The collagenase-induced osteoarthritis (CIOA) model: Where mechanical damage meets inflammation

Patrick Weber , Kajetana Bevc , David Fercher , Sami Kauppinen , Shipin Zhang , Maryam Asadikorayem , Lucia Baixauli Marin , Tanqi Zhang , Tuomas Frondelius , Gian Salzmann , Valentino Bruhin , Jakob Hax , Gonçalo Barreto , Mikko A.J. Finnilä , Marcy Zenobi-Wong
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引用次数: 0

Abstract

Objective

To characterize inflammatory and mechanical changes in the collagenase-induced OA (CIOA) model in rats.

Design

Skeletally mature, 6-month-old Wistar rats received unilateral intraarticular injections of saline, 500 U or 1000 U of collagenase on days 0 and 2 of the study. Joint tissues were harvested on either day 4 or 70 to evaluate the acute and long-term changes. Blood biomarkers, gait asymmetry and mechanical hyperalgesia were assessed repeatedly up until day 70.

Results

The intraarticular injection of collagenase triggered an increase in cartilage degeneration and bone resorption over time, particularly for 1000 U. Similarly, mild synovitis was observed on day 70 with an increased number of synovial lining cells, increased fibrosis, and infiltration of peripheral macrophages. Mechanistically, these findings were linked to a dose-related mechanical weakening of the anterior cruciate ligament (ACL), which caused persistent joint destabilization throughout the study. Furthermore, the collagenase injection triggered acute inflammation and swelling of the synovium on day 4 and an acute systemic inflammatory response with increased cytokine and peripheral blood immune cell levels. While mild synovitis persisted until day 70, the systemic inflammatory response returned to control levels after 8 days. Similarly, the observed acute changes in gait and mechanical hyperalgesia also returned to baseline after 21 days.

Conclusion

By evaluating inflammatory and mechanical factors at different doses and timepoints, our characterization enables a more targeted study design and increases the clinical relevance of future studies involving the CIOA model.
胶原酶诱导的骨关节炎(CIOA)模型:机械损伤与炎症的结合
目的描述胶原酶诱导的大鼠 OA(CIOA)模型中的炎症和机械变化。设计6 个月大的骨骼成熟的 Wistar 大鼠在研究的第 0 天和第 2 天接受单侧关节内注射生理盐水、500 U 或 1000 U 的胶原酶。在第 4 天或第 70 天收获关节组织,以评估急性和长期变化。结果关节内注射胶原酶后,随着时间的推移,软骨变性和骨吸收增加,尤其是注射 1000 U 时。同样,在第 70 天观察到轻度滑膜炎,滑膜衬里细胞数量增加,纤维化加重,外周巨噬细胞浸润。从机理上讲,这些发现与前十字韧带(ACL)剂量相关的机械性减弱有关,这种减弱导致整个研究过程中关节持续不稳定。此外,注射胶原酶在第4天引发了滑膜急性炎症和肿胀,以及急性全身炎症反应,细胞因子和外周血免疫细胞水平升高。虽然轻度滑膜炎一直持续到第 70 天,但全身炎症反应在 8 天后恢复到控制水平。同样,观察到的步态急性变化和机械性痛觉减退也在 21 天后恢复到基线水平。结论通过评估不同剂量和时间点的炎症和机械因素,我们的特征描述使研究设计更具针对性,并提高了未来涉及 CIOA 模型研究的临床相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Osteoarthritis and cartilage open
Osteoarthritis and cartilage open Orthopedics, Sports Medicine and Rehabilitation
CiteScore
3.30
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0.00%
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