Herzog Walter
Human Performance Laboratory, Faculty of Kinesiology, University of Calgary , Calgary, Alberta , Canada.
J Appl Physiol (1985). 2019 Jun 1;126(6):1782-1789. doi: 10.1152/japplphysiol.00676.2018. Epub 2019 May 9.
Passive force enhancement is defined as the increase in passive, steady-state, isometric force of an actively stretched muscle compared with the same muscle stretched passively to that same length. Passive force enhancement is long lasting, increases with increasing muscle length and increasing stretch magnitudes, contributes to the residual force enhancement in skeletal and cardiac muscle, and is typically only observed at muscle lengths at which passive forces occur naturally. Passive force enhancement is typically equal to or smaller than the total residual force enhancement, it persists when a muscle is deactivated and reactivated, but can be abolished instantaneously when a muscle is shortened quickly from its stretched length. There is strong evidence that the passive force enhancement is caused by the filamentous sarcomeric protein titin, although the detailed molecular mechanisms underlying passive force enhancement remain unknown. Here I propose a tentative mechanism based on experimental evidence that associates passive force enhancement with the shortening of titin's free spring length in the I-band region of sarcomeres. I suggest that this shortening is accomplished by titin binding to actin and that the trigger for titin-actin interactions is associated with the formation of strongly bound cross bridges between actin and myosin that exposes actin attachment sites for titin through movement of the regulatory proteins troponin and tropomyosin.
被动力量增强被定义为与被动拉伸至相同长度的同一块肌肉相比,主动拉伸的肌肉在被动、稳态等长力方面的增加。被动力量增强持续时间长,随着肌肉长度增加和拉伸幅度增大而增加,对骨骼肌和心肌的残余力量增强有贡献,并且通常仅在自然出现被动力的肌肉长度时观察到。被动力量增强通常等于或小于总的残余力量增强,当肌肉失活并重新激活时它持续存在,但当肌肉从其拉伸长度快速缩短时可以瞬间消除。有强有力的证据表明被动力量增强是由丝状肌节蛋白肌联蛋白引起的,尽管被动力量增强背后的详细分子机制仍然未知。在此,我基于实验证据提出一种初步机制,该机制将被动力量增强与肌节I带区域中肌联蛋白自由弹簧长度的缩短联系起来。我认为这种缩短是通过肌联蛋白与肌动蛋白结合来实现的,并且肌联蛋白 - 肌动蛋白相互作用的触发与肌动蛋白和肌球蛋白之间形成强结合横桥有关,这种横桥通过调节蛋白肌钙蛋白和原肌球蛋白的移动暴露了肌联蛋白的肌动蛋白附着位点。