Leni and Peter W May Department of Orthopaedics, Mount Sinai School of Medicine, 5 East 98th Street, 9th Floor, NY 10029, USA.
J Biomech. 2010 Jan 19;43(2):274-9. doi: 10.1016/j.jbiomech.2009.08.039. Epub 2009 Nov 25.
This study describes the development and application of a novel rat patellar tendon model of mechanical fatigue for investigating the early in vivo response to tendon subfailure injury. Patellar tendons of adult female Sprague-Dawley rats were fatigue loaded between 1-35N using a custom-designed loading apparatus. Patellar tendons were subjected to Low-, Moderate- or High-level fatigue damage, defined by grip-to-grip strain measurement. Molecular response was compared with that of a laceration-repair injury. Histological analyses showed that progression of tendon fatigue involves formation of localized kinked fiber deformations at Low damage, which increased in density with presence of fiber delaminations at Moderate damage, and fiber angulation and discontinuities at High damage levels. RT-PCR analysis performed at 1- and 3-day post-fatigue showed variable changes in type I, III and V collagen mRNA expression at Low and Moderate damage levels, consistent with clinical findings of tendon pathology and were modest compared with those observed at High damage levels, in which expression of all collagens evaluated were increased markedly. In contrast, only type I collagen expression was elevated at the same time points post-laceration. Findings suggest that cumulative fatigue in tendon invokes a different molecular response than laceration. Further, structural repair may not be initiated until reaching end-stage fatigue life, where the repair response may unable to restore the damaged tendon to its pre-fatigue architecture.
本研究描述了一种新的大鼠髌腱力学疲劳模型的开发和应用,用于研究早期体内对腱亚失效损伤的反应。使用定制的加载装置,在 1-35N 的范围内对成年雌性 Sprague-Dawley 大鼠的髌腱进行疲劳加载。通过夹持对夹持应变测量来定义髌腱受到低水平、中水平或高水平疲劳损伤。将分子反应与撕裂修复损伤进行比较。组织学分析表明,腱疲劳的进展涉及在低损伤时形成局部扭曲纤维变形,随着中损伤时纤维分层的存在,纤维扭曲和不连续性在高损伤水平增加。在疲劳后 1 天和 3 天进行 RT-PCR 分析显示,I 型、III 型和 V 型胶原 mRNA 表达在低损伤和中损伤水平上发生了不同的变化,与临床腱病理发现一致,与高损伤水平上观察到的变化相比,所有评估的胶原表达都明显增加。相比之下,撕裂后同一时间点仅 I 型胶原表达升高。研究结果表明,腱的累积疲劳会引起与撕裂不同的分子反应。此外,结构修复可能直到达到终末期疲劳寿命才开始,此时修复反应可能无法将受损的腱恢复到疲劳前的结构。