Neurophysiological Basis for Enhancing Motor Recovery After Stroke

增强中风后运动恢复的神经生理学基础

基本信息

项目摘要

Stroke is a major cause of disability in veterans. Despite significant advances in stroke rehabilitation methods there continue to be substantial long-term disability. Importantly, quantitative assessments have found that a major contributor to motor impairments is the presence of fragmented movement control, characterized by a lack of smooth and fast transitions between sub-movements and inconsistency over multiple attempts. Furthermore, there is a deficit in learning new movement sequences. It remains unclear what is the precise circuit basis for such deficits. The central hypothesis of this proposal is that impaired task-dependent recruitment of the striatum contributes to fragmented movement control and poor learning. There has been a great focus on the role of perilesional cortex (PLC) in recovery. In the intact brain, however, cortical areas work in close concert with subcortical regions; interactions between M1 and the dorsolateral striatum (DLS) are known to play a critical role in learning and generating smooth and consistent skilled movements. Little is known about how the DLS might contribute to motor recovery after stroke. Our preliminary data shows that coordination between M1 and DLS is directly linked to “binding” of movement fragments to result in a smooth and fast skilled action. We further found that DLS is essential for such execution; inhibition of DLS increased movement fragmentation. Our data also demonstrates that DLS activity is affected by stroke and that its activity changes with recovery. We propose to pursue the following specific aims: 1) Determine the role of task-related oscillatory activity in the DLS in regulating movement fragmentation during spontaneous motor recovery after cortical stroke; 2) Determine the role of low-frequency coherence between areas during spontaneous recovery in the setting of a stroke that involves both cortex and striatum; 3) Determine if paired stimulation can increase coordination and thereby improve motor outcomes. Completion of these aims will provide critical information for designing therapeutic approaches that specifically target cortico-striatal activity. Focusing on targeted neuromodulation of such dynamic neural network interactions represents a new direction that could transform our ability to augment recovery of upper extremity function following stroke.
中风是退伍军人残疾的主要原因。尽管中风康复取得了重大进展 方法仍然存在严重的长期残疾。重要的是,定量评估 发现运动障碍的一个主要原因是零碎运动的存在 控制,其特点是子运动和子运动之间缺乏平滑和快速的过渡 多次尝试不一致。此外,在学习新动作方面存在缺陷 序列。目前尚不清楚这种缺陷的确切电路基础是什么。 该提案的中心假设是,任务依赖性招募受损 纹状体导致运动控制分散和学习不良。曾经有过一次伟大的 重点关注病灶周围皮层 (PLC) 在恢复中的作用。然而,在完整的大脑中,皮质区域 与皮质下区域密切配合; M1 和背外侧纹状体之间的相互作用 众所周知,DLS 在学习和培养平稳一致的技能方面发挥着关键作用 动作。人们对 DLS 如何促进中风后运动恢复知之甚少。我们的 初步数据显示,M1和DLS之间的协调与运动的“束缚”直接相关 片段以产生平稳快速的熟练动作。我们进一步发现 DLS 对于这种情况至关重要 执行;抑制 DLS 会增加运动碎片化。我们的数据还表明,DLS 活动受到中风的影响,并且其活动随着恢复而变化。 我们建议追求以下具体目标:1)确定任务相关振荡活动的作用 DLS 在皮质后自发运动恢复过程中调节运动碎片 中风; 2)确定自发恢复过程中区域之间低频相干性的作用 在涉及皮质和纹状体的中风的情况下; 3)确定配对刺激是否可以 增强协调性,从而改善运动效果。完成这些目标将提供 设计专门针对皮质纹状体活动的治疗方法的关键信息。 关注这种动态神经网络交互的有针对性的神经调节代表了一种新的方法 这个方向可以改变我们增强中风后上肢功能恢复的能力。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

Karunesh Ganguly其他文献

Karunesh Ganguly的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('Karunesh Ganguly', 18)}}的其他基金

Detecting Movement Onset During Closed-Loop Stimulation Using A Hidden Markov Model.
使用隐马尔可夫模型检测闭环刺激期间的运动起始。
  • 批准号:
    10842105
  • 财政年份:
    2023
  • 资助金额:
    --
  • 项目类别:
Optimizing oscillatory epidural electrical stimulation to selectively increase task-related population dynamics in motor areas
优化振荡硬膜外电刺激以选择性地增加运动区域中与任务相关的群体动态
  • 批准号:
    10267682
  • 财政年份:
    2020
  • 资助金额:
    --
  • 项目类别:
Optimizing oscillatory epidural electrical stimulation to selectively increase task-related population dynamics in motor areas
优化振荡硬膜外电刺激以选择性地增加运动区域中与任务相关的群体动态
  • 批准号:
    10681335
  • 财政年份:
    2020
  • 资助金额:
    --
  • 项目类别:
Modulating Low-Frequency Cortical Population Dynamics to Augment Motor Function After Stroke
调节低频皮质群动态以增强中风后的运动功能
  • 批准号:
    10376037
  • 财政年份:
    2020
  • 资助金额:
    --
  • 项目类别:
Optimizing oscillatory epidural electrical stimulation to selectively increase task-related population dynamics in motor areas
优化振荡硬膜外电刺激以选择性地增加运动区域中与任务相关的群体动态
  • 批准号:
    10468122
  • 财政年份:
    2020
  • 资助金额:
    --
  • 项目类别:
Optimizing oscillatory epidural electrical stimulation to selectively increase task-related population dynamics in motor areas
优化振荡硬膜外电刺激以选择性地增加运动区域中与任务相关的群体动态
  • 批准号:
    10031331
  • 财政年份:
    2020
  • 资助金额:
    --
  • 项目类别:
Modulating Low-Frequency Cortical Population Dynamics to Augment Motor Function After Stroke
调节低频皮质群动态以增强中风后的运动功能
  • 批准号:
    10602448
  • 财政年份:
    2020
  • 资助金额:
    --
  • 项目类别:
ShEEP request for an Inscopix nVoke Integrated Imaging and Optogenetics System
ShEEP 请求 Inscopix nVoke 集成成像和光遗传学系统
  • 批准号:
    9795729
  • 财政年份:
    2019
  • 资助金额:
    --
  • 项目类别:
Optimizing peripheral stimulation parameters to modulate the sensorimotor cortex for post-stroke motor recovery
优化外周刺激参数以调节感觉运动皮层以实现中风后运动恢复
  • 批准号:
    9229152
  • 财政年份:
    2016
  • 资助金额:
    --
  • 项目类别:
Neurophysiological Basis for Enhancing Motor Recovery After Stroke
增强中风后运动恢复的神经生理学基础
  • 批准号:
    10385691
  • 财政年份:
    2015
  • 资助金额:
    --
  • 项目类别:

相似海外基金

The earliest exploration of land by animals: from trace fossils to numerical analyses
动物对陆地的最早探索:从痕迹化石到数值分析
  • 批准号:
    EP/Z000920/1
  • 财政年份:
    2025
  • 资助金额:
    --
  • 项目类别:
    Fellowship
Animals and geopolitics in South Asian borderlands
南亚边境地区的动物和地缘政治
  • 批准号:
    FT230100276
  • 财政年份:
    2024
  • 资助金额:
    --
  • 项目类别:
    ARC Future Fellowships
The function of the RNA methylome in animals
RNA甲基化组在动物中的功能
  • 批准号:
    MR/X024261/1
  • 财政年份:
    2024
  • 资助金额:
    --
  • 项目类别:
    Fellowship
Ecological and phylogenomic insights into infectious diseases in animals
对动物传染病的生态学和系统发育学见解
  • 批准号:
    DE240100388
  • 财政年份:
    2024
  • 资助金额:
    --
  • 项目类别:
    Discovery Early Career Researcher Award
Zootropolis: Multi-species archaeological, ecological and historical approaches to animals in Medieval urban Scotland
Zootropolis:苏格兰中世纪城市动物的多物种考古、生态和历史方法
  • 批准号:
    2889694
  • 财政年份:
    2023
  • 资助金额:
    --
  • 项目类别:
    Studentship
Using novel modelling approaches to investigate the evolution of symmetry in early animals.
使用新颖的建模方法来研究早期动物的对称性进化。
  • 批准号:
    2842926
  • 财政年份:
    2023
  • 资助金额:
    --
  • 项目类别:
    Studentship
Study of human late fetal lung tissue and 3D in vitro organoids to replace and reduce animals in lung developmental research
研究人类晚期胎儿肺组织和 3D 体外类器官在肺发育研究中替代和减少动物
  • 批准号:
    NC/X001644/1
  • 财政年份:
    2023
  • 资助金额:
    --
  • 项目类别:
    Training Grant
RUI: Unilateral Lasing in Underwater Animals
RUI:水下动物的单侧激光攻击
  • 批准号:
    2337595
  • 财政年份:
    2023
  • 资助金额:
    --
  • 项目类别:
    Continuing Grant
RUI:OSIB:The effects of high disease risk on uninfected animals
RUI:OSIB:高疾病风险对未感染动物的影响
  • 批准号:
    2232190
  • 财政年份:
    2023
  • 资助金额:
    --
  • 项目类别:
    Continuing Grant
A method for identifying taxonomy of plants and animals in metagenomic samples
一种识别宏基因组样本中植物和动物分类的方法
  • 批准号:
    23K17514
  • 财政年份:
    2023
  • 资助金额:
    --
  • 项目类别:
    Grant-in-Aid for Challenging Research (Exploratory)
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了