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首页> 外文期刊>Experimental Brain Research >Post-activation depression of Soleus stretch reflexes in healthy and spastic humans
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Post-activation depression of Soleus stretch reflexes in healthy and spastic humans

机译:活跃和痉挛性人的比目鱼肌舒展反射后激活抑制

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摘要

Reduced depression of transmitter release from Ia afferents following previous activation (post-activation depression) has been suggested to be involved in the pathophysiology of spasticity. However, the effect of this mechanism on the myotatic reflex and its possible contribution to increased reflex excitability in spastic participants has not been tested. To investigate these effects, we examined post-activation depression in Soleus H-reflex responses and in mechanically evoked Soleus stretch reflex responses. Stretch reflex responses were evoked with consecutive dorsiflexion perturbations delivered at different intervals. The magnitude of the stretch reflex and ankle torque response was assessed as a function of the time between perturbations. Soleus stretch reflexes were evoked with constant velocity (175°/s) and amplitude (6°) plantar flexion perturbations. Soleus H-reflexes were evoked by electrical stimulation of the tibial nerve in the popliteal fossa. The stretch reflex and H-reflex responses of 30 spastic participants (with multiple sclerosis or spinal cord injury) were compared with those of 15 healthy participants. In the healthy participants, the magnitude of the soleus stretch reflex and H-reflex decreased as the interval between the stimulus/perturbation was decreased. Similarly, the stretch-evoked torque decreased. In the spastic participants, the post-activation depression of both reflexes and the stretch-evoked torque was significantly smaller than in healthy participants. These findings demonstrate that post-activation depression is an important factor in the evaluation of stretch reflex excitability and muscle stiffness in spasticity, and they strengthen the hypothesis that reduced post-activation depression plays a role in the pathophysiology of spasticity.
机译:先前的激活(激活后抑制)后,Ia传入递质释放的抑制降低(已被证实)与痉挛的病理生理有关。但是,这种机制对肌反射性反射的作用及其对痉挛性参与者反射反射兴奋性增加的可能贡献尚未得到测试。为了研究这些影响,我们检查了Soleus H反射反应和机械诱发的Soleus拉伸反射反应的激活后抑郁。在不同的时间间隔连续产生背屈摄动引起的舒展反射反应。拉伸反射和踝部扭矩响应的大小被评估为摄动之间的时间的函数。以恒定的速度(175°/ s)和振幅(6°)的足底屈曲摄动引起比目鱼肌的舒张反射。电刺激of窝的胫神经引起比目鱼肌H反射。将30名痉挛性参与者(患有多发性硬化症或脊髓损伤)的拉伸反射和H反射反应与15名健康参与者进行比较。在健康的参与者中,随着刺激/摄动之间的间隔减小,比目鱼肌拉伸反射和H反射的幅度减小。类似地,拉伸诱发的扭矩降低。在痉挛性参与者中,反射后的激活后压低和拉伸诱发的扭矩均显着小于健康参与者。这些发现表明,激活后抑郁症是评估痉挛性牵张反射兴奋性和肌肉僵硬程度的重要因素,并且它们增强了以下假设:激活后抑郁症在痉挛的病理生理中起作用。

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