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Early response to tendon fatigue damage accumulation in a novel in vivo model
Authors:David T Fung  Vincent M Wang  Nelly Andarawis-Puri  Jelena Basta-Pljakic  Yonghui Li  Damien M Laudier  Hui B Sun  Karl J Jepsen  Mitchell B Schaffler  Evan L Flatow
Institution:1. Department of Biomedical Engineering, Washington University in St. Louis, 1 Brookings Drive, MSC: 1185-208-125, St. Louis, MO 63130, United States;2. Department of Mechanical Engineering and Materials Science, Washington University in St. Louis, United States;3. Department of Biology, Washington University in St. Louis, United States;4. Department of Mechanical Engineering, Massachusetts Institute of Technology, United States;5. Department of Physical Therapy, Washington University in St. Louis School of Medicine, United States;6. Department of Mathematics, Brigham Young University - Idaho, United States;7. Department of Orthopaedic Surgery, Washington University in St. Louis School of Medicine, , United States
Abstract: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 1–35 N 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.
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