Short-interval and long-interval intracortical inhibition of TMS-evoked EEG potentials

100奈拉 刺激间期 磁刺激 神经科学 巴氯芬 诱发电位 γ-氨基丁酸受体 γ-氨基丁酸受体 心理学 脑电图 化学 医学 刺激 兴奋剂 受体 事件相关电位 内科学
作者
Isabella Premoli,Julia Király,Florian Müller‐Dahlhaus,Carl Moritz Zipser,Pierre Gilbert Rossini,Christoph Zrenner,Ulf Ziemann,Paolo Belardinelli
出处
期刊:Brain Stimulation [Elsevier BV]
卷期号:11 (4): 818-827 被引量:63
标识
DOI:10.1016/j.brs.2018.03.008
摘要

Inhibition in the human motor cortex can be probed by means of paired-pulse transcranial magnetic stimulation (ppTMS) at interstimulus intervals of 2-3 ms (short-interval intracortical inhibition, SICI) or ∼100 ms (long-interval intracortical inhibition, LICI). Conventionally, SICI and LICI are recorded as motor evoked potential (MEP) inhibition in the hand muscle. Pharmacological experiments indicate that they are mediated by GABAA and GABAB receptors, respectively.SICI and LICI of TMS-evoked EEG potentials (TEPs) and their pharmacological properties have not been systematically studied. Here, we sought to examine SICI by ppTMS-evoked compared to single-pulse TMS-evoked TEPs, to investigate its pharmacological manipulation and to compare SICI with our previous results on LICI.PpTMS-EEG was applied to the left motor cortex in 16 healthy subjects in a randomized, double-blind placebo-controlled crossover design, testing the effects of a single oral dose 20 mg of diazepam, a positive modulator at the GABAA receptor, vs. 50 mg of the GABAB receptor agonist baclofen on SICI of TEPs.We found significant SICI of the N100 and P180 TEPs prior to drug intake. Diazepam reduced SICI of the N100 TEP, while baclofen enhanced it. Compared to our previous ppTMS-EEG results on LICI, the SICI effects on TEPs, including their drug modulation, were largely analogous.Findings suggest a similar interaction of paired-pulse effects on TEPs irrespective of the interstimulus interval. Therefore, SICI and LICI as measured with TEPs cannot be directly derived from SICI and LICI measured with MEPs, but may offer novel insight into paired-pulse responses recorded directly from the brain rather than muscle.
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