Campbell Stuart G, Campbell Kenneth S
Department of Physiology and the Center for Muscle Biology, University of Kentucky, Lexington, Kentucky.
Biophys Rev. 2011 Dec;3(4):199-207. doi: 10.1007/s12551-011-0059-2.
A skeletal muscle that is stretched while contracting will produce more force at steady state than if it is stretched passively and then stimulated to contract. This phenomenon is known as residual force enhancement and has been widely studied since its description more than sixty years ago. The idea that the mechanical properties of a muscle are governed not just by its present length but also by its length at earlier time points has far reaching implications since muscles stretch and shorten routinely in normal use. In this review, we present the experimental and theoretical advances that have been made toward understanding the mechanisms that underlie residual force enhancement. In the past ten years, experiments and models have focused on essentially three candidate mechanisms for residual force enhancement: (half-) sarcomere inhomogeneity, activity of so-called 'passive' mechanical elements in the sarcomere (titin), and the intrinsic properties of myosin crossbridges. Evidence, both computational and experimental, is accumulating for each of these mechanisms such that a final description of the phenomenon seems attainable in the near future. We conclude that computational models that incorporate more than one putative mechanism may ultimately facilitate reconciliation of the growing number of ideas and experimental data in this field.
一块在收缩时被拉伸的骨骼肌在稳态下产生的力量会比先被被动拉伸然后再被刺激收缩时更大。这种现象被称为残余力增强,自六十多年前被描述以来已得到广泛研究。肌肉的力学特性不仅由其当前长度决定,还受其较早时间点的长度影响,这一观点具有深远意义,因为在正常使用中肌肉会常规性地伸展和缩短。在本综述中,我们介绍了在理解残余力增强背后机制方面取得的实验和理论进展。在过去十年中,实验和模型主要聚焦于残余力增强的三种候选机制:(半)肌节不均匀性、肌节中所谓“被动”力学元件(肌联蛋白)的活性以及肌球蛋白横桥的内在特性。针对这些机制,计算和实验证据都在不断积累,以至于在不久的将来似乎可以对该现象进行最终描述。我们得出结论,纳入不止一种假定机制的计算模型可能最终有助于调和该领域中日益增多的观点和实验数据。