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Journal of Dental Research
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Biological

Rosiglitazone Reduces the Evolution of Experimental Periodontitis in the Rat

R. Di Paola1, E. Mazzon1, D. Maiere1, D. Zito1, D. Britti2, M. De Majo3, T. Genovese1 and S. Cuzzocrea1,*

1 Department of Clinical and Experimental Medicine and Pharmacology, Torre Biologica, Policlinico Universitario, Via C. Valeria, Gazzi, 98100 Messina, Italy;
2 Department of Clinical Veterinary Science, University of Teramo, Italy; and
3 Department of Clinical Veterinary Medicine and Pharmacology University of Messina, Italy

Correspondence: * corresponding author, salvator{at}unime.it

The peroxisome proliferator-activated receptor-{gamma} (PPAR-{gamma}) receptor appears to play a pivotal role in the regulation of cellular proliferation and inflammation. Recent evidence also suggests that rosiglitazone, a PPAR-{gamma} agonist, reduces acute and chronic inflammation. We hypothesized that rosiglitazone would attenuate periodontal inflammation. In the present study, we investigated the effects of rosiglitazone in a rat model of ligature-induced periodontitis. At day 8, ligation significantly induced an increase in neutrophil infiltration, as well as of gingivomucosal tissue expression of iNOS, nitrotyrosine formation, and poly (ADP-ribose) polymerase activation. Ligation significantly increased Evans blue extravasation in gingivomucosal tissue and alveolar bone destruction. Intraperitoneal injection of rosiglitazone (10 mg/kg 10% DMSO daily for 8 days) significantly decreased all of the parameters of inflammation, as described above. Analysis of these data demonstrated that rosiglitazone exerted an anti-inflammatory role during experimental periodontitis, and was able to ameliorate the tissue damage associated with ligature-induced periodontitis.

Key Words: rosiglitazone • peroxisome proliferator-activated receptor-{gamma} ligand • alveolar bone loss • reactive oxygen species • periodontal diseases

Journal of Dental Research, Vol. 85, No. 2, 156-161 (2006)
DOI: 10.1177/154405910608500208


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