Dexamethasone Inhibits Inflammation and Cartilage Damage in a New Model of Post-Traumatic Osteoarthritis

被引:131
作者
Huebner, Kyla D. [1 ,2 ]
Shrive, Nigel G. [1 ,3 ]
Frank, Cyril B. [1 ,4 ]
机构
[1] Univ Calgary, Fac Med, McCaig Inst Bone & Joint Hlth, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Fac Med, Dept Med Sci, Calgary, AB T2N 4N1, Canada
[3] Univ Calgary, Schulich Sch Engn, Dept Civil Engn, Calgary, AB T2N 4N1, Canada
[4] Foothills Med Ctr, Alberta Hlth Serv, Dept Surg, Calgary, AB T2N 2T9, Canada
基金
加拿大健康研究院;
关键词
knee; dexamethasone; cartilage; corticosteroids; OA; CORTICOSTEROID INJECTION; ARTICULAR CHONDROCYTES; GENE-EXPRESSION; RABBIT KNEE; ARTHRITIS; INTERLEUKIN-1-BETA; MODULATION; RECEPTOR; RELEASE; MARKERS;
D O I
10.1002/jor.22568
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Corticosteroids are used in musculoskeletal diseases, and offer patient relief. Injections of corticosteroids are recommended for management of osteoarthritis (OA). Current data have shown the role of corticosteroids in ameliorating pain. We hypothesized that repeated intra-articular injections of high dose dexamethasone would protect the cartilage from damage in a post-traumatic model of OA. Eighteen female New Zealand White rabbits were used. Twelve underwent surgery to induce OA; six of them received intra-articular injections of dexamethasone every 3 days for 3 weeks. The other six rabbits served as operated controls. Six additional rabbits served as non-operated controls. All animals were euthanized 3 weeks post-surgery. Knees were assessed grossly. Cartilage, synovium, and fat pad were assessed histologically. Synovium and fat pad were analyzed with qPCR and Western blots. Surgical controls had cartilage damage which was supressed with dexamethasone. Dexamethasone significantly decreased synovial expression of interleukin-1 and collagen I, and a trend to decrease synovial matrix metalloproteinase3 expression. There were also significantly lower levels of interleukin-1 protein with dexamethasone treatment. Dexamethasone significantly decreased fat pad expression of matrix metalloproteinase13, basic fibroblast growth factor, and interleukin8, and a trend to decrease matrix metalloproteinase3 and transforming growth factor expression. Dexamethasone decreased joint inflammation and joint tissue degradation and was chondroprotective in this unique model of PTOA. (c) 2013 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 32:566-572, 2014.
引用
收藏
页码:566 / 572
页数:7
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