Rassier Dilson E, Herzog Walter
Human Performance Laboratory, Faculty of Kinesiology, University of Calgary, Calgary, Alberta, Canada T2N 1N4.
J Appl Physiol (1985). 2004 Feb;96(2):419-27. doi: 10.1152/japplphysiol.00653.2003.
When a skeletal muscle that is actively producing force is shortened or stretched, the resulting steady-state isometric force after the dynamic phase is smaller or greater, respectively, than the purely isometric force obtained at the corresponding final length. The cross-bridge model of muscle contraction does not readily explain this history dependence of force production. The most accepted proposal to explain both, force depression after shortening and force enhancement after stretch, is a nonuniform behavior of sarcomeres that develops during and after length changes. This hypothesis is based on the idea of instability of sarcomere lengths on the descending limb of the force-length relationship. However, recent evidence suggests that skeletal muscles may be stable over the entire range of active force production, including the descending limb of the force-length relationship. The purpose of this review was to critically evaluate hypotheses aimed at explaining the history dependence of force production and to provide some novel insight into the possible mechanisms underlying these phenomena. It is concluded that the sarcomere nonuniformity hypothesis cannot always explain the total force enhancement observed after stretch and likely does not cause all of the force depression after shortening. There is evidence that force depression after shortening is associated with a reduction in the proportion of attached cross bridges, which, in turn, might be related to a stress-induced inhibition of cross-bridge attachment in the myofilament overlap zone. Furthermore, we suggest that force enhancement is not associated with instability of sarcomeres on the descending limb of the force-length relationship and that force enhancement has an active and a passive component. Force depression after shortening and force enhancement after stretch are likely to have different origins.
当一块正在主动发力的骨骼肌被缩短或拉伸时,动态阶段之后产生的稳态等长力分别小于或大于在相应最终长度下获得的纯等长力。肌肉收缩的横桥模型难以解释这种力产生的历史依赖性。为了解释缩短后的力下降和拉伸后的力增强这两种现象,最被认可的观点是肌节在长度变化期间及之后会出现非均匀行为。这一假设基于力-长度关系下降支上肌节长度不稳定的观点。然而,最近的证据表明,骨骼肌在主动力产生的整个范围内可能都是稳定的,包括力-长度关系的下降支。本综述的目的是批判性地评估旨在解释力产生的历史依赖性的假设,并对这些现象背后的可能机制提供一些新的见解。得出的结论是,肌节非均匀性假设不能总是解释拉伸后观察到的总力增强现象,而且可能不是缩短后所有力下降的原因。有证据表明,缩短后的力下降与附着横桥比例的降低有关,而这反过来可能与应力诱导的肌丝重叠区横桥附着抑制有关。此外,我们认为力增强与力-长度关系下降支上肌节的不稳定性无关,并且力增强有一个主动成分和一个被动成分。缩短后的力下降和拉伸后的力增强可能有不同的起源。