Sobell Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, University College London, London, United Kingdom.
J Neurosci. 2010 Sep 8;30(36):11926-37. doi: 10.1523/JNEUROSCI.5642-09.2010.
Contralesional dorsal premotor cortex (cPMd) may support residual motor function following stroke. We performed two complementary experiments to explore how cPMd might perform this role in a group of chronic human stroke patients. First, we used paired-coil transcranial magnetic stimulation (TMS) to establish the physiological influence of cPMd on ipsilesional primary motor cortex (iM1) at rest. We found that this influence became less inhibitory/more facilitatory in patients with greater clinical impairment. Second, we applied TMS over cPMd during functional magnetic resonance imaging (fMRI) in these patients to examine the causal influence of cPMd TMS on the whole network of surviving cortical motor areas in either hemisphere and whether these influences changed during affected hand movement. We confirmed that hand grip-related activation in cPMd was greater in more impaired patients. Furthermore, the peak ipsilesional sensorimotor cortex activity shifted posteriorly in more impaired patients. Critical new findings were that concurrent TMS-fMRI results correlated with the level of both clinical impairment and neurophysiological impairment (i.e., less inhibitory/more facilitatory cPMd-iM1 measure at rest as assessed with paired-coil TMS). Specifically, greater clinical and neurophysiological impairment was associated with a stronger facilitatory influence of cPMd TMS on blood oxygenation level-dependent signal in posterior parts of ipsilesional sensorimotor cortex during hand grip, corresponding to the posteriorly shifted sensorimotor activity seen in more impaired patients. cPMd TMS was not found to influence activity in other brain regions in either hemisphere. This state-dependent influence on ipsilesional sensorimotor regions may provide a mechanism by which cPMd supports recovered function after stroke.
对侧背侧运动前皮质(cPMd)可能在中风后支持残留的运动功能。我们进行了两项互补实验,以探索 cPMd 如何在一组慢性中风患者中发挥此作用。首先,我们使用双线圈经颅磁刺激(TMS)来确定 cPMd 在静息状态下对同侧初级运动皮质(iM1)的生理影响。我们发现,这种影响在临床损伤较大的患者中变得抑制作用较小/促进作用较大。其次,我们在这些患者的功能磁共振成像(fMRI)期间应用 TMS 刺激 cPMd,以检查 cPMd TMS 对任一半球中幸存的皮质运动区域的整个网络的因果影响,以及这些影响是否在手受影响运动期间发生变化。我们证实,cPMd 与手抓握相关的激活在损伤更严重的患者中更高。此外,在损伤更严重的患者中,同侧感觉运动皮质的峰值活动向后移位。新的关键发现是,同时进行的 TMS-fMRI 结果与临床损伤和神经生理损伤的程度都相关(即,使用双线圈 TMS 评估时,静息时 cPMd-iM1 的抑制作用减少/促进作用增加)。具体而言,更大的临床和神经生理损伤与 cPMd TMS 在抓握期间对同侧感觉运动皮质后部血氧水平依赖信号的更强促进作用相关,这与损伤更严重的患者中可见的感觉运动活动向后移位相对应。未发现 cPMd TMS 影响大脑半球其他区域的活动。这种对同侧感觉运动区域的状态依赖性影响可能为 cPMd 在中风后支持恢复功能提供了一种机制。