dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:20:22Z
dc.date.accessioned2022-10-05T17:45:15Z
dc.date.available2014-05-27T11:20:22Z
dc.date.available2022-10-05T17:45:15Z
dc.date.created2014-05-27T11:20:22Z
dc.date.issued2001-12-01
dc.identifierRevista de Ciencias Farmaceuticas, v. 22, n. 1, p. 41-56, 2001.
dc.identifier0101-3793
dc.identifierhttp://hdl.handle.net/11449/66731
dc.identifier2-s2.0-0035552072
dc.identifier7501930236496670
dc.identifier1493338692663672
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3916456
dc.description.abstractIn the last years some natural products has been described as supressors of the mutagenic process in bacteria, the antimutagenics. The literature reference that in most of the countries, the population makes use of medicinal plants. The plant Momordica charantia (Cucurbitaceae) is original from Africa being used popularly as purgative, antirheumatic and for skin problems, burns and hemorrhoids. The present work had as objective to evaluate the mutagenic and antimutagenic activities of the ethanolic extract of M. charantia in Salmonella/microsome assays using TA100, TA98 and TA102 strains. It was verified that the extract did not present mutagenic activity when evaluated in different concentrations (0.64, 1.27, 2.55 and 3.84 mg/plate) but acted as antimutagenic agent against the mutations induced by the sodium azide (TA100,-S9), 4-nitro-phenylenediamine (TA98, -S9), daunomycin (TA102, +S9) 2-anthramine (TA100 and TA98, +S9) and 2-aminofluorene (TA102, +S9). When the metabolic activation (+S9) was used, the percentage of inhibition of the mutagenicity varied in the range of 31%-96%, while in absence of metabolizing system (-S9), the maximum percentage of inhibition of the mutagenicity was 44%. In that way, we can conclude that the metabolites found in the extract has potential to protect the genetic material against the damages induced by different chemical agents.
dc.languagepor
dc.relationRevista de Ciencias Farmaceuticas
dc.rightsAcesso restrito
dc.sourceScopus
dc.subjectAmes test
dc.subjectAntimutagenic activity
dc.subjectMomordica charantia
dc.subjectS. typhimurium
dc.subject2 aminoanthracene
dc.subject2 fluorenylamine
dc.subject4 nitro 1,2 phenylenediamine
dc.subjectantimutagenic agent
dc.subjectantirheumatic agent
dc.subjectbacterial antigen
dc.subjectdaunorubicin
dc.subjectlaxative
dc.subjectMomordica charantia extract
dc.subjectmutagenic agent
dc.subjectsodium azide
dc.subjectantineoplastic activity
dc.subjectburn
dc.subjectconcentration response
dc.subjectcontrolled study
dc.subjectevaluation
dc.subjecthemorrhoid
dc.subjectinhibition kinetics
dc.subjectmedicinal plant
dc.subjectmetabolic regulation
dc.subjectmetabolite
dc.subjectmicrosome
dc.subjectmomordica charantia
dc.subjectmutagenicity
dc.subjectnonhuman
dc.subjectphytotherapy
dc.subjectplant
dc.subjectSalmonella typhimurium
dc.subjectskin disease
dc.subjectstrain identification
dc.titleAvaliação do extrato de Momordica charantia em Salmonella typhimurium: Mutagenicidade e antimutagenicidade
dc.typeArtigo


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