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dc.contributor.authorDomingues, Alexandre-
dc.contributor.authorSartori, Alexandrina-
dc.contributor.authorGolim, Márjorie de Assis-
dc.contributor.authorMarino Valente, Ligia Maria-
dc.contributor.authorda Rosa, Larissa Camargo-
dc.contributor.authorWatanabe Ishikawa, Larissa Lumi-
dc.contributor.authorSiani, Antonio Carlos-
dc.contributor.authorViero, Rosa Marlene-
dc.date.accessioned2014-05-20T13:51:14Z-
dc.date.available2014-05-20T13:51:14Z-
dc.date.issued2011-09-01-
dc.identifierhttp://dx.doi.org/10.1016/j.jep.2011.06.021-
dc.identifier.citationJournal of Ethnopharmacology. Clare: Elsevier B.V., v. 137, n. 1, p. 635-642, 2011.-
dc.identifier.issn0378-8741-
dc.identifier.urihttp://hdl.handle.net/11449/18288-
dc.description.abstractEthnopharmacological relevance: Uncaria tomentosa (Willd.) DC (Rubiaceae) is a species native to the Amazon rainforest and surrounding tropical areas that is endowed with immunomodulatory properties and widely used around the world. In this study we investigated the immunomodulatory potential of Uncaria tomentosa (UT) aqueous-ethanol extract on the progression of immune-mediated diabetes.Materials and methods: C57BL/6 male mice were injected with MLDS (40 mg/kg) and orally treated with UT at 10-400 mg/kg during 21 days. Control groups received MLDS alone or the respective dilution vehicle. Pancreatic mononuclear infiltrate and beta-cell insulin content were analyzed by HE and immunohistochemical staining, respectively, and measured by digital morphometry. Lymphocyte immunophenotyping and cytokine production were determined by flow cytometry analysis.Results: Treating the animals with 50-400 mg/kg of UT caused a significant reduction in the glycemic levels, as well as in the incidence of diabetes. The morphometric analysis of insulitis revealed a clear protective effect. Animals treated with UT at 400 mg/kg presented a higher number of intact islets and a significant inhibition of destructive insulitis. Furthermore, a significant protection against the loss of insulin-secreting presented beta-cells was achieved, as observed by a careful immunohistochemical evaluation. The phenotypic analysis indicated that the groups treated with higher doses (100-400 mg/kg) presented CD4(+) and CD8(+) T-cell values similar to those observed in healthy animals. These same higher doses also increased the number of CD4(+)CD25(+)Foxp3(+) regulatory T-cells. Moreover, the extract modulated the production of Th1 and Th2, with increased levels of IL-4 and IL-5.Conclusions: The extract was effective to prevent the progression of immune-mediated diabetes by distinct pathways. (C) 2011 Elsevier B.V. All rights reserved.en
dc.format.extent635-642-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectUncaria tomentosaen
dc.subjectDiabetesen
dc.subjectRegulatory T cellsen
dc.subjectCytokineen
dc.subjectStreptozotocinen
dc.titlePrevention of experimental diabetes by Uncaria tomentosa extract: Th2 polarization, regulatory T cell preservation or both?en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal do Rio de Janeiro (UFRJ)-
dc.contributor.institutionOswaldo Cruz Fdn FIOCRUZ-
dc.description.affiliationSão Paulo State Univ UNESP, Sch Med, Dept Pathol, BR-18618000 São Paulo, Brazil-
dc.description.affiliationSão Paulo State Univ UNESP, Dept Microbiol & Immunol, Biosci Inst, BR-18618000 São Paulo, Brazil-
dc.description.affiliationSão Paulo State Univ UNESP, Sch Med, Ctr Hematol, BR-18618000 São Paulo, Brazil-
dc.description.affiliationUniv Fed Rio de Janeiro, Inst Chem, Dept Organ Chem, BR-21941909 Rio de Janeiro, Brazil-
dc.description.affiliationOswaldo Cruz Fdn FIOCRUZ, Dept Nat Prod, Inst Pharmaceut Technol, BR-21041250 Rio de Janeiro, Brazil-
dc.description.affiliationUnespSão Paulo State Univ UNESP, Sch Med, Dept Pathol, BR-18618000 São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ UNESP, Dept Microbiol & Immunol, Biosci Inst, BR-18618000 São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ UNESP, Sch Med, Ctr Hematol, BR-18618000 São Paulo, Brazil-
dc.identifier.doi10.1016/j.jep.2011.06.021-
dc.identifier.wosWOS:000295236700075-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000295236700075.pdf-
dc.relation.ispartofJournal of Ethnopharmacology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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