Title of article :
Effects of Angipars on oxidative inflammatory indices in a murine model of periodontitis
Author/Authors :
Mousavi-Jazi, M. tehran university of medical sciences tums - School of Dentistry and Dental Research Center - Department of Periodontology, تهران, ايران , Aslroosta, H. tehran university of medical sciences tums - School of Dentistry and Dental Research Center - Department of Periodontology, تهران, ايران , Moayer, A.R. islamic azad university - School of Dentistry - Department of Periodontology, ايران , Baeeri, M. tehran university of medical sciences tums - Faculty of Pharmacy, and Pharmaceutical Science Research Center, تهران, ايران , Abdollahi, M. tehran university of medical sciences tums - Faculty of Pharmacy - Pharmaceutical Sciences Research Center, تهران, ايران
From page :
260
To page :
264
Abstract :
Background and the purpose of the study: There are strong evidences linking overproduction of reactive oxygen species and periodontal diseases. The aim of this study was to evaluate efficacy of Angipars a natural potent anti oxidative agent on markers of the oxidative damages and periodontal inflammation in the rat.Methods: Periodontitis was induced by single injection of lipopolysaccharide (LPS) from E. coli (10 μg/μl saline) into rat mandibular gingiva. After 10 days, animals in the test group received Angipars (2.1 mg/kg) by gavage once a day and those of control group received same amount of vehicle. The amount of interleukin (IL)-1β, lipid peroxidation (LPO), and 8-hydroxydeoxyguanosine (8-OHdG) were measured in gingival biopsy samples and the degree of apical migration of junctional epithelium (JE), alveolar bone resorption, and the number of polymorphonuclears (PMN) were evaluated by histological analysis of block samples of the left mandibular first molars.Results: Periodontitis group showed a significant increase in periodontal IL-1β, LPO, 8-OHdG, apical migration of JE, alveolar bone resorption and number of PMNs. Angipars treatment resulted in a significant decrease in gingival IL-1β, LPO, 8-OHdG and the apical migration of JE; however, the reduction of alveolar bone resorption was not significant. The number of PMN increased significantly after treatment with Angipars. While intake of vehicle resulted in a significant decrease in gingival IL-1β and LPO, the reduction of 8-OHdG, apical migration of JE, and alveolar bone resorption were not significant. Interestingly, PMNs were increased in groups received Angipars or the vehicle. Conclusion: From the results of this study, it seems that Angipars is beneficial in periodontitis by reduction of inflammatory and oxidative damage. Unexpected increase of PMN count by Angipars strengthens the hypothesis that chronic inflammatory disorders like periodontitis may need more time to get best advantage of anti oxidative drugs like Angipars. Regarding role of microbes in pathogenesis of periodontitis, further studies should be focused on antimicrobial effects of Angipars
Keywords :
Periodontitis , Oxidative stress , Natural medicine
Journal title :
Daru:Journal of Pharmaceutical Sciences
Journal title :
Daru:Journal of Pharmaceutical Sciences
Record number :
2551756
Link To Document :
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