人类运动皮层和脊髓后部刺激之间的时间依赖性协同作用。

James R McIntosh, Evan F Joiner, Jacob L Goldberg, Phoebe Greenwald, Lynda M Murray, Earl Thuet, Oleg Modik, Evgeny Shelkov, Joseph M Lombardi, Zeeshan M Sardar, Ronald A Lehman, Andrew K Chan, K Daniel Riew, Noam Y Harel, Michael S Virk, Christopher Mandigo, Jason B Carmel
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引用次数: 0

摘要

电刺激大脑和脊髓可以加强感觉运动回路,并通过联想可塑性改善运动。目前的成对刺激模式仅针对皮层中的运动系统或感觉运动连接。我们在大鼠身上开发了一种针对颈脊髓感觉和运动连接的配对刺激方法。由于配对刺激所需的回路在物种之间是保守的,我们假设人类对运动皮层和颈后脊髓的配对刺激会产生协同的肌肉反应,但只有在刺激时机合适的情况下。在59名接受临床指示的颈椎手术的患者中,用头皮电极刺激运动皮层,用硬膜外电极刺激脊髓,同时记录手臂和腿部肌肉的肌肉反应。脊髓电极放置在脊髓后部或前部,皮层和脊髓刺激之间的间隔是不同的。运动皮层和脊髓后部(而不是前部)之间的配对刺激产生的运动诱发电位是单独大脑刺激的五倍多。当下行运动和脊髓传入刺激定时汇聚在颈脊髓时,就会出现这种强烈的增强。相对于未配对的大脑或脊髓刺激,配对刺激还增加了肌肉反应的选择性。最后,通过临床体征或脊髓成像测量,无论脊髓病的严重程度如何,都会出现配对刺激效应。这种配对刺激的大效应大小使其成为治疗神经调控的有前途的候选。
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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Timing dependent synergies between motor cortex and posterior spinal stimulation in humans.

Volitional movement requires descending input from motor cortex and sensory feedback through the spinal cord. We previously developed a paired brain and spinal electrical stimulation approach in rats that relies on convergence of the descending motor and spinal sensory stimuli in the cervical cord. This approach strengthened sensorimotor circuits and improved volitional movement through associative plasticity. In humans it is not known whether dorsal epidural SCS targeted at the sensorimotor interface or anterior epidural SCS targeted within the motor system is effective at facilitating brain evoked responses. In 59 individuals undergoing elective cervical spine decompression surgery, the motor cortex was stimulated with scalp electrodes and the spinal cord with epidural electrodes while muscle responses were recorded in arm and leg muscles. Spinal electrodes were placed either posteriorly or anteriorly, and the interval between cortex and spinal cord stimulation was varied. Pairing stimulation between the motor cortex and spinal sensory (posterior) but not spinal motor (anterior) stimulation produced motor evoked potentials that were over five times larger than brain stimulation alone. This strong augmentation occurred only when descending motor and spinal afferent stimuli were timed to converge in the spinal cord. Paired stimulation also increased the selectivity of muscle responses relative to unpaired brain or spinal cord stimulation. Finally, paired stimulation effects were present regardless of the severity of myelopathy as measured by clinical signs or spinal cord imaging. The large effect size of this paired stimulation makes it a promising candidate for therapeutic neuromodulation.

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