Center for Pain IMPACT, Neuroscience Research Australia, Sydney, Australia.
University of New South Wales, Sydney, Australia.
Elife. 2023 Nov 15;12:RP88567. doi: 10.7554/eLife.88567.
Transcranial magnetic stimulation (TMS) has been used to examine inhibitory and facilitatory circuits during experimental pain and in chronic pain populations. However, current applications of TMS to pain have been restricted to measurements of motor evoked potentials (MEPs) from peripheral muscles. Here, TMS was combined with electroencephalography (EEG) to determine whether experimental pain could induce alterations in cortical inhibitory/facilitatory activity observed in TMS-evoked potentials (TEPs). In Experiment 1 (n=29), multiple sustained thermal stimuli were administered to the forearm, with the first, second, and third block of thermal stimuli consisting of warm but non-painful (pre-pain block), painful (pain block) and warm but non-painful (post-pain block) temperatures, respectively. During each stimulus, TMS pulses were delivered while EEG (64 channels) was simultaneously recorded. Verbal pain ratings were collected between TMS pulses. Relative to pre-pain warm stimuli, painful stimuli led to an increase in the amplitude of the frontocentral negative peak ~45 ms post-TMS (N45), with a larger increase associated with higher pain ratings. Experiments 2 and 3 (n=10 in each) showed that the increase in the N45 in response to pain was not due to changes in sensory potentials associated with TMS, or a result of stronger reafferent muscle feedback during pain. This is the first study to use combined TMS-EEG to examine alterations in cortical excitability in response to pain. These results suggest that the N45 TEP peak, which indexes GABAergic neurotransmission, is implicated in pain perception and is a potential marker of individual differences in pain sensitivity.
经颅磁刺激(TMS)已被用于研究实验性疼痛和慢性疼痛人群中的抑制和易化回路。然而,目前 TMS 在疼痛中的应用仅限于外周肌肉运动诱发电位(MEPs)的测量。在这里,TMS 与脑电图(EEG)相结合,以确定实验性疼痛是否会引起 TMS 诱发电位(TEPs)中观察到的皮质抑制/易化活性的改变。在实验 1(n=29)中,在前臂上给予多次持续的热刺激,第一、第二和第三组热刺激分别由温暖但无痛(预痛组)、疼痛(痛组)和温暖但无痛(痛后组)组成。在每个刺激期间,当 EEG(64 个通道)同时记录时,会给予 TMS 脉冲。在 TMS 脉冲之间收集言语疼痛评分。与预痛温暖刺激相比,疼痛刺激导致 TMS 后约 45 毫秒时额中央负峰(N45)的振幅增加,与更高的疼痛评分相关的增加更大。实验 2 和 3(每组 n=10)表明,对疼痛的 N45 增加不是由于与 TMS 相关的感觉电位的变化,也不是由于疼痛期间更强的传入肌肉反馈所致。这是首次使用 TMS-EEG 联合研究皮质兴奋性对疼痛的反应变化。这些结果表明,N45 TEP 峰值,其指数 GABA 能神经传递,与疼痛感知有关,是个体疼痛敏感性差异的潜在标志物。