Nielsen J, Kagamihara Y, Crone C, Hultborn H
Institute of Neurophysiology, Panum Institute, University of Copenhagen, Denmark.
Exp Brain Res. 1992;88(3):651-6. doi: 10.1007/BF00228194.
Recent studies have reported that no increase of the disynaptic reciprocal inhibition can be observed during tonic voluntary dorsiflexion of the foot as compared to rest, when the size of the control H-reflex is kept constant. Other studies have, however, shown that a voluntary contraction evokes a strong and long-lasting depression of the synaptic transmission from Ia afferents to motoneurones, most likely secondary to activation of these afferents during the contraction (post-activation depression). It was thought that this effect could also interfere with the demonstration of a central facilitation of the reciprocal inhibition during movement. The amount of disynaptic Ia reciprocal inhibition from the pretibial flexors to the soleus H-reflex was therefore estimated in normal human subjects at rest and during voluntary tonic dorsiflexion before, during and after blocking the peripheral feedback from the investigated muscles. It was observed that the reciprocal inhibition measured during dorsiflexion increased during occlusion of the blood supply to the leg, reaching a maximum of inhibition after 30 min of ischaemia. After release of the ischaemia the inhibition gradually decreased to its pre-ischaemic level. It is therefore suggested that the brain facilitates transmission in the Ia disynaptic reciprocal pathway during tonic voluntary dorsiflexion of the foot, but that this facilitation is normally not observed due to a post-activation depression following the peripheral feedback activation during the movement.
最近的研究报告称,当对照H反射的大小保持恒定时,与静息状态相比,在足部强直性随意背屈期间未观察到双突触交互抑制增加。然而,其他研究表明,随意收缩会引起从Ia传入纤维到运动神经元的突触传递强烈且持久的抑制,这很可能继发于收缩过程中这些传入纤维的激活(激活后抑制)。人们认为这种效应也可能干扰运动期间交互抑制的中枢易化的表现。因此,在正常人类受试者中,在阻断被研究肌肉的外周反馈之前、期间和之后,分别在静息状态和随意强直性背屈期间,估计了从胫骨前屈肌到比目鱼肌H反射的双突触Ia交互抑制量。观察到在背屈期间测量的交互抑制在腿部血液供应阻断期间增加,在缺血30分钟后达到最大抑制。缺血解除后,抑制逐渐降至缺血前水平。因此,有人提出,在足部强直性随意背屈期间,大脑促进Ia双突触交互通路中的传递,但由于运动期间外周反馈激活后的激活后抑制,这种易化通常未被观察到。