Wiesendanger M, Rüegg D G, Lucier G E
Can J Neurol Sci. 1975 Aug;2(3):295-301. doi: 10.1017/s0317167100020394.
Experiments in humans and in monkeys have indicated that load perturbations, occurring during voluntary movements and postural activity, may be automatically compensated for. Overall muscle stiffness opposing load changes is determined by the visco-elastic properties of the muscle, by segmental reflex actions and finally by long-loop reflexes. Under certain circumstances, for instance when the subject or the experimental monkey is "prepared" to counteract perturbations which are unpredictable in time, the long-loop "reflexes" appear to be responsible for most of the corrective muscle tension. Experiments in anaesthetized monkeys revealed that signals from stretch afferents reach neurons of the motor cortex, possibly via a relay in the cortical area 3a. The latencies of these responses to well controlled muscle stretches were in the same range as motor cortical cell discharges recorded in alert monkeys subjected to load perturbations. Furthermore, these responses of cells in the motor cortex also had the appropriate timing to indicate a causal relationship with the long-latency electromyographic responses to load changes referred to above. These experimental results therefore strongly support the hypothesis, first proposed by Phillips (1969), of a transcortical servo-loop adjusting motor cortical output according to the load conditions in which movements are performed. The major advantage of transcortical regulations as opposed to segmental regulations, seems to be a powerful gain control acting at the cortical level; it was repeatedly shown that the long-loop reflexes are strongly modifiable and under voluntary control. It is suggested that an adaptive gain control at the cortical level is a prerequisite to preserve the complex capabilities of the motor cortex as the chief "executive" for skilled, preprogrammed movements. A loss of this adaptive gain control may be, at least partly, the cause of motor disorders such as rigidity in Parkinsonian patients, as reported by Tatton and Lee (1975). It is suggested that further investigations of the control of transcortical reflexes may aid in the understanding of the pathophysiology of motor disabilities.
在人类和猴子身上进行的实验表明,在自主运动和姿势活动过程中出现的负荷扰动可能会被自动补偿。对抗负荷变化的整体肌肉僵硬度由肌肉的粘弹性特性、节段性反射作用以及最终的长环反射决定。在某些情况下,例如当受试者或实验猴子“准备好”抵消时间上不可预测的扰动时,长环“反射”似乎是大部分纠正性肌肉张力的原因。对麻醉猴子的实验表明,来自牵张传入神经的信号可能通过皮质3a区的中继到达运动皮质的神经元。这些对精心控制的肌肉牵张的反应潜伏期与在受到负荷扰动的清醒猴子中记录的运动皮质细胞放电潜伏期处于同一范围。此外,运动皮质中细胞的这些反应也具有适当的时间,表明与上述对负荷变化的长潜伏期肌电图反应存在因果关系。因此,这些实验结果有力地支持了菲利普斯(1969年)首次提出的假设,即存在一个跨皮质伺服环路,根据运动时的负荷条件调整运动皮质输出。与节段性调节相比,跨皮质调节的主要优势似乎是在皮质水平起作用的强大增益控制;反复表明长环反射具有很强的可调节性且受自主控制。有人认为,皮质水平的适应性增益控制是保持运动皮质作为熟练、预编程运动的主要“执行者”的复杂能力的先决条件。如塔顿和李(1975年)所报道,这种适应性增益控制的丧失可能至少部分是帕金森病患者出现僵硬等运动障碍的原因。有人认为,对跨皮质反射控制的进一步研究可能有助于理解运动障碍的病理生理学。