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Exogenous Administration of 15d-PGJ(2)-Loaded Nanocapsules Inhibits Bone Resorption in a Mouse Periodontitis Model

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. [UNESP]
dc.contributor.authorFraceto, Leonardo F. [UNESP]
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.date.accessioned2014-05-20T13:12:11Z
dc.date.available2014-05-20T13:12:11Z
dc.date.issued2012-07-15
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.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.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 10/15014-9
dc.description.sponsorshipIdCNPq: 471305/2009-0
dc.format.extent1043-1052
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.doi10.4049/jimmunol.1200730
dc.identifier.issn0022-1767
dc.identifier.urihttp://hdl.handle.net/11449/174
dc.identifier.wosWOS:000306119800062
dc.language.isoeng
dc.publisherAmer Assoc Immunologists
dc.relation.ispartofJournal of Immunology
dc.relation.ispartofjcr4.539
dc.relation.ispartofsjr2,837
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.titleExogenous Administration of 15d-PGJ(2)-Loaded Nanocapsules Inhibits Bone Resorption in a Mouse Periodontitis Modelen
dc.typeArtigo
dcterms.licensehttp://www.jimmunol.org/site/misc/authorinstructions.xhtml#copyright
dcterms.rightsHolderAmer Assoc Immunologists
dspace.entity.typePublication
unesp.author.orcid0000-0003-4472-365X[1]
unesp.author.orcid0000-0002-5669-4190[2]
unesp.author.orcid0000-0003-0765-4421[6]
unesp.author.orcid0000-0002-2827-2038[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, Sorocabapt
unesp.departmentEngenharia Ambiental - ICTSpt

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