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dc.contributor.authorRobledo Restrepo, Sara María-
dc.contributor.authorCardona Galeano, Wilson-
dc.contributor.authorLigardo Restrepo, Karen Patricia-
dc.contributor.authorHenao Peláez, Jéssica Natalia-
dc.contributor.authorArbeláez Córdoba, Natalia-
dc.contributor.authorMontoya Cuervo, Edwin Andrés-
dc.contributor.authorAlzate Guarín, Fernando-
dc.contributor.authorPérez Cardona, Juan Manuel-
dc.contributor.authorArango Valencia, Víctor Hugo-
dc.contributor.authorVélez Bernal, Iván Darío-
dc.contributor.authorSáez Vega, Jairo Antonio-
dc.date.accessioned2021-09-03T02:17:55Z-
dc.date.available2021-09-03T02:17:55Z-
dc.date.issued2015-
dc.identifier.citationRobledo, S., Cardona, W., Ligardo, K., Henao, H., Arbeláez, N., Montoya, A., Alzate, F., Pérez, J., Arango, V., Vélez, I., Sáez, J. (2015). Antileishmanial Effect of 5,3′-Hydroxy-7,4′-dimethoxyflavanone of Picramnia gracilis Tul. (Picramniaceae) Fruit: In Vitro and In Vivo Studies. Advances in Pharmacological and Pharmaceutical Sciences, vol. 2015, 1-8. https://doi.org/10.1155/2015/978379spa
dc.identifier.issn1687-6334-
dc.identifier.urihttp://hdl.handle.net/10495/22106-
dc.description.abstractABSTRACT: Species of Picramnia genus are used in folk medicine to treat or prevent skin disorders, but only few species have been studied for biological activity and chemical composition. P. gracilis Tul. is a native species from Central and South America and although its fruits are edible, phytochemical analysis or medicinal uses of this species are not known. In the search of candidates to antileishmanial drugs, this work aimed to evaluate the antileishmanial activity of P. gracilis Tul. in in vitro and in vivo studies. Only ethanolic extract of fruits showed leishmanicidal activity. The majoritarian metabolite was 5,3′-hydroxy-7,4′-dimethoxyflavanone ether that exhibited high activity against L. (V.) panamensis (EC50 17.0 + 2.8 mg/mL, 53.7 μM) and low toxicity on mammalian U-937 cells, with an index of selectivity >11.8. In vivo studies showed that the flavanone administered in solution (2 mg/kg/day) or cream (2%) induces clinical improvement and no toxicity in hamsters with CL. In conclusion, this is the first report about isolation of 5,3′-hydroxy-7,4′-dimethoxyflavanone of P. gracilis Tul. The leishmanicidal activity attributed to this flavanone is also reported for the first time. Finally, the in vitro and in vivo leishmanicidal activity reported here for 5,3′-hydroxy-7,4′-dimethoxyflavanone offers a greater prospect towards antileishmanial drug discovery and development.spa
dc.format.extent8spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherHindawispa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleAntileishmanial Effect of 5,3´ -Hydroxy-7,4´ -dimethoxyflavanone of Picramnia gracilis Tul. (Picramniaceae) Fruit: In Vitro and In Vivo Studiesspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGrupo de Estudios Botánicosspa
dc.publisher.groupPrograma de Estudio y Control de Enfermedades Tropicales (PECET)spa
dc.publisher.groupQuímica de Plantas Colombianasspa
dc.identifier.doi10.1155/2015/978379-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1687-6342-
oaire.citationtitleAdvances in Pharmacological Sciencesspa
oaire.citationstartpage1spa
oaire.citationendpage8spa
oaire.citationvolume2015spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.publisher.placeLondres, Inglaterraspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsEnfermedades de la Piel-
dc.subject.decsSkin Diseases-
dc.subject.decsLeishmaniasis-
dc.subject.agrovocComposición química-
dc.subject.agrovocChemical composition-
dc.subject.proposalPicramniaspa
dc.subject.proposalActividad biológica-
dc.subject.proposalAntileishmanialspa
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_1794-
dc.description.researchgroupidCOL0015099spa
dc.description.researchgroupidCOL0015329spa
dc.description.researchgroupidCOL0008227spa
dc.relation.ispartofjournalabbrevAdv. Pharmacol. Sci.spa
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