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加载率依赖性损伤模式在创伤后骨关节炎小鼠模型中的比较。

Comparison of loading rate-dependent injury modes in a murine model of post-traumatic osteoarthritis.

机构信息

Department of Orthopaedic Surgery, University of California-Davis Medical Center, 4635 2nd Ave, Suite 2000, Sacramento, California, 95817.

出版信息

J Orthop Res. 2014 Jan;32(1):79-88. doi: 10.1002/jor.22480. Epub 2013 Sep 9.

Abstract

Post-traumatic osteoarthritis (PTOA) is a common long-term consequence of joint injuries such as anterior cruciate ligament (ACL) rupture. In this study we used a tibial compression overload mouse model to compare knee injury induced at low speed (1 mm/s), which creates an avulsion fracture, to injury induced at high speed (500 mm/s), which induces midsubstance tear of the ACL. Mice were sacrificed at 0 days, 10 days, 12 weeks, or 16 weeks post-injury, and joints were analyzed with micro-computed tomography, whole joint histology, and biomechanical laxity testing. Knee injury with both injury modes caused considerable trabecular bone loss by 10 days post-injury, with the Low Speed Injury group (avulsion) exhibiting a greater amount of bone loss than the High Speed Injury group (midsubstance tear). Immediately after injury, both injury modes resulted in greater than twofold increases in total AP joint laxity relative to control knees. By 12 and 16 weeks post-injury, total AP laxity was restored to uninjured control values, possibly due to knee stabilization via osteophyte formation. This model presents an opportunity to explore fundamental questions regarding the role of bone turnover in PTOA, and the findings of this study support a biomechanical mechanism of osteophyte formation following injury.

摘要

创伤后骨关节炎(PTOA)是关节损伤(如前交叉韧带(ACL)断裂)的常见长期后果。在这项研究中,我们使用胫骨压缩过载小鼠模型比较了低速(1mm/s)引起的膝关节损伤,这种损伤会导致撕脱性骨折,以及高速(500mm/s)引起的 ACL 中段撕裂。小鼠在损伤后 0 天、10 天、12 周或 16 周时被处死,并用微计算机断层扫描、全关节组织学和生物力学松弛度测试对关节进行分析。两种损伤模式都在损伤后 10 天内导致了相当大的小梁骨丢失,低速损伤组(撕脱)比高速损伤组(中段撕裂)表现出更多的骨丢失。损伤后立即,与对照膝关节相比,两种损伤模式的总 AP 关节松弛度增加了两倍以上。到损伤后 12 周和 16 周时,总 AP 松弛度恢复到未受伤的对照值,这可能是由于骨赘形成导致膝关节稳定。该模型为探索骨转换在 PTOA 中的作用的基本问题提供了机会,本研究的结果支持损伤后骨赘形成的生物力学机制。

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