subjectIsocoumarin
dc.subjectPaepalantine
dc.titleMutagenic and cytotoxic activity of an isocoumarin (paepalantine) isolated from Paepalanthus vellozioidesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
unesp.departmentCiências Biológicas - FCFpt

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