A simulation study of reflex instability in spasticity: origins of clonus.

J M Hidler, W Z Rymer
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引用次数: 72

Abstract

Clonus is defined as an involuntary rhythmic muscle contraction that generally occurs in people who have sustained lesions involving descending motor pathways in the neuraxis, and is usually accompanied by other signs of reflex hyperexcitability such as spasticity. This paper hypothesizes that clonus arises when two conditions occur simultaneously: 1) the reflex pathway contains long delay times (implying innervation of distal limb muscles, exacerbated when these muscles display slow twitch properties) and 2) the excitability of the motoneurons is enhanced. This paper tested this dual hypothesis by developing a computer model representing the ankle reflex pathway. This model included the ankle muscles, afferent and efferent pathways, and a monosynaptic spinal link between spindle afferents and motoneurons. Simulations show that as the motoneuron current threshold was reduced (reflecting increased excitability of spinal motoneurons), normal reflex responses became unstable and oscillations developed similar to those observed in spastic patients. In parallel, when we choose reflex delay times typical for distal leg muscles in man, system stability is poor, and oscillations occur readily with increasing motoneuron excitability. As simulated pathway delays are reduced, oscillatory behavior is also reduced, and usually damps out. Conversely, as simulated reflex delays are increased, oscillations increase in amplitude and do not decay. Finally, these two phenomena interact, so that increasing motoneuron excitability will induce reflex oscillations for intermediate loop delays. These findings support the hypothesis that unstable oscillatory behavior, such as the oscillations observed in clonus, will occur when the motoneuron excitability increases in a reflex pathway containing long delays. This change in excitability is mediated by a reduction in motoneuron firing threshold, rather than by an increase in feedback gain. Furthermore, we demonstrate that sustained oscillations occur readily through self reexcitation, which reduces the need to propose that a "central oscillator" must be involved in generating clonus.

痉挛时反射不稳定性的模拟研究:冠状肌的起源。
Clonus被定义为一种不自主的节律性肌肉收缩,通常发生在持续病变涉及神经轴的下行运动通路的人群中,通常伴有其他反射性亢进的迹象,如痉挛。本文假设,当两种情况同时发生时,会产生clonus: 1)反射通路包含较长的延迟时间(意味着远端肢体肌肉的神经支配,当这些肌肉表现出缓慢的抽搐特性时加剧)和2)运动神经元的兴奋性增强。本文通过开发一个代表踝关节反射通路的计算机模型来验证这一双重假设。该模型包括踝关节肌肉、传入和传出通路,以及纺锤体传入和运动神经元之间的单突触脊髓连接。模拟表明,随着运动神经元电流阈值的降低(反映脊髓运动神经元兴奋性的增加),正常的反射反应变得不稳定,并且出现与痉挛患者相似的振荡。同时,当我们选择人类远端腿部肌肉典型的反射延迟时间时,系统稳定性较差,并且随着运动神经元兴奋性的增加,振荡很容易发生。随着模拟路径延迟的减少,振荡行为也减少了,并且通常会衰减。相反,随着模拟反射延迟的增加,振荡幅度增加而不衰减。最后,这两种现象相互作用,因此运动神经元兴奋性的增加将引起中间环路延迟的反射振荡。这些发现支持了一种假设,即当运动神经元兴奋性在包含长延迟的反射通路中增加时,就会发生不稳定的振荡行为,例如在冠状细胞中观察到的振荡。这种兴奋性的变化是由运动神经元放电阈值的降低介导的,而不是通过反馈增益的增加。此外,我们证明了持续振荡很容易通过自再激励发生,这减少了提出必须有一个“中心振荡器”参与产生克隆的需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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