dc.contributor | Universidade Estadual Paulista (Unesp) | |
dc.contributor | Dental School Barry | |
dc.contributor | Federal University of Piauí | |
dc.date.accessioned | 2014-05-27T11:24:51Z | |
dc.date.available | 2014-05-27T11:24:51Z | |
dc.date.created | 2014-05-27T11:24:51Z | |
dc.date.issued | 2010-12-01 | |
dc.identifier | Inflammopharmacology, v. 18, n. 6, p. 293-301, 2010. | |
dc.identifier | 0925-4692 | |
dc.identifier | 1568-5608 | |
dc.identifier | http://hdl.handle.net/11449/71990 | |
dc.identifier | 10.1007/s10787-010-0059-z | |
dc.identifier | 2-s2.0-78651334390 | |
dc.identifier | 4068921369233125 | |
dc.identifier | 4774447118127346 | |
dc.description.abstract | Lumiracoxib is a selective inhibitor of cyclooxygenase-2 (COX-2) approved for the relief of symptoms of chronic inflammatory conditions. The aim of this study was to evaluate the effects of this specific inhibitor of COX-2 as adjunctive treatment on induced periodontitis in rats. Periodontal disease was induced at the first mandibular molar of 60 rats. After 7 days, the ligature was removed and all animals were submitted to scaling and root planing (SRP) along with local irrigation with saline solution and were divided into 2 groups: SRP (n = 30)-received subcutaneous injections of 1 mg/kg of body weight/day of saline solution for 3 days and; SRP + L (n = 30)-received subcutaneous injections of 1 mg/kg of body weight/day of Lumiracoxib for 3 days. Ten animals in each group were killed at 7, 15, and 30 days. The histological description was performed and the histometric values were statistically analyzed. In Group SRP + L, the histometric analysis (0.58 ± 0.08, 0.64 ± 0.06, and 0.56 ± 0.10 mm 2) showed less bone loss (p < 0.05) than Group SRP (1.52 ± 0.08, 1.55 ± 0.09, and 1.49 ± 0.24 mm 2) at 7, 15, and 30 days, respectively. Within the limits of this study it can be concluded that subcutaneous application of specific inhibitor of COX-2 was a beneficial adjunctive treatment for periodontal diseases induced in rats. © 2010 Springer Basel AG. | |
dc.language | eng | |
dc.relation | Inflammopharmacology | |
dc.relation | 3.304 | |
dc.relation | 0,925 | |
dc.relation | 0,925 | |
dc.rights | Acesso restrito | |
dc.source | Scopus | |
dc.subject | Alveolar bone loss | |
dc.subject | Animal studies | |
dc.subject | Lumiracoxib | |
dc.subject | Periodontal disease/therapy | |
dc.subject | Periodontitis | |
dc.subject | Rats | |
dc.subject | collagen fiber | |
dc.subject | cyclooxygenase 2 inhibitor | |
dc.subject | lumiracoxib | |
dc.subject | sodium chloride | |
dc.subject | alveolar bone loss | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | bone tissue | |
dc.subject | controlled study | |
dc.subject | histopathology | |
dc.subject | male | |
dc.subject | morphometrics | |
dc.subject | nonhuman | |
dc.subject | periodontal disease | |
dc.subject | periodontitis | |
dc.subject | preventive dentistry | |
dc.subject | priority journal | |
dc.subject | rat | |
dc.subject | wound irrigation | |
dc.subject | Alveolar Bone Loss | |
dc.subject | Animals | |
dc.subject | Chemotherapy, Adjuvant | |
dc.subject | Cyclooxygenase 2 Inhibitors | |
dc.subject | Dental Scaling | |
dc.subject | Diclofenac | |
dc.subject | Injections, Subcutaneous | |
dc.subject | Male | |
dc.subject | Rats, Wistar | |
dc.subject | Root Planing | |
dc.title | Treatment of experimental periodontal disease by a selective inhibitor of cyclooxygenase-2 with scaling and root planing (SRP) | |
dc.type | Artículos de revistas | |