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Temporal Effect of In Vivo Tendon Fatigue Loading on the Apoptotic Response Explained in the Context of Number of Fatigue Loading Cycles and Initial Damage Parameters

机译:在疲劳加载循环次数和初始损伤参数的背景下体外肌腱疲劳加载对细胞凋亡反应的时间效应

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摘要

Accumulation of damage is a leading factor in the development of tendinopathy. Apoptosis has been implicated in tendinopathy, but the biological mechanisms responsible for initiation and progression of these injuries are poorly understood. We assessed the relationship between initial induced damage and apoptotic activity 3 and 7 days after fatigue loading. We hypothesized that greater apoptotic activity (i) will be associated with greater induced damage and higher number of fatigue loading cycles, and (ii) will be higher at 7 than at 3 days after loading. Left patellar tendons were fatigue loaded for either 100 or 7,200 cycles. Diagnostic tests were applied before and after fatigue loading to determine the effect of fatigue loading on hysteresis, elongation, and loading and unloading stiffness (damage parameters). Cleaved Caspase-3 staining was used to identify and calculate the percent apoptosis in the patellar tendon. While no difference in apoptotic activity occurred between the 100 and 7,200 cycle groups, greater apoptotic activity was associated with greater induced damage. Apoptotic activity was higher at 7 than 3 days after loading. We expect that the decreasing number of healthy cells that can repair the induced damage in the tendon predispose it to further injury.
机译:损伤的积累是肌腱病发展的主要因素。细胞凋亡与肌腱病有关,但是导致这些损伤的发生和发展的生物学机制却鲜为人知。我们评估了疲劳负荷后第3天和第7天初始诱导损伤与凋亡活动之间的关系。我们假设更大的凋亡活性(i)与更大的诱导损伤和更高的疲劳负荷循环次数相关,并且(ii)在负荷后7天比在负荷后3天更高。左pa肌腱承受100或7,200个周期的疲劳负荷。在疲劳载荷之前和之后进行诊断测试,以确定疲劳载荷对滞后,伸长以及载荷和载荷刚度(损伤参数)的影响。切开的Caspase-3染色用于鉴定和计算the腱中的凋亡百分比。虽然在100和7,200个周期组之间凋亡活性没有差异,但是更大的凋亡活性与更大的诱导损伤相关。加载后3天,细胞凋亡活性高于7天。我们期望可以修复肌腱诱发的损伤的健康细胞数量减少,使其更易受伤。

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