Fleischmann Robert, Triller Paul, Brandt Stephan A, Schmidt Sein H
Vision and Motor System Research Group, Department of Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Department of Neurology, University Medicine Greifswald, Greifswald, Germany.
Front Neuroergon. 2021 May 19;2:678906. doi: 10.3389/fnrgo.2021.678906. eCollection 2021.
The significance of pre-motor (PMC) corticospinal projections in a frontoparietal motor network remains elusive. Temporal activation patterns can provide valuable information about a region's engagement in a hierarchical network. Navigated transcranial magnetic stimulation (nTMS)-induced virtual lesions provide an excellent method to study cortical physiology by disrupting ongoing activity at high temporal resolution and anatomical precision. We use nTMS-induced virtual lesions applied during an established behavioral task demanding pre-motor activation to clarify the temporal activation pattern of pre-motor corticospinal projections. Ten healthy volunteers participated in the experiment (4 female, mean age 24 ± 2 years, 1 left-handed). NTMS was used to map Brodmann areae 4 and 6 for primary motor (M1) and PMC corticospinal projections. We then determined the stimulator output intensity required to elicit a 1 mV motor evoked potential (1 mV-MT) through M1 nTMS. TMS pulse were randomly delivered at distinct time intervals (40, 60, 80, 100, 120, and 140 ms) at 1 mV-MT intensity to M1, PMC and the DLPFC (dorsolateral pre-frontal cortex; control condition) before participants had to perform major changes of their trajectory of movement during a tracing task. Each participant performed six trials (20 runs per trial). Task performance and contribution of regions under investigation was quantified through calculating the tracing error induced by the stimulation. A pre-motor stimulation hotspot could be identified in all participants (16.3 ± 1.7 mm medial, 18.6 ± 1.4 mm anterior to the M1 hotspot). NTMS over studied regions significantly affected task performance at discrete time intervals ( = 3.25, = 0.001). NTMS applied over PMC 120 and 140 ms before changes in movement trajectory impaired task performance significantly more than when applied over M1 ( = 0.021 and = 0.003) or DLPFC ( = 0.017 and < 0.001). Stimulation intensity did not account for error size ( = -0.0074, = 1). We provide novel evidence that the role of pre-motor corticospinal projections extends beyond that of simple corticospinal motor output. Their activation is crucial for task performance early in the stage of motor preparation suggesting a significant role in shaping voluntary movement. Temporal patterns of human pre-motor activation are similar to that observed in intracortical electrophysiological studies in primates.
前额叶顶叶运动网络中运动前区(PMC)皮质脊髓投射的意义仍不清楚。时间激活模式可以提供有关一个区域在层级网络中参与情况的有价值信息。导航经颅磁刺激(nTMS)诱导的虚拟损伤提供了一种通过在高时间分辨率和解剖精度下破坏正在进行的活动来研究皮质生理学的出色方法。我们使用在一项需要运动前区激活的既定行为任务期间施加的nTMS诱导虚拟损伤,以阐明运动前区皮质脊髓投射的时间激活模式。10名健康志愿者参与了实验(4名女性,平均年龄24±2岁,1名左利手)。使用nTMS来绘制初级运动区(M1)和PMC皮质脊髓投射的布罗德曼4区和6区。然后我们通过M1 nTMS确定诱发1 mV运动诱发电位(1 mV-MT)所需的刺激器输出强度。在参与者必须在追踪任务期间对其运动轨迹进行重大改变之前,以1 mV-MT强度在不同时间间隔(40、60、80、100、120和140 ms)将TMS脉冲随机施加到M1、PMC和背外侧前额叶皮质(DLPFC;对照条件)。每位参与者进行6次试验(每次试验20次运行)。通过计算刺激引起的追踪误差来量化任务表现和所研究区域的贡献。在所有参与者中都可以识别出一个运动前区刺激热点(在M1热点内侧16.3±1.7 mm,前方18.6±1.4 mm)。在研究区域进行的nTMS在离散时间间隔显著影响任务表现(F = 3.25,p = 0.001)。在运动轨迹改变前120和140 ms对PMC施加nTMS比在M1(p = 0.021和p = 0.003)或DLPFC(p = 0.017和p < 0.001)施加时更显著地损害任务表现。刺激强度与误差大小无关(r = -0.0074,p = 1)。我们提供了新的证据,表明运动前区皮质脊髓投射的作用超出了简单的皮质脊髓运动输出。它们的激活对于运动准备阶段早期的任务表现至关重要,这表明在塑造自主运动中起重要作用。人类运动前区激活的时间模式与在灵长类动物的皮质内电生理研究中观察到的相似。