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Individual and Combined Effects of Selective Cyclooxygenase‐2 Inhibitor and Omega‐3 Fatty Acid on Endotoxin‐Induced Periodontitis in Rats
Author(s) -
Vardar Saynur,
Buduneli Eralp,
Baylas Haluk,
Hüseyinov Berdeli Afig,
Buduneli Nurcan,
Atilla Gül
Publication year - 2005
Publication title -
journal of periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.036
H-Index - 156
eISSN - 1943-3670
pISSN - 0022-3492
DOI - 10.1902/jop.2005.76.1.99
Subject(s) - celecoxib , cyclooxygenase , arachidonic acid , prostaglandin e2 , omega 3 fatty acid , medicine , prostaglandin , periodontitis , endocrinology , fatty acid , chemistry , leukotriene b4 , saline , enzyme , biochemistry , docosahexaenoic acid , inflammation , polyunsaturated fatty acid
Background: The present study was planned to evaluate the individual and combined effects of selective cyclooxygenase‐2 (COX‐2) inhibitor, celecoxib, and omega‐3 fatty acid on the gingival tissue levels of prostaglandin E 2 (PGE 2 ), prostaglandin F 2α (PGF 2α ), leukotriene B4 (LTB4), and platelet activating factor (PAF) in endotoxin‐induced periodontitis in rats. Methods: Experimental periodontitis was induced by repeated injection of Escherichia coli endotoxin (LPS). Forty‐four adult male Sprague‐Dawley rats were divided into five study groups: saline control, LPS, celecoxib, omega‐3 fatty acid, and combination celecoxib and omega‐3 fatty acid. Celecoxib and omega‐3 fatty acid were given either as a single agent or as a combination therapy during 14 days of the study period. At the end of the 2‐week protocol, the rats were sacrificed, the gingival tissues were dissected and extracted, and the extracts were analyzed for PGE 2 , PGF 2α , and LTB 4 levels by enzyme immunoassay and for PAF levels by radioimmunoassay. The defleshed jaws were analyzed morphometrically for alveolar bone loss. Data were evaluated statistically by using parametric tests. Results: LPS injection resulted in significantly more bone loss than the saline controls ( P <0.05) and significant elevations in the gingival tissue levels of all the analyzed mediators except PGF 2α . Individual administration of celecoxib revealed significant reductions in PGE 2 and PAF levels ( P <0.05), while omega‐3 fatty acid provided significant reduction in PGE 2 , PGF 2α , and LTB 4 levels compared to the LPS group ( P <0.05). Combined administration of celecoxib and omega‐3 fatty acid exhibited significantly lower values than those of the LPS group in all the analyzed membrane phospholipid mediators ( P <0.05), which approximated the levels in the saline control group ( P >0.05). Conclusions: The results of the present study indicate that celecoxib and omega‐3 fatty acid, when used individually, show a rather partial effect on the control of the analyzed mediators, but when combined they show a synergic effect and provide significant reductions in the gingival tissue levels of PGE 2 , PGF 2α , LTB 4 , and PAF in LPS‐induced experimental periodontitis. These findings may pioneer further clinical human studies investigating the possible place of celecoxib and omega‐3 fatty acid in periodontal treatment. J Periodontol 2005;76:99‐106 .