Please use this identifier to cite or link to this item: http://repositorio.unitau.br/jspui/handle/20.500.11874/2986
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dc.contributor.authorCastro, Myrella L.pt_BR
dc.contributor.authorFranco, Gilson Cesar Nobrept_BR
dc.contributor.authorBranco-de-Almeida, Luciana S.pt_BR
dc.contributor.authorAnbinder, Ana Liapt_BR
dc.contributor.authorCogo-Mueller, Karinapt_BR
dc.contributor.authorCortelli, Sheila Cavalcapt_BR
dc.contributor.authorDuarte, Simonept_BR
dc.contributor.authorSaxena, Deepakpt_BR
dc.contributor.authorRosalen, Pedro L.pt_BR
dc.date.accessioned2019-09-12T16:56:59Z-
dc.date.available2019-09-12T16:56:59Z-
dc.date.issued2016-
dc.citation.volume87pt_BR
dc.citation.issue2pt_BR
dc.citation.spage203-
dc.citation.epage210-
dc.identifier.doi10.1902/jop.2015.150385pt_BR
dc.identifier.issn0022-3492-
dc.identifier.issn1943-3670-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/2986-
dc.description.abstractBackground: Subantimicrobial dose doxycycline (SDD) has been used as an adjunct in periodontal treatment because of its matrix metalloproteinase inhibition properties. Although the benefits of SDD therapy, such as improvement in the parameters of periodontal probing depth and clinical attachment level, have been proven in multiple clinical studies, the comprehension of other biologic mechanisms of action on periodontitis remains poorly investigated. Therefore, this animal-model study evaluated the effects of SDD monotherapy on the expressions of the following key proinflammatory genes: proteinase-activated receptor-2 (PAR(2)), tumor necrosis factor (TNF)-alpha, interleukin (IL)-17, and IL-1 beta. Methods: Male Wistar rats were assigned randomly to the following: 1) control group: no ligature-induced periodontitis and no treatment; 2) ligature group: ligature-induced periodontitis and placebo treatment; and 3) ligature + doxycycline group: ligature-induced periodontitis and SDD treatment. After the experimental time, animals were sacrificed, and reverse transcription-polymerase chain reaction was performed to analyze the mRNA expression of IL-1 beta, IL-17, TNF-alpha, and PAR(2) in gingival tissue samples. Histologic analyses were performed on the furcation region and mesial gingiva of mandibular first molars to measure periodontal bone loss and collagen content. Results: SDD administration significantly downregulated PAR(2), IL-17, TNF-alpha, and IL-1 beta mRNA expressions (P < 0.05). In addition, SDD treatment was accompanied by lower rates of alveolar bone loss (P < 0.05) and maintenance of the amount of gingival collagen fibers. Conclusion: These findings reveal new perspectives regarding SDD efficacy because it can be partially related to proinflammatory gene expression modulation, even considering PAR(2) and IL-17, which has not been investigated thus far.en
dc.description.provenanceMade available in DSpace on 2019-09-12T16:56:59Z (GMT). No. of bitstreams: 0 Previous issue date: 2016en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt_BR
dc.languageInglêspt_BR
dc.publisherWiley-
dc.publisher.countryEstados Unidospt_BR
dc.relation.ispartofJournal of Periodontology-
dc.rightsEm verificaçãopt_BR
dc.sourceWeb of Sciencept_BR
dc.subject.otherAlveolar Bone Lossen
dc.subject.otherDoxycyclineen
dc.subject.otherPeriodontal Diseasesen
dc.subject.otherReceptor, Par-2en
dc.subject.otherPorphyromonas-Gingivalisen
dc.subject.otherBone Lossen
dc.subject.otherMatrix Metalloproteinasesen
dc.subject.otherAdult Periodontitisen
dc.subject.otherExpressionen
dc.subject.otherDiseaseen
dc.subject.otherCytokinesen
dc.subject.otherIl-17en
dc.subject.otherMatrix-Metalloproteinase-9en
dc.subject.otherPathogenesisen
dc.titleDownregulation of Proteinase-Activated Receptor-2, Interleukin-17, and Other Proinflammatory Genes by Subantimicrobial Doxycycline Dose in a Rat Periodontitis Modelen
dc.typeArtigo de Periódicopt_BR
dc.contributor.orcidMuller, Karina Cogo https://orcid.org/0000-0002-9048-8702pt_BR
dc.contributor.orcidRosalen, Pedro Luiz https://orcid.org/0000-0003-0812-4027pt_BR
dc.contributor.orcidBranco-de-Almeida, Luciana https://orcid.org/0000-0001-6928-8522pt_BR
dc.contributor.orcidAnbinder, Ana Lia https://orcid.org/0000-0003-3930-4274pt_BR
dc.contributor.researcheridMuller, Karina Cogo/H-2365-2012pt_BR
dc.contributor.researcheridRosalen, Pedro Luiz/I-3718-2012pt_BR
dc.contributor.researcheridSaxena, Deepak/K-1864-2019pt_BR
dc.identifier.wosWOS:000369132500016-
dc.description.affiliation[Castro, Myrella L.; Rosalen, Pedro L.] Univ Estadual Campinas, Piracicaba Dent Sch, Dept Physiol Sci, Ave Limeira 901,Caixa Postal 52, BR-13414903 Sao Paulo, Brazil-
dc.description.affiliation[Franco, Gilson C. N.] Univ Estadual Ponta Grossa, Dept Gen Biol, Ponta Grossa, Parana, Brazil-
dc.description.affiliation[Branco-de-Almeida, Luciana S.] Univ Fed Maranhao, Dept Dent 2, Sao Luis, Maranhao, Brazil-
dc.description.affiliation[Anbinder, Ana L.] Univ Estadual Paulista, Inst Sci & Technol Sao Jose dos Campos, Dept Biosci & Oral Diag, Sao Paulo, SP, Brazil-
dc.description.affiliation[Cogo-Mueller, Karina] Univ Santo Amaro, Dept Dent, Implantol Area, Sao Paulo, SP, Brazil-
dc.description.affiliation[Cortelli, Sheila C.] Universidade de Taubaté (Unitau), Nucleus Periodontal Res, Sao Paulo, Brazil-
dc.description.affiliation[Duarte, Simone; Saxena, Deepak] NYU, Coll Dent, Dept Basic Sci & Craniofacial Biol, New York, NY USA-
dc.subject.wosareaDentistry, Oral Surgery & Medicineen
dc.subject.researchareaDentistry, Oral Surgery & Medicineen
Appears in Collections:Artigos de Periódicos

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