Effects of curcumin on crevicular levels of IL-1β and CCL28 in experimental gingivitis

被引:31
作者
Pulikkotil, S. J. [1 ]
Nath, S. [2 ]
机构
[1] Int Med Univ, Sch Dent, Dept Restorat Dent, Kuala Lumpur 57000, Malaysia
[2] Vananchal Dent Coll & Hosp, Dept Periodontol, Garhwa, Jharkhand, India
关键词
CCL28; curcumin; curcuma longa; gingivitis; inflammation; interleukin-1beta; NECROSIS-FACTOR-ALPHA; PERIODONTAL-DISEASE; FLUID; INTERLEUKIN-1-BETA; PREVENTION; MANAGEMENT; THERAPIES; AGENTS; PLAQUE; SERUM;
D O I
10.1111/adj.12340
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BackgroundCurcumin has anti-inflammatory properties. The aim of this study was to compare interleukin-1 (IL-1) and chemokine (C-C motif) ligand 28 (CCL28) levels following a topical application of curcumin (CRM), chlorhexidine (CHX) and chlorhexidine-metronidazole (CHX-MTZ) in an experimental gingivitis human model. MethodsSixty systemically healthy selected subjects were randomly assigned to one of three topical antigingivitis gels. Each gel was applied twice daily for 10minutes as the sole method of oral hygiene for 29days on the test quadrant only. Modified gingival index (MGI), plaque index (PI), bleeding on probing (BOP) and probing depth (PD) were assessed at baseline, 29days and 60days. Estimation of IL-1 and CCL28 levels in gingival crevicular fluid was done at baseline and at 29days. ResultsThe increase of IL-1 in the CRM (14.5216.6pg/ml) and CHX-MTZ (31.63 +/- 15.96) groups was significantly less than that of the CHX group (70.55 +/- 38.81). Similar results were also observed for CCL28 (CRM: 8.12 +/- 8.78pg/ml; CHX-MTZ: 12.81 +/- 18.68; CHX: 41.15 +/- 22.82). All groups had a significant increase in MGI, PI and BOP at 29days. ConclusionsThe anti-inflammatory potential of topical curcumin was similar to CHX-MTZ but superior to CHX in affecting IL-1 and CCL28 levels.
引用
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页码:317 / 327
页数:11
相关论文
共 48 条
[1]  
Aggarwal BB, 2007, ADV EXP MED BIOL, V595, P1
[2]   ON THE PREVENTION OF CARIES AND PERIODONTAL-DISEASE - RESULTS OF A 15-YEAR LONGITUDINAL-STUDY IN ADULTS [J].
AXELSSON, P ;
LINDHE, J ;
NYSTROM, B .
JOURNAL OF CLINICAL PERIODONTOLOGY, 1991, 18 (03) :182-189
[3]  
Behal Roobal, 2011, J Indian Soc Periodontol, V15, P35, DOI 10.4103/0972-124X.82264
[4]  
Berglund T, 2000, J CLIN PERIODONTOL, V20, P179
[5]   AGENTS FOR THE MANAGEMENT OF PLAQUE AND GINGIVITIS [J].
CIANCIO, SG .
JOURNAL OF DENTAL RESEARCH, 1992, 71 (07) :1450-1454
[6]  
Cochran D, 2001, J PERIODONTOL, V72, P1790
[7]   Periodontal diseases in Asia and Oceania [J].
Corbet, EF ;
Zee, KY ;
Lo, ECM .
PERIODONTOLOGY 2000, 2002, 29 :122-152
[8]   Comparison of experimental gingivitis with persistent gingivitis: differences in clinical parameters and cytokine concentrations [J].
Deinzer, R. ;
Weik, U. ;
Kolb-Bachofen, V. ;
Herforth, A. .
JOURNAL OF PERIODONTAL RESEARCH, 2007, 42 (04) :318-324
[9]   Epithelial inflammation is associated with CCL28 production and the recruitment of regulatory T cells expressing CCR10 [J].
Eksteen, Bertus ;
Miles, Alice ;
Curbishley, Stuart M. ;
Tselepis, Chris ;
Grant, Allister J. ;
Walker, Lucy S. K. ;
Adams, David H. .
JOURNAL OF IMMUNOLOGY, 2006, 177 (01) :593-603
[10]   Comparison of CCL28, interleukin-8, interleukin-1β and tumor necrosis factor-alpha in subjects with gingivitis, chronic periodontitis and generalized aggressive periodontitis [J].
Ertugrul, A. S. ;
Sahin, H. ;
Dikilitas, A. ;
Alpaslan, N. ;
Bozoglan, A. .
JOURNAL OF PERIODONTAL RESEARCH, 2013, 48 (01) :44-51