Department of Development and Rehabilitation of Motor Function, Human Health Sciences, Graduate School of Medicine, Kyoto University.
Department of Motor Function Analysis, Human Health Sciences, Graduate School of Medicine, Kyoto University.
J Vis Exp. 2021 Jul 5(173). doi: 10.3791/62660.
The pathophysiology of primary osteoarthritis (OA) remains unclear. However, a specific subclassification of OA in relatively younger age groups is likely correlated with a history of articular cartilage damage and ligament avulsion. Surgical animal models of OA of the knee play an important role in understanding the onset and progression of post-traumatic OA and aid in the development of novel therapies for this disease. However, non-surgical models have been recently considered to avoid traumatic inflammation that could affect the evaluation of the intervention. In this study, an intra-articular cartilage lesion rat model induced by in vivo cyclic compressive loading was developed, which allowed researchers to (1) determine the optimal magnitude, speed, and duration of load that could cause focal cartilage damage; (2) assess post-traumatic spatiotemporal pathological changes in chondrocyte vitality; and (3) evaluate the histological expression of destructive or protective molecules that are involved in the adaptation and repair mechanisms against joint compressive loads. This report describes the experimental protocol for this novel cartilage lesion in a rat model.
原发性骨关节炎(OA)的病理生理学仍不清楚。然而,在相对年轻的年龄组中,OA 的特定亚分类可能与关节软骨损伤和韧带撕脱的病史相关。膝关节 OA 的外科动物模型在理解创伤后 OA 的发病和进展方面发挥着重要作用,并有助于为这种疾病开发新的治疗方法。然而,最近已经考虑使用非外科模型来避免可能影响干预评估的创伤性炎症。在这项研究中,通过体内循环压缩加载建立了一种关节内软骨损伤大鼠模型,该模型允许研究人员:(1)确定能导致局灶性软骨损伤的最佳负荷大小、速度和持续时间;(2)评估创伤后软骨细胞活力的时空病理变化;以及 (3)评估涉及关节压缩负荷适应和修复机制的破坏性或保护性分子的组织学表达。本报告介绍了这种新型软骨损伤在大鼠模型中的实验方案。