Produção de IL-1β, IL-6 e IL-8 por fibroblastos estimulados por cimentos endodônticos e submetidos à terapia laser de baixa potência

• Ano de defesa: 2015
• Autor(a) principal: Miranda, Rosana Belchior
• Orientador(a): Fidel, Sandra Rivera
• Banca de defesa: Freitas, Lilian Ferreira , Pinho, Marco André de Berrêdo , Bruno, Adilia Maria Vieira , Ferreira, Leila Soares , Fidel, Rivail Antonio Sergio
• Tipo de documento: Tese
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade do Estado do Rio de Janeiro
• Programa de Pós-Graduação: Programa de Pós-Graduação em Odontologia
• Departamento: Centro Biomédico::Faculdade de Odontologia
• País: BR
• Palavras-chave em Português: Cimentos endodônticos; Cultura celular; Citocinas; Terapia laser de baixa potência
• Palavras-chave em Inglês: Endodontic cements; Cell culture; Cytokines; Low-level laser therapy
• Área do conhecimento CNPq: CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA::ENDODONTIA
• Link de acesso: http://www.bdtd.uerj.br/handle/1/14033

Endodontic treatment success depends on careful accomplishment of all steps, finishing with a three-dimensional obturation that reachs the entire root canal system. Thus, the obturation materials or the substances that are released will be in contact with perirradicular tissues, which may influence the inflammatory response and the repair process. Low-level laser therapy (LLLT) has been studied about its anti-inflammatory action, improving the repair. The aim of this study was to investigate the production of IL-1β, IL-6 and IL-8 cytokines by human gingival fibroblasts (FMM1 lineage) as a response to the extracts of the endodontic cements AH Plus, MTA Fillapex and EndoSequence BC Sealer, besides the effectiveness of LLLT in this model. For that, freshly mixed and 24 h-set elutes of these sealers were prepared, in fresh DMEM, in accordance with ISO 10993-12. Firstly, cytotoxicity was assessed after cells were treated with cements extracts serial dilution (1:1 to 1:16), by MTT assay. To evaluate the cytokines production, 106 cells per well were cultured at 24-well-plates to interact with the 1:4 dilution of sealers extracts. Non-irradiated and irradiated groups were established. On the irradiated group, the cell culture received two InGaAlP laser irradiation (660 nm, 30 mW, 5 J/cm2, 0.028 cm2 spot size) at 12h-interval. The non-irradiated group was submitted to the same environment conditions of the irradiated group. The culture supernatants were collected, centrifuged, aliquoted and stored frozen to further analyse by ELISA assay. Data obtained (media ± standard error) were treated by ANOVA one-way, complemented by Tuckey s test and ANOVA two-way, with Bonferroni correction (p< 0.05). The cytotoxicity of AH Plus and EndoSequence BC Sealer was related to time/dose-dependent manner, whilst MTA Fillapex cytotoxicity was showed as dose-dependent manner. The endodontic sealers inducted the production of IL-1β, IL-6 and IL-8 cytokines by fibroblasts similar to control (p> 0.05). Only E. coli LPS was capable to stimulate IL-8 secretion with statistic difference (p< 0.05). TLBP was not able to modulate the secretion of these cytokines, significantly.