Please use this identifier to cite or link to this item: http://www.repositorio.ufc.br/handle/riufc/26602
Title in Portuguese: Chronic treatment with zoledronic acid increases inflammatory markers in periodontium of rats
Author: Silva, Paulo Goberlânio de Barros
Ferreira Junior, Antonio Ernando Carlos
Oliveira, Camila Carvalho de Oliveira
Brizeno, Luiz André Cavalcante
Wong, Deysi Viviana Tenazoa
Lima Júnior, Roberto César Pereira
Sousa, Fabrício Bitú
Mota, Mário Rogério Lima
Alves, Ana Paula Negreiros Nunes
Keywords: Difosfonatos
Diphosphonates
Estresse Oxidativo
Issue Date: Aug-2017
Publisher: Journal of Oral Pathology and Medicine
Citation: SILVA, P. G. B. et al. Chronic treatment with zoledronic acid increases inflammatory markers in periodontium of rats. Journal of Oral Pathology and Medicine, Copenhagen, p. 1-8, aug. 2017.
Abstract: Background: Bisphosphonates (BF) rise proinflammatory markers and irreversibly bind to bone. Chronically, BF can lead to an inflammatory status and can increase the local oxidative stress in periodontium. Therefore, the objective of this study was to evaluate whether the chronic infusion of Zoledronic Acid (ZA) increases inflam- matory markers in periodontium of rats. Methods and results: Chronically, infusion therapy was performed with ZA (0.04, 0.2 or 1 mg/kg or saline) by four doses in over a 70-day period to analyze periodontium of the first right inferior molar using histologic, histochemical (toluidine blue), and immunohistochemical (CD68, tumor necrosis factor- a (TNF-a), interleukin-1beta (IL- 1b), inducible nitric oxide synthase (iNOS) and nuclear factor kappa B (NF-kB)) tests. The experiment was replicated (ZA 0.2 mg/kg versus saline) for myeloperoxidase (MPO) assay and dose TNF-a, IL-1b, malondialdehyde (MDA) and glutathione (GSH) in gingiva of the same tooth. Despite there is no alteration in mast cells (P = .608) and CD68 mononuclear-positive cells (P = .351), in the periodontium of the ZA-treated group, was observed an increase in the presence of inflammatory cells (P = .001) and cytoplasmic immunostaining for TNF-a (P = .003), IL-1b (P = .004), iNOS (P = .008), and NF-kB (P = .025). Levels of MPO (P < .001), TNF-a (P = .002), IL-1b (P < .001), and GSH (P = .005) were augmented in gingiva of ZA-treated group but MDA (P = .993) levels and NF-kB nuclear staining (P = .923) were not altered. Conclusions: Chronic treatment with ZA increase proinflammatory cytokines and the number of inflammatory cells in periodontium of rats and GSH are expressed probably in a compensatory manner.
URI: http://www.repositorio.ufc.br/handle/riufc/26602
ISSN: 0904-2512
1600-0714
Appears in Collections:DFAR - Artigos publicados em revistas científicas

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