State dependent motor cortex stimulation reveals distinct mechanisms for corticospinal excitability and cortical responses.

IF 2.7 3区 医学 Q3 NEUROSCIENCES eNeuro Pub Date : 2024-11-14 DOI:10.1523/ENEURO.0450-24.2024
Nipun D Perera, Miles Wischnewski, Ivan Alekseichuk, Sina Shirinpour, Alexander Opitz
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Abstract

Transcranial magnetic stimulation (TMS) is a non-invasive brain stimulation method that modulates brain activity by inducing electric fields in the brain. Real-time, state-dependent stimulation with TMS has shown that neural oscillation phase modulates corticospinal excitability. However, such motor-evoked potentials (MEPs) only indirectly reflect motor cortex activation and are unavailable at other brain regions of interest. The direct and secondary cortical effects of phase-dependent brain stimulation remain an open question. In this study, we recorded the cortical responses during single-pulse TMS using electroencephalography (EEG) concurrently with the MEP measurements in 20 healthy human volunteers (11 female). TMS was delivered at peak, rising, trough, and falling phases of mu (8-13 Hz) and beta (14-30 Hz) oscillations in the motor cortex. The cortical responses were quantified through TMS-evoked potential components N15, P50, and N100 as peak-to-peak amplitudes (P50-N15 and P50-N100). We further analyzed whether the pre-stimulus frequency band power was predictive of the cortical responses. We demonstrated that phase-specific targeting modulates cortical responses. The phase relationship between cortical responses was different for early and late responses. In addition, pre-TMS mu oscillatory power and phase significantly predicted both early and late cortical EEG responses in mu-specific targeting, indicating the independent causal effects of phase and power. However, only pre-TMS beta power significantly predicted the early and late TEP components during beta-specific targeting. Further analyses indicated distinct roles of mu and beta power on cortical responses. These findings provide insight to mechanistic understanding of neural oscillation states in cortical and corticospinal activation in humans.Significance Statement Understanding the effects of noninvasive neuromodulation on human brain provides valuable insights to its clinical utility. Brain state dependent stimulation helps us understand mechanisms leading to cortical responses and behavioral outcomes. Here we study the effects of the phase of ongoing oscillations in the motor cortex on cortical responses measured by electroencephalography. We also studied the relationship of phase preference between cortical responses and motor evoked potentials. Furthermore, we investigated the effects of the power of ongoing oscillations on cortical responses. These findings are important to understand the changes in biomarkers during state-dependent brain stimulation and their relationship to behavioral outcomes. At large, this helps the researchers to utilize state-dependent brain stimulation to enhance treatment efficacy.

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与状态相关的运动皮层刺激揭示了皮质脊髓兴奋性和皮层反应的不同机制。
经颅磁刺激(TMS)是一种非侵入性脑部刺激方法,通过在大脑中诱导电场来调节大脑活动。经颅磁刺激的实时、状态依赖性刺激表明,神经振荡相位可调节皮质脊髓的兴奋性。然而,这种运动诱发电位(MEPs)只能间接反映运动皮层的激活情况,而无法反映其他相关脑区的情况。相位依赖性脑刺激对大脑皮层的直接和继发性影响仍是一个未决问题。在这项研究中,我们使用脑电图(EEG)记录了 20 名健康志愿者(11 名女性)在单脉冲 TMS 期间的皮层反应,同时进行了 MEP 测量。TMS 在运动皮层μ(8-13 Hz)和β(14-30 Hz)振荡的高峰、上升、低谷和下降阶段进行。皮层反应通过 TMS 诱发电位成分 N15、P50 和 N100 的峰-峰振幅(P50-N15 和 P50-N100)进行量化。我们进一步分析了刺激前频带功率是否能预测皮层反应。我们证明了相位特异性靶向调节皮层反应。早期和晚期皮层反应的相位关系不同。此外,在μ特异性靶向中,TMS前μ振荡功率和相位可显著预测早期和晚期皮层脑电图反应,这表明相位和功率具有独立的因果效应。然而,只有TMS前β功率能显著预测β特异性靶向的早期和晚期TEP成分。进一步的分析表明,μ和β功率对皮层反应的作用截然不同。这些发现为从机理上理解人类皮质和皮质脊髓激活的神经振荡状态提供了启示。 意义声明 了解非侵入性神经调控对人脑的影响为其临床应用提供了宝贵的见解。与脑状态相关的刺激有助于我们了解导致大脑皮层反应和行为结果的机制。在这里,我们研究了运动皮层持续振荡的相位对脑电图测量的皮层反应的影响。我们还研究了大脑皮层反应与运动诱发电位之间的相位偏好关系。此外,我们还研究了持续振荡的功率对皮层反应的影响。这些发现对于了解状态依赖性脑刺激过程中生物标志物的变化及其与行为结果的关系非常重要。总的来说,这有助于研究人员利用状态依赖性脑刺激提高治疗效果。
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来源期刊
eNeuro
eNeuro Neuroscience-General Neuroscience
CiteScore
5.00
自引率
2.90%
发文量
486
审稿时长
16 weeks
期刊介绍: An open-access journal from the Society for Neuroscience, eNeuro publishes high-quality, broad-based, peer-reviewed research focused solely on the field of neuroscience. eNeuro embodies an emerging scientific vision that offers a new experience for authors and readers, all in support of the Society’s mission to advance understanding of the brain and nervous system.
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