Kostyukov A I
Department of Movement Physiology, A. A. Bogomoletz Institute of Physiology, National Academy of Sciences, Kiev, Ukraine.
Neuroscience. 1998 Mar;83(1):303-20. doi: 10.1016/s0306-4522(97)00379-5.
In this study we have tried to elaborate necessary theoretical approaches for the adequate analysis of the central motor commands to a mammalian muscle in the equilibrium states and during transition movements between these states. At present, the equilibrium point hypothesis has obtained a wide distribution in this field. The muscle is considered in the framework of the theory as an executive element of the reflex circuits originating in the muscle proprioceptors and being closed at the level of spinal cord and the supraspinal motor centres. The main parameter defining the muscle state is supposed to be the threshold of the stretch reflex--the minimal length value at which muscle begins to resist to the externally applied force. We have attempted to show that the theory has an essential shortcoming because it does not take into account such important non-linearity in the muscle behaviour as hysteresis. In the framework of the equilibrium point hypothesis, the muscle behaviour within the stretch reflex system does not depend on movement direction. The stretch and unloading reflexes are supposed to have the same length tension dependencies when the muscle is stretching or contracting with a rather slow velocity. However, powerful hysteresis of the stretch reflex system requires taking into account the direction of the current movement, the after-effects of previous movement led to a principal uncertainty in the muscle steady-state. We would like to stress that any process of active muscle shortening should be controlled by dynamic components in efferent inflow. At the same time, the resulting steady-state develops by using effective hysteresis mechanism for its maintenance. The following hypothesis was proposed to explain the length clamping mechanisms in shortening transition movements. A significant decrement of the arrived efferent activity at the phase of the length fixation can evoke an internal elongation of the contractile elements within the muscle and corresponding hysteresis-like enhancement of the contractile effectiveness. Hence, instead of considering the quasi-static and dynamic components of movement commands as in the equilibrium point hypothesis, it is preferable to adopt a model of the shared coding of both the final position and movement velocity. The dynamic component of the efferent discharge seems to be required for a complete definition of the final steady-state, but maintenance of the state is closely associated with energetically advantageous hysteresis mechanisms. It was concluded that the dynamic phase of efferent activity should play an extremely important role in the central coding of the real movements produced, in particular, by contraction of agonists in the absence of antagonist activation.
在本研究中,我们试图阐述必要的理论方法,以便对哺乳动物肌肉在平衡状态以及这些状态之间的过渡运动期间的中枢运动指令进行充分分析。目前,平衡点假说在该领域已得到广泛传播。在该理论框架下,肌肉被视为反射回路的执行元件,这些反射回路起源于肌肉本体感受器,并在脊髓和脊髓上运动中枢水平形成闭环。定义肌肉状态的主要参数被认为是牵张反射阈值——肌肉开始抵抗外部施加力时的最小长度值。我们试图表明该理论存在一个基本缺陷,因为它没有考虑到肌肉行为中诸如滞后现象这样重要的非线性因素。在平衡点假说框架内,牵张反射系统中的肌肉行为不依赖于运动方向。当肌肉以相当缓慢的速度伸展或收缩时,牵张反射和卸载反射被认为具有相同的长度 - 张力依赖性。然而,牵张反射系统强大的滞后现象要求考虑当前运动的方向,先前运动的后效导致肌肉稳态存在主要的不确定性。我们想强调的是,任何主动肌肉缩短过程都应由传出输入中的动态成分控制。同时,通过使用有效的滞后机制来维持所产生的稳态。为了解释缩短过渡运动中的长度钳制机制,提出了以下假说。在长度固定阶段到达的传出活动显著减少可引发肌肉内收缩元件的内部伸长以及收缩效能相应的类似滞后现象的增强。因此,与其像平衡点假说那样考虑运动指令的准静态和动态成分,不如采用一种同时编码最终位置和运动速度的共享编码模型。传出放电的动态成分似乎对于完整定义最终稳态是必需的,但该状态的维持与能量上有利的滞后机制密切相关。得出的结论是,传出活动的动态阶段在特别是在没有拮抗肌激活的情况下由主动肌收缩产生的实际运动的中枢编码中应发挥极其重要的作用。