Brain, Mind and Society Research Hub, School of Psychological Sciences and Turner Institute for Brain and Mental Health, Monash University, Melbourne, Australia.
Hopwood Centre for Neurobiology, Lifelong Health Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, Australia.
Sci Rep. 2020 Feb 21;10(1):3168. doi: 10.1038/s41598-020-59911-6.
Measuring the brain's response to transcranial magnetic stimulation (TMS) with electroencephalography (EEG) offers unique insights into the cortical circuits activated following stimulation, particularly in non-motor regions where less is known about TMS physiology. However, the mechanisms underlying TMS-evoked EEG potentials (TEPs) remain largely unknown. We assessed TEP sensitivity to changes in excitatory neurotransmission mediated by n-methyl-d-aspartate (NMDA) receptors following stimulation of non-motor regions. In fourteen male volunteers, resting EEG and TEPs from prefrontal (PFC) and parietal (PAR) cortex were measured before and after administration of either dextromethorphan (NMDA receptor antagonist) or placebo across two sessions in a double-blinded pseudo-randomised crossover design. At baseline, there were amplitude differences between PFC and PAR TEPs across a wide time range (15-250 ms), however the signals were correlated after ~80 ms, suggesting early peaks reflect site-specific activity, whereas late peaks reflect activity patterns less dependent on the stimulated sites. Early TEP peaks were not reliably altered following dextromethorphan compared to placebo, although findings were less clear for later peaks, and low frequency resting oscillations were reduced in power. Our findings suggest that early TEP peaks (<80 ms) from PFC and PAR reflect stimulation site specific activity that is largely insensitive to changes in NMDA receptor-mediated neurotransmission.
使用脑电图 (EEG) 测量经颅磁刺激 (TMS) 对大脑的反应,为皮层回路在刺激后的激活提供了独特的见解,特别是在对 TMS 生理学了解较少的非运动区域。然而,TMS 诱发的脑电图电位 (TEP) 的机制在很大程度上仍然未知。我们评估了 TEP 对非运动区域刺激后兴奋性神经递质传递介导的 N-甲基-D-天冬氨酸 (NMDA) 受体变化的敏感性。在十四名男性志愿者中,在双盲伪随机交叉设计的两个会话中,在给予右美沙芬(NMDA 受体拮抗剂)或安慰剂前后,分别测量前额叶 (PFC) 和顶叶 (PAR) 皮层的静息 EEG 和 TEP。在基线时,PFC 和 PAR TEP 在广泛的时间范围内存在幅度差异(15-250ms),但在~80ms 后信号相关,表明早期峰值反映了特定部位的活动,而晚期峰值反映了对刺激部位依赖性较小的活动模式。与安慰剂相比,右美沙芬后早期 TEP 峰值(<80ms)与安慰剂相比没有可靠改变,尽管晚期峰值的发现不太清楚,低频静息振荡的功率降低。我们的发现表明,来自 PFC 和 PAR 的早期 TEP 峰值 (<80ms) 反映了刺激部位特异性活动,而 NMDA 受体介导的神经递质传递变化对其影响不大。