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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/131539
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dc.contributor.authorArwa, Phanuel Saroni-
dc.contributor.authorZeraik, Maria Luiza-
dc.contributor.authorFarias Ximenes, Valdecir-
dc.contributor.authorFonseca, Luiz Marcos da-
dc.contributor.authorBolzani, Vanderlan da Silva-
dc.contributor.authorSiqueira Silva, Dulce Helena-
dc.date.accessioned2015-12-07T15:37:13Z-
dc.date.accessioned2016-10-25T21:23:46Z-
dc.date.available2015-12-07T15:37:13Z-
dc.date.available2016-10-25T21:23:46Z-
dc.date.issued2015-08-27-
dc.identifierhttp://dx.doi.org/10.1016/j.jep.2015.08.041-
dc.identifier.citationJournal Of Ethnopharmacology, v. 174, p. 410-418, 2015.-
dc.identifier.issn1872-7573-
dc.identifier.urihttp://hdl.handle.net/11449/131539-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/131539-
dc.description.abstractGarcinia brasiliensis, a plant native to the Brazilian Amazon Rainforest, is used in traditional medicine to treat inflammation of the urinary tract, peptic ulcers, arthritis and other conditions. The purposes of this study were to analyze the chemical constituents of G. brasiliensis branches and leaves and to evaluate the potential of isolated compounds to act as inhibitors of both the oxidative burst of stimulated neutrophils and oxidative damage in human erythrocyte membranes to verify the antioxidant and anti-inflammatory effects of this plant. Neutrophils were isolated from the blood of healthy donors by Ficoll-Paque density gradient centrifugation. Superoxide anion and total reactive oxygen species (ROS) produced by stimulated neutrophils were measured by WST-1 reduction and luminol-enhanced chemiluminescence assays, respectively. Radical-induced lipoperoxidation and hemolysis were performed using erythrocytes from the blood of healthy donors. Compounds were isolated from G. brasiliensis branches and leaves by HPLC microfractionation, and structure elucidation of the isolated compounds was performed based on NMR and HR-MS analyses. The biflavonoids procyanidin, fukugetin, amentoflavone and podocarpusflavone isolated from G. brasiliensis showed potent inhibitory effects on the oxidative burst of human neutrophils, inhibiting ROS production by 50% at 1 μmol L(-1). These biflavonoids also proved to be potent inhibitors of hemolysis (with 88±7% inhibition at 50 µmol L(-1) for procyanidin) and lipid peroxidation in human erythrocytes, with a malondialdehyde level (a biomarker of oxidative stress) of 8.5±0.3nmol/mg Hb at 50µmol L(-1) for procyanidin. These findings indicate that the biflavonoids extracted from G. brasiliensis branches and leaves modulate oxidative stress via inhibition of NADPH oxidase and ROS production by stimulated human neutrophils. Furthermore, the biflavonoids exhibited potent inhibition of oxidant hemolysis and lipid peroxidation induced by AAPH in human erythrocytes. Therefore, these studies suggest the use of G. brasiliensis extract as an antioxidant and anti-inflammatory agent.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent410-418-
dc.language.isoeng-
dc.publisherElsevier B. V.-
dc.sourcePubMed-
dc.subjectAnti-inflammatoryen
dc.subjectAntioxidanten
dc.subjectBiflavonoidsen
dc.subjectErythrocytesen
dc.subjectGarcinia brasiliensisen
dc.subjectNeutrophilsen
dc.titleRedox-active biflavonoids from Garcinia brasiliensis as inhibitors of neutrophil oxidative burst and human erythrocyte membrane damageen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Organic Chemistry, Nucleus of Bioassays, Ecophysiology and Biosynthesis of Natural Products (NUBBE), Institute of Chemistry, São Paulo State University (UNESP), P. O. Box 355, 14800-900, Araraquara, São Paulo, Brazil.-
dc.description.affiliationDepartment of Organic Chemistry, Nucleus of Bioassays, Ecophysiology and Biosynthesis of Natural Products (NUBBE), Institute of Chemistry, São Paulo State University (UNESP), P. O. Box 355, 14800-900, Araraquara, São Paulo, Brazil. Electronic address: marialuizaze@gmail.com.-
dc.description.affiliationDepartment of Chemistry, School of Sciences, São Paulo State University (UNESP), P. O. Box 473, 17033-360, Bauru, São Paulo, Brazil.-
dc.description.affiliationDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (UNESP), P. O. Box 502, 14801-902, Araraquara, São Paulo, Brazil.-
dc.description.affiliationDepartment of Organic Chemistry, Nucleus of Bioassays, Ecophysiology and Biosynthesis of Natural Products (NUBBE), Institute of Chemistry, São Paulo State University (UNESP), P. O. Box 355, 14800-900, Araraquara, São Paulo, Brazil.-
dc.description.affiliationUnespDepartment of Organic Chemistry, Nucleus of Bioassays, Ecophysiology and Biosynthesis of Natural Products (NUBBE), Institute of Chemistry, São Paulo State University (UNESP), P. O. Box 355, 14800-900, Araraquara, São Paulo, Brazil.-
dc.description.affiliationUnespDepartment of Organic Chemistry, Nucleus of Bioassays, Ecophysiology and Biosynthesis of Natural Products (NUBBE), Institute of Chemistry, São Paulo State University (UNESP), P. O. Box 355, 14800-900, Araraquara, São Paulo, Brazil. Electronic address: marialuizaze@gmail.com.-
dc.description.affiliationUnespDepartment of Chemistry, School of Sciences, São Paulo State University (UNESP), P. O. Box 473, 17033-360, Bauru, São Paulo, Brazil.-
dc.description.affiliationUnespDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (UNESP), P. O. Box 502, 14801-902, Araraquara, São Paulo, Brazil.-
dc.description.affiliationUnespDepartment of Organic Chemistry, Nucleus of Bioassays, Ecophysiology and Biosynthesis of Natural Products (NUBBE), Institute of Chemistry, São Paulo State University (UNESP), P. O. Box 355, 14800-900, Araraquara, São Paulo, Brazil.-
dc.description.sponsorshipIdFAPESP: 2010/52327-5-
dc.description.sponsorshipIdFAPESP: 2013/07600-3-
dc.description.sponsorshipIdFAPESP: 2011/03017-6-
dc.identifier.doi10.1016/j.jep.2015.08.041-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal Of Ethnopharmacology-
dc.identifier.pubmed26320685-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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