New surgical model of post-traumatic osteoarthritis: Isolated intra-articular bone injury in the rabbit

被引:30
|
作者
Huebner, Kyla D. [1 ]
Shrive, Nigel G. [1 ,2 ]
Frank, Cyril B. [1 ]
机构
[1] Univ Calgary, Fac Med, Dept Surg, McCaig Inst Bone & Joint Hlth, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Schulich Sch Engn, Dept Civil Engn, Calgary, AB T2N 1N4, Canada
基金
加拿大健康研究院;
关键词
knee; surgery; cartilage; bone; osteoarthritis; ANTIGEN-INDUCED ARTHRITIS; ARTICULAR-CARTILAGE; KNEE OSTEOARTHRITIS; INFLAMMATION; EXPRESSION; JOINT;
D O I
10.1002/jor.22284
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
摘要
Osteoarthritis (OA) is a leading cause of disability worldwide. We hypothesized that inflammation following isolated intra-articular bone injury can stimulate post-traumatic OA and developed a rabbit model to test that concept. Sixty female New Zealand White Rabbits were used. Twenty-six experimental animals had two holes drilled into their right femoral-notch, 18 rabbits had sham surgery, and 16 were un-operated controls. Rabbits were euthanized in subgroups at 72h, 3, 6, 9, and 52 weeks. Knees were assessed grossly and tissues collected. Cartilage and synovium were analyzed with histology and qPCR and subgroups compared statistically. All surgical joints showed gross and histological (modified Mankin score) cartilage damage after surgery, with experimentals worsening with time (p<0.05). Cartilage qPCR showed fivefold increases in TGF (p<0.05) expression at 72h and 3 weeks with sixfold increases in MMP13 (p<0.025) expression at 72h. By 6 weeks, expression of these markers was similar to baseline levels. Synovial membrane thickening with increased cellularity was seen at both 9 and 52 weeks (p<0.05). Short-term synovial inflammatory marker (IL-1, IL-Ra, IL-6, and IL-8) expression was three- to fourfold increase in experimentals at 72h (p<0.01) returning to baseline levels by 3 weeks. Intra-articular bone injury creates early joint inflammation with some chronic synovial changes and progressive cartilage damage consistent with OA in adult rabbits. This model provides an exciting new avenue to potentially explore some relevant inflammatory drivers of OA without major mechanical variables. (c) 2013 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 31: 914920, 2013
引用
收藏
页码:914 / 920
页数:7
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