Abstract
The aims of the present study were, first, to identify signs of alveolar bone damage in early stages of experimental periodontitis (EP) and, second, to assess its possible prevention by treatment with cannabinoid receptor 2 agonist HU 308. Experimental periodontitis was induced by injections of lipopolysaccharide (LPS) (1mg/ml) in gums surrounding maxillary and mandibular first molar, 3 days per week, and untreated controls were kept for comparison. Then, a 3-week study was conducted including eighteen new rats (six rats per group): 1) controls; 2) experimental periodontitis rats; and 3) experimental periodontitis rats treated daily with HU 308 (500 ng/ml). After euthanasia, alveolar bone loss was assessed by morphometric and histomorphometric techniques, and the content of prostaglandin E2 (PGE2) in gingival tissue was evaluated by radioimmunoassay. The first signs of alveolar bone loss were apparent at 3 weeks of experimental periodontitis (ρ<0.05) in the mandibular first molar, but there was no detectable change at 1 week, leading us to establish 3 weeks as an early stage of experimental periodontitis. Rats subjected to 3-week experimental periodontitis showed less interradicular bone volume, less whole bone perimeter and fewer bone formation areas, and higher periodontal space height, bone resorption areas, number of osteoclasts and gingival content of prostaglandin E2 than controls, while HU 308 prevented, at least partially, the deleterious effects (ρ<0.001). We can conclude that a 3-week term of lipopolysaccharide-induced periodontitis in rats provides a valid model of the early stage of the disease, as emerging damage is observed in bone tissue. Furthermore, harmful effects at 3 weeks could be prevented by local stimulation of cannabinoid receptor 2, before greater damage is produced.
Keywords: alveolar bone lossprostaglandin E2, cannabinoids, periodontitis
Sociedad Argentina de Investigación Odontológica.
Conflict of interest statement
none
References
-
- Alshammari AS. Prevalence of different types of gingivitis and periodontitis in patients who attended periodontal clinic in ArAr specialist dental centre, a clinical survey study. Saudi J Oral Dent Res 2017; 2:38-42.
- Stashenko P, Van Dyke T, Tully P, Kent R, Sonis S, Tanner AC. Inflammation and genetic risk indicators for early periodontitis in adults. J Periodontol 2011; 82: 588-596.
- Surkin PN, Ossola CA, Mohn CE, Elverdin JC, Fernández- Solari J. Chronic alcohol consumption alters periodontal health in rats. Alcohol Clin Exp Res 2014; 38: 2001-2007.
- Abul K, Abbas AH, Lichtman JS. Inmunología celular y molecular (2nd ed.). Interamericana, McGraw Hill, 1995, 64-65.
- Bapna M, Chauhan LS. The ambidextrous cyclooxygenase: an enduring target. Inflamm Allergy Drug Targets 2015; 13:387-392.