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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/174
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dc.contributor.authorNapimoga, Marcelo H.-
dc.contributor.authorda Silva, Carlos A. T.-
dc.contributor.authorCarregaro, Vanessa-
dc.contributor.authorFarnesi-de-Assuncao, Thais S.-
dc.contributor.authorDuarte, Poliana M.-
dc.contributor.authorde Melo, Nathalie F. S.-
dc.contributor.authorFraceto, Leonardo F.-
dc.date.accessioned2014-05-20T13:12:11Z-
dc.date.accessioned2016-10-25T16:32:32Z-
dc.date.available2014-05-20T13:12:11Z-
dc.date.available2016-10-25T16:32:32Z-
dc.date.issued2012-07-15-
dc.identifierhttp://dx.doi.org/10.4049/jimmunol.1200730-
dc.identifier.citationJournal of Immunology. Bethesda: Amer Assoc Immunologists, v. 189, n. 2, p. 1043-1052, 2012.-
dc.identifier.issn0022-1767-
dc.identifier.urihttp://hdl.handle.net/11449/174-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/174-
dc.description.abstractThe 15-deoxy-(Delta 12,14)-PG J(2) (15d-PGJ(2)) has demonstrated excellent anti-inflammatory results in different experimental models. It can be used with a polymeric nanostructure system for modified drug release, which can change the therapeutic properties of the active principle, leading to increased stability and slower/prolonged release. The aim of the current study was to test a nano-technological formulation as a carrier for 15d-PGJ(2), and to investigate the immunomodulatory effects of this formulation in a mouse periodontitis model. Poly (D, L-lactide-coglycolide) nanocapsules (NC) were used to encapsulate 15d-PGJ(2). BALB/c mice were infected on days 0, 2, and 4 with Aggregatibacter actinomycetemcomitans and divided into groups (n = 5) that were treated daily during 15 d with 1, 3, or 10 mu g/kg 15d-PGJ(2)-NC. The animals were sacrificed, the submandibular lymph nodes were removed for FACS analysis, and the jaws were analyzed for bone resorption by morphometry. Immunoinflammatory markers in the gingival tissue were analyzed by reverse transcriptase-quantitative PCR, Western blotting, or ELISA. Infected animals treated with the 15d-PGJ(2)-NC presented lower bone resorption than infected animals without treatment (p < 0.05). Furthermore, infected animals treated with 10 mu g/kg 15d-PGJ(2)-NC had a reduction of CD4(+)CD25(+)FOXP3(+) cells and CD4/CD8 ratio in the submandibular lymph node (p < 0.05). Moreover, CD55 was upregulated, whereas RANKL was downregulated in the gingival tissue of the 10 mu g/kg treated group (p < 0.05). Several proinflammatory cytokines were decreased in the group treated with 10 mu g/kg 15d-PGJ(2)-NC, and high amounts of 15d-PGJ(2) were observed in the gingiva. In conclusion, the 15d-PGJ(2)-NC formulation presented immunomodulatory effects, decreasing bone resorption and inflammatory responses in a periodontitis mouse model. The Journal of Immunology, 2012, 189: 1043-1052.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.format.extent1043-1052-
dc.language.isoeng-
dc.publisherAmer Assoc Immunologists-
dc.sourceWeb of Science-
dc.titleExogenous Administration of 15d-PGJ(2)-Loaded Nanocapsules Inhibits Bone Resorption in a Mouse Periodontitis Modelen
dc.typeoutro-
dc.contributor.institutionSao Leopoldo Mandic Inst & Res Ctr-
dc.contributor.institutionUniversidade Federal do Triângulo Mineiro (UFTM)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniv Guarulhos-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationSao Leopoldo Mandic Inst & Res Ctr, Lab Immunol & Mol Biol, BR-13045755 Campinas, SP, Brazil-
dc.description.affiliationUniv Fed Triangulo Mineiro, Immunol Lab, BR-38025180 Uberaba, MG, Brazil-
dc.description.affiliationUniv São Paulo, Fac Med Ribeirao Preto, Dept Immunol, BR-14049900 Ribeirao Preto, SP, Brazil-
dc.description.affiliationUniv Guarulhos, Dept Periodont, Dent Res Div, BR-07023070 São Paulo, Brazil-
dc.description.affiliationUniv Estadual Campinas, Dept Biochem, BR-13083970 Campinas, SP, Brazil-
dc.description.affiliationSão Paulo State Univ, Dept Environm Engn, BR-18087180 Sorocaba, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Dept Environm Engn, BR-18087180 Sorocaba, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 10/15014-9-
dc.description.sponsorshipIdCNPq: 471305/2009-0-
dc.identifier.doi10.4049/jimmunol.1200730-
dc.identifier.wosWOS:000306119800062-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Immunology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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