Artículos de revistas
Multiple Apical Periodontitis Influences Serum Levels of Cytokines and Nitric Oxide
Fecha
2016-05-01Registro en:
Journal Of Endodontics. New York: Elsevier Science Inc, v. 42, n. 5, p. 747-751, 2016.
0099-2399
10.1016/j.joen.2016.01.022
WOS:000375512900011
WOS000375512900011.pdf
4408095517346846
0000-0003-4859-0583
Autor
Universidade Estadual Paulista (Unesp)
Institución
Resumen
In(t)roduction: This study evaluated whether apical periodontitis (AP) in a single tooth or in multiple teeth affected serum levels of inflammatory mediators and influenced blood homeostasis. Methods: Thirty male Wistar rats were divided into 3 groups of 10 rats each: control group, healthy rats; 1AP group, rats with AP in 1 tooth; and 4AP group, rats with AP in 4 teeth. After 30 days, the rats were anesthetized, and their blood was collected through cardiac puncture to quantify tumor necrosis factor alpha (TNF-alpha), interferon gamma (IFN-gamma), interleukin (IL)-6, IL-17, IL-23, and nitric oxide (NO) levels. The rats were then sacrificed by administering an anesthetic overdose. Their maxillary and mandibular molars were collected and processed for histologic analysis with hematoxylineosin and for immunohistochemical staining of the cytokines and NO-producing enzyme nitric oxide synthase. Results of these analyses were statistically analyzed; P < .05 was considered statistically significant. Results: Rats in the 1AP and 4AP groups showed increased IL-6, IL-17, IL-23, TNF-alpha, IFN-gamma, and NO synthase expression; inflammatory cell infiltration; and moderate bone resorption in affected teeth. Serum TNF-alpha, IL-6, IL-17, and IL-23 levels were higher in rats in the 4AP group than in those in the control group (P < .05). Serum NO levels were significantly lower in rats in the 1AP and 4AP groups than in those in the control group (P < .05). Serum IFN-gamma levels were not different-among rats in the 3 groups (P > .05). Conclusions: These results suggested that AP affected blood homeostasis by altering the serum levels of inflammatory cytokines and NO.