Corticospinal control of spinal reflex plasticity

皮质脊髓对脊髓反射可塑性的控制

基本信息

项目摘要

Spinal cord injury (SCI), traumatic brain injury, stroke, multiple sclerosis, and other chronic disorders produce abnormal reflexes that impair locomotion, reach-and-grasp, and other motor functions for millions of Americans, including many Veterans. New treatments are urgently needed. Operant conditioning protocols can change spinal reflexes in rats, mice, monkeys, and people. These protocols, which are non-invasive in humans, can target beneficial plasticity to a specific reflex pathway. The reflex is elicited and the subject is rewarded if the reflex satisfies a size criterion. The subject learns to modify corticospinal control over the pathway. This control gradually changes the spinal pathway itself, and thereby triggers further beneficial plasticity elsewhere. In people with incomplete SCI, operant conditioning of the soleus H-reflex increases walking speed and reduces limping. The improvements persist; they are apparent to people in their daily lives. {Reflex conditioning in people with SCI or stroke now requires 36 one-hr sessions over 12 weeks, and is successful in only 50-70%.} Better understanding of the cortical activity that drives the reflex change should lead to better protocols that increase the reliability, magnitude, and speed of reflex conditioning, and thereby enhance its clinical value. This project seeks to identify electroencephalographic (EEG) features that reflect the crucial cortical activity, to use these features to improve the reflex conditioning protocol, {and to show that this protocol is effective in Veterans with chronic stroke.} It has two specific aims. Aim 1 will identify EEG features that correlate will the size of the H-reflex in the arm muscle flexor carpi radialis (FCR) and incorporate these features into the operant conditioning protocol. Based on human and animal data, we expect that the best feature will be sensorimotor rhythm (SMR) amplitude over contralateral sensorimotor cortex (SMC) in the 1 sec immediately before H-reflex elicitation. The new protocol will require that this EEG feature satisfy a size criterion prior to H-reflex elicitation. We expect that this new requirement will guide the person to produce, maximize, and maintain appropriate change in corticospinal influence on the reflex pathway; it will thereby increase the reliability, magnitude, and speed of H-reflex change. We will develop and validate this new protocol through studies in Veterans without neurological disease. {Aim 2 will recruit Veterans with impaired arm function due to a stroke >1 yr earlier. One group will undergo FCR H-reflex down-conditioning with the enhanced protocol; another group will undergo down- conditioning with the standard protocol. (We will down-condition the FCR H-reflex in these Veterans because it is the down-conditioning protocol that would be used clinically to reduce the hyperreflexia and/or the abnormal flexor synergy than can occur with stroke.) Because the enhanced protocol will guide the person to produce, maximize, and maintain appropriate change in corticospinal influence on the reflex pathway, we expect that its reliability will be higher, and that it will decrease the H-reflex more and more rapidly, than the standard protocol. This result will validate the enhanced protocol for people with chronic stroke.} In sum, the goal of this project is to gain new mechanistic understanding of a novel therapy and to use this knowledge to improve the therapy. {By identifying an EEG feature that reflects the cortical activity that drives the spinal plasticity underlying H-reflex change, and by showing that the feature can be used to increase the rate, magnitude, and reliability of H-reflex change in Veterans with chronic stroke, this work should augment the therapeutic value and practicality of spinal reflex conditioning.} If it is successful, it should lead to clinical trials that evaluate the ability of this new non-invasive therapy to enhance functional recovery for Veterans with stroke, spinal cord or brain injury, multiple sclerosis, or other chronic neuromuscular disorders. ! !
脊髓损伤(SCI)、创伤性脑损伤、中风、多发性硬化症和其他慢性疾病 产生异常反射,损害运动、伸展和抓取以及其他运动功能 美国人,包括许多退伍军人。迫切需要新的治疗方法。可操作的条件调节方案可以 改变大鼠、小鼠、猴子和人的脊椎反射。这些协议是非侵入性的 人类可以将有益的可塑性作用于特定的反射途径。反射被引出,主题是 如果反射满足大小标准,则给予奖励。受试者学习修改皮质脊髓对 路径。这种控制逐渐改变了脊髓通路本身,从而触发了进一步的有益 其他地方的可塑性。在不完全脊髓损伤患者中,比目鱼肌H反射的可操作性条件反射增加 加快行走速度,减少跛行。这种改善持续存在,在人们的日常生活中是显而易见的。 {患有脊髓损伤或中风的人现在需要在12周内进行36次1小时的反射训练,并且 只有50%-70%是成功的。}更好地理解驱动反射变化的皮质活动应该 导致更好的方案,增加反射条件反射的可靠性、幅度和速度,从而 提升其临床应用价值。该项目致力于识别脑电(EEG)特征,以反映 关键的皮质活动,使用这些功能来改进反射条件调节方案,{并表明这一点 该方案对患有慢性中风的退伍军人有效。}它有两个具体目标。 目标1将确定与手臂腕屈肌H反射大小相关的脑电特征 RADILAIS(FCR),并将这些功能纳入可操作条件反射方案。以人为本, 动物数据,我们预计最好的特征将是感觉运动节律(SMR)的幅度高于对侧 感觉运动皮质(SMC)在紧接H反射刺激前1秒。新的协议将需要 这种脑电特征满足H反射诱发之前的大小标准。我们预计这一新要求 将引导患者产生、最大化并保持皮质脊髓对 反射途径;因此,它将增加H反射变化的可靠性、幅度和速度。我们将发展 并通过对没有神经系统疾病的退伍军人的研究来验证这一新方案。 {Aim 2将招募一年前因中风而手臂功能受损的退伍军人。有一组人会 接受增强方案的FCR H反射下行条件;另一组将接受下行- 使用标准方案进行条件反射。(我们将降低这些退伍军人的FCR H反射,因为它 是临床上用来减少反射亢进和/或异常的下行调节方案 屈肌的协同作用比中风更明显。)因为增强的协议将引导该人产生, 最大化并保持皮质脊髓对反射通路的影响的适当变化,我们预计其 可靠性会更高,而且它会比标准更快地减少H反射 协议。这一结果将验证针对慢性中风患者的增强方案。 总而言之,该项目的目标是获得对一种新疗法的新机制的理解,并使用 这方面的知识有助于提高治疗效果。{通过识别反映大脑皮质活动的脑电特征 驱动H反射变化下的脊柱可塑性,并通过显示这一特征可用于增加 慢性卒中退伍军人H反射改变的速度、幅度和可靠性,这项工作应该 增加脊髓反射训练的治疗价值和实用性。}如果它成功,它应该会导致 评估这种新的非侵入性疗法促进患者功能恢复能力的临床试验 患有中风、脊髓或脑损伤、多发性硬化症或其他慢性神经肌肉疾病的退伍军人。好了! 好了!

项目成果

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Jonathan Rickel Wolpaw其他文献

Jonathan Rickel Wolpaw的其他文献

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{{ truncateString('Jonathan Rickel Wolpaw', 18)}}的其他基金

Corticospinal control of spinal reflex plasticity
皮质脊髓对脊髓反射可塑性的控制
  • 批准号:
    10670047
  • 财政年份:
    2018
  • 资助金额:
    --
  • 项目类别:
Dynamics and Causal Functions of Large-Scale Cortical and Subcortical Networks
大规模皮层和皮层下网络的动力学和因果函数
  • 批准号:
    9789700
  • 财政年份:
    2018
  • 资助金额:
    --
  • 项目类别:
Corticospinal control of spinal reflex plasticity
皮质脊髓对脊髓反射可塑性的控制
  • 批准号:
    10041767
  • 财政年份:
    2018
  • 资助金额:
    --
  • 项目类别:
Center for Adaptive Neurotechnologies
自适应神经技术中心
  • 批准号:
    8742704
  • 财政年份:
    2014
  • 资助金额:
    --
  • 项目类别:
Center for Adaptive Neurotechnologies
自适应神经技术中心
  • 批准号:
    10456334
  • 财政年份:
    2014
  • 资助金额:
    --
  • 项目类别:
Technology Research and Development Project 1 (Guiding Beneficial Plasticity)
技术研发项目1(引导有益可塑性)
  • 批准号:
    10456336
  • 财政年份:
    2014
  • 资助金额:
    --
  • 项目类别:
Operant Conditioning of Spinal Reflexes to Improve Function after Nerve Injury
脊髓反射的操作性调节以改善神经损伤后的功能
  • 批准号:
    8729102
  • 财政年份:
    2014
  • 资助金额:
    --
  • 项目类别:
Center for Adaptive Neurotechnologies
自适应神经技术中心
  • 批准号:
    10239062
  • 财政年份:
    2014
  • 资助金额:
    --
  • 项目类别:
Center for Adaptive Neurotechnologies
自适应神经技术中心
  • 批准号:
    9803919
  • 财政年份:
    2014
  • 资助金额:
    --
  • 项目类别:
Administration
行政
  • 批准号:
    10017987
  • 财政年份:
    2014
  • 资助金额:
    --
  • 项目类别:

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