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跖肌腱和鼠尾肌腱的多尺度加载和损伤机制。

Multi-Scale Loading and Damage Mechanisms of Plantaris and Rat Tail Tendons.

机构信息

Department of Biomedical Engineering, University of Delaware, Newark, Delaware 19716.

出版信息

J Orthop Res. 2019 Aug;37(8):1827-1837. doi: 10.1002/jor.24309. Epub 2019 May 2.

Abstract

Tendinopathy, degeneration of the tendon that leads to pain and dysfunction, is common in both sports and occupational settings, but multi-scale mechanisms for tendinopathy are still unknown. We recently showed that micro-scale sliding (shear) is responsible for both load transfer and damage mechanisms in the rat tail tendon; however, the rat tail tendon is a specialized non-load-bearing tendon, and thus the load transfer and damage mechanisms are still unknown for load-bearing tendons. The objective of this study was to investigate the load transfer and damage mechanisms of load-bearing tendons using the rat plantaris tendon. We demonstrated that micro-scale sliding is a key component for both mechanisms in the plantaris tendon, similar to the tail tendon. Namely, the micro-scale sliding was correlated with applied strain, demonstrating that load was transferred via micro-scale sliding in the plantaris and tail tendons. In addition, while the micro-scale strain fully recovered, the micro-scale sliding was non-recoverable and strain-dependent, and correlated with tissue-scale mechanical parameters. When the applied strain was normalized, the % magnitudes of non-recoverable sliding was similar between the plantaris and tail tendons. Statement of clinical significance: Understanding the mechanisms responsible for the pathogenesis and progression of tendinopathy can improve prevention and rehabilitation strategies and guide therapies and the design of engineered constructs. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:1827-1837, 2019.

摘要

腱病,即肌腱的退化,导致疼痛和功能障碍,在运动和职业环境中都很常见,但腱病的多尺度机制仍不清楚。我们最近表明,微尺度滑动(剪切)负责大鼠尾腱的负载传递和损伤机制;然而,大鼠尾腱是一种特殊的非承重肌腱,因此承重肌腱的负载传递和损伤机制仍不清楚。本研究的目的是使用大鼠跖肌腱研究承重肌腱的负载传递和损伤机制。我们证明,微尺度滑动是跖肌腱和尾腱这两种机制的关键组成部分。也就是说,微尺度滑动与施加的应变相关,表明负载通过跖肌腱和尾肌腱的微尺度滑动传递。此外,虽然微尺度应变完全恢复,但微尺度滑动是不可恢复的,且与应变相关,与组织尺度的力学参数相关。当施加的应变归一化时,跖肌腱和尾肌腱的不可恢复滑动的幅度百分比相似。临床意义的声明:了解导致腱病发病和进展的机制可以改善预防和康复策略,并指导治疗和工程构建的设计。版权所有 © 2019 矫形研究协会。由 Wiley Periodicals, Inc. 出版。J 矫形研究 37:1827-1837, 2019.

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