You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/15906
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGuimaraes, M. R.-
dc.contributor.authorCoimbra, L. S.-
dc.contributor.authorde Aquino, S. G.-
dc.contributor.authorSpolidório, Luis Carlos-
dc.contributor.authorKirkwood, K. L.-
dc.contributor.authorRossa, C.-
dc.date.accessioned2013-09-30T18:32:25Z-
dc.date.accessioned2014-05-20T13:45:15Z-
dc.date.accessioned2016-10-25T16:59:17Z-
dc.date.available2013-09-30T18:32:25Z-
dc.date.available2014-05-20T13:45:15Z-
dc.date.available2016-10-25T16:59:17Z-
dc.date.issued2011-04-01-
dc.identifierhttp://dx.doi.org/10.1111/j.1600-0765.2010.01342.x-
dc.identifier.citationJournal of Periodontal Research. Malden: Wiley-blackwell, v. 46, n. 2, p. 269-279, 2011.-
dc.identifier.issn0022-3484-
dc.identifier.urihttp://hdl.handle.net/11449/15906-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/15906-
dc.description.abstractBackground and Objective:Curcumin is a plant-derived dietary spice with various biological activities, including anticarcinogenic and anti-inflammatory effects. Its therapeutic applications have been studied in a variety of conditions, including rheumatoid arthritis, colon cancer and depression, but no studies have evaluated the effects of curcumin on periodontal disease in vivo.Material and Methods:Experimental periodontal disease was induced in rats by placing cotton ligatures around both lower first molars. Curcumin was given to the rats by the intragastric route daily at two dosages (30 and 100 mg/kg) for 15 d. Control animals received ligatures but only the corn oil vehicle by gavage, and no treatment-negative control animals were included. Bone resorption was assessed by micro-computed tomography, and the inflammatory status was evaluated by stereometric analysis. Both RT-qPCR and ELISA were used to determine the expression of interleukin-6, tumor necrosis factor-alpha and prostaglandin E(2) synthase in the gingival tissues. Modulation of p38 MAPK and nuclear factor-kappa B activation were assessed by western blotting.Results:Bone resorption was effectively induced in the experimental period, but it was not affected by either dose of curcumin. Curcumin effectively inhibited cytokine gene expression at both the mRNA and the protein level and produced a dose-dependent inhibition of the activation of nuclear factor-kappa B in the gingival tissues. Activation of p38 MAPK was not inhibited by curcumin. Curcumin-treated animals also presented a marked reduction of the inflammatory cell infiltrate and increased collagen content and fibroblastic cell numbers.Conclusion:Curcumin did not prevent alveolar bone resorption, but its potent anti-inflammatory effect suggests that it may have a therapeutic potential in periodontal diseases.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.description.sponsorshipNational Institutes of Health - National Institute of Dental and Craniofacial Research-
dc.description.sponsorshipNational Center for Research Resources-
dc.format.extent269-279-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.sourceWeb of Science-
dc.subjectcurcuminen
dc.subjectinflammationen
dc.subjectperiodontal diseaseen
dc.subjectnuclear factor-kappa Ben
dc.subjectp38 mitogen-activated protein kinaseen
dc.titlePotent anti-inflammatory effects of systemically administered curcumin modulate periodontal disease in vivoen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionMed Univ S Carolina-
dc.description.affiliationUniv Estadual Paulista UNESP, Dept Diag, Fac Odontol Araraquara, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista UNESP, Dept Surg, Fac Odontol Araraquara, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista UNESP, Dept Physiol, Fac Odontol Araraquara, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista UNESP, Dept Pathol, Fac Odontol Araraquara, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationMed Univ S Carolina, Dept Craniofacial Biol, Charleston, SC 29425 USA-
dc.description.affiliationMed Univ S Carolina, Coll Dent Med, Ctr Oral Hlth Res, Charleston, SC 29425 USA-
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Dept Diag, Fac Odontol Araraquara, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Dept Surg, Fac Odontol Araraquara, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Dept Physiol, Fac Odontol Araraquara, BR-14801903 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Dept Pathol, Fac Odontol Araraquara, BR-14801903 Araraquara, SP, Brazil-
dc.description.sponsorshipIdCAPES: 4638-05-
dc.description.sponsorshipIdNIH/NIDCR: 1R01DE018290-
dc.description.sponsorshipIdNational Center for Research Resources: P20RR017696-
dc.identifier.doi10.1111/j.1600-0765.2010.01342.x-
dc.identifier.wosWOS:000287702700017-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Periodontal Research-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.