Tan Andrew Q, Shemmell Jon, Dhaher Yasin Y
Northwestern University Interdepartmental Neuroscience, Northwestern University, Chicago, IL, USA; Sensory Motor Performance Program, Rehabilitation Institute of Chicago, Chicago, IL, USA.
School of Physical Education, Sport and Exercise Science, University of Otago, Dunedin, New Zealand.
Brain Stimul. 2016 May-Jun;9(3):396-405. doi: 10.1016/j.brs.2015.12.006. Epub 2016 Feb 1.
Growing evidence demonstrates unique synergistic signatures in the lower limb (LL) post-stroke, with specific across-plane and across-joint representations. While the inhibitory role of the ipsilateral hemisphere in the upper limb (UL) has been widely reported, examination of the contralesional hemisphere (CON-H) in modulating LL expressions of synergies following stroke is lacking.
We hypothesize that stimulation of lesioned and contralesional motor cortices will differentially regulate paretic LL motor outflow. We propose a novel TMS paradigm to identify synergistic motor evoked potential (MEP) patterns across multiple muscles.
Amplitude and background activation matched adductor MEPs were elicited using single pulse TMS of L-H and CON-H (control ipsilateral) during an adductor torque matching task from 11 stroke and 10 control participants. Associated MEPs of key synergistic muscles were simultaneously observed.
By quantifying CON-H/L-H MEP ratios, we characterized a significant targeted inhibition of aberrant MEP coupling between ADD and VM (p = 0.0078) and VL (p = 0.047) exclusive to the stroke group (p = 0.028) that was muscle dependent (p = 0.039). We find TA inhibition in both groups following ipsilateral hemisphere stimulation (p = 0.0014; p = 0.015).
We argue that ipsilaterally mediated attenuation of abnormal synergistic activations post stroke may reflect an adaptive intracortical inhibition. The predominance of sub 3ms interhemispheric MEP latency differences implicates LL ipsilateral corticomotor projections. These findings provide insight into the association between CON-H reorganization and post-stroke LL recovery. While a prevailing view of driving L-H disinhibition for UL recovery seems expedient, presuming analogous LL neuromodulation may require further examination for rehabilitation. This study provides a step toward this goal.
越来越多的证据表明,中风后下肢(LL)存在独特的协同特征,具有特定的跨平面和跨关节表现。虽然同侧半球在上肢(UL)中的抑制作用已被广泛报道,但缺乏对中风后对侧半球(CON-H)调节LL协同运动表达的研究。
我们假设刺激损伤侧和对侧运动皮层将差异调节患侧LL运动输出。我们提出一种新颖的经颅磁刺激(TMS)范式来识别多块肌肉的协同运动诱发电位(MEP)模式。
在11名中风患者和10名对照参与者进行内收肌扭矩匹配任务期间,使用L-H和CON-H(对照同侧)的单脉冲TMS引出振幅和背景激活匹配的内收肌MEP。同时观察关键协同肌肉的相关MEP。
通过量化CON-H/L-H MEP比率,我们发现中风组(p = 0.028)特有的ADD与VM(p = 0.0078)和VL(p = 0.047)之间异常MEP耦合的显著靶向抑制,且这种抑制是肌肉依赖性的(p = 0.039)。我们发现同侧半球刺激后两组的TA均受到抑制(p = 0.0014;p = 0.015)。
我们认为,中风后同侧介导的异常协同激活的减弱可能反映了一种适应性皮质内抑制。半球间MEP潜伏期差异小于3ms占优势,这暗示了LL同侧皮质运动投射。这些发现为CON-H重组与中风后LL恢复之间的关联提供了见解。虽然促进UL恢复的L-H去抑制的主流观点似乎很便利,但假设类似的LL神经调节可能需要进一步研究以用于康复。本研究朝着这一目标迈出了一步。