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Transcranial magnetic stimulation (TMS) is a noninvasive 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 prestimulus 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.
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Modulation of cortical beta oscillations influences motor vigor: A rhythmic TMS‐EEG study
Abstract Previous electro‐ or magnetoencephalography (Electro/Magneto EncephaloGraphic; E/MEG) studies using a correlative approach have shown that β (13–30 Hz) oscillations emerging in the primary motor cortex (M1) are implicated in regulating motor response vigor and associated with an anti‐kinetic role, that is, slowness of movement. However, the functional role of M1 β oscillations in regulation of motor responses remains unclear. To address this gap, we combined EEG with rhythmic TMS (rhTMS) delivered to M1 at the β (20 Hz) frequency shortly before subjects performed an isometric ramp‐and‐hold finger force production task at three force levels. rhTMS is a novel approach that can modulate rhythmic patterns of neural activity. β‐rhTMS over M1 induced a modulation of neural oscillations to β frequency in the sensorimotor area and reduced peak force rate during the ramp‐up period relative to sham and catch trials. Interestingly, this rhTMS effect occurred only in the large force production condition. To distinguish whether the effects of rhTMS on EEG and behavior stemmed from phase‐resetting by each magnetic pulse or neural entrainment by the periodicity of rhTMS, we performed a control experiment using arrhythmic TMS (arTMS). arTMS did not induce changes in EEG oscillations nor peak force rate during the rump‐up period. Our results provide novel evidence that β neural oscillations emerging the sensorimotor area influence the regulation of motor response vigor. Furthermore, our findings further demonstrate that rhTMS is a promising tool for tuning neural oscillations to the target frequency.
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- Award ID(s):
- 1827725
- PAR ID:
- 10448675
- Date Published:
- Journal Name:
- Human Brain Mapping
- Volume:
- 44
- Issue:
- 3
- ISSN:
- 1065-9471
- Page Range / eLocation ID:
- 1158 to 1172
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Studying electroencephalography (EEG) in response to transcranial magnetic stimulation (TMS) is gaining popularity for investigating the dynamics of complex neural architecture in the brain. For example, the primary motor cortex (M1) executes voluntary movements by complex connections with other associated subnetworks. To understand these connections better, we analyzed EEG signal response to TMS at left M1 from schizophrenia patients and healthy controls and in contrast with resting state EEG recording. After removing artifacts from EEG, we conducted 2D to 3D sLORETA conversion, a well-established source localization method, for estimating signal strength of 68 source dipoles or cortical regions inside the brain. Next, we studied dynamic connectivity by computing time-evolving spatial coherence of 2278 (=68*(68-1)/2) pairs of cortical regions, with sliding window technique of 200ms window size and 20ms shift over 1sec long data. Pairs with consistent coherence (coherence>0.8 during 200+ sliding windows of patients and controls combined) were chosen for identifying stable networks. For example, we found that during the resting state, precuneus was steadily coherent with middle and superior temporal gyrus in the left hemisphere in both patient and controls. Their connectivity pattern over the sliding windows significantly differed between patients and controls (pvalue<0.05). Whereas for M1, the same was true for two other coherent pairs namely, superamarginal gyrus with lateral occipital gyrus in right hemisphere and medial orbitofrontal gyrus with fusiform in left hemisphere. The TMS-EEG dynamic connectivity results can help to differentiate patient and normal subjects and also help to better understand the brain architecture and mechanisms.more » « less
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Multimodal neuroimaging using electroencephalography (EEG) and functional near-infrared spectroscopy (fNIRS) provides complementary views of cortical processes, including those related to auditory processing. However, current multimodal approaches often overlook potential insights that can be gained from nonlinear interactions between electrical and hemodynamic signals. Here, we explore electro-vascular phase-amplitude coupling (PAC) between low-frequency hemodynamic and high-frequency electrical oscillations during an auditory task. We further apply a temporally embedded canonical correlation analysis (tCCA)-general linear model (GLM)-based correction approach to reduce the possible effect of systemic physiology on fNIRS recordings. Before correction, we observed significant PAC between fNIRS and broadband EEG in the frontal region (p ≪ 0.05), β (p ≪ 0.05) and γ (p = 0.010) in the left temporal/temporoparietal (left auditory; LA) region, and γ (p = 0.032) in the right temporal/temporoparietal (right auditory; RA) region across the entire dataset. Significant differences in PAC across conditions (task versus silence) were observed in LA (p = 0.023) and RA (p = 0.049) γ sub-bands and in lower frequency (5-20 Hz) frontal activity (p = 0.005). After correction, significant fNIRS-γ-band PAC was observed in the frontal (p = 0.021) and LA (p = 0.025) regions, while fNIRS-α (p = 0.003) and fNIRS-β (p = 0.041) PAC were observed in RA. Decreased frontal γ-band (p = 0.008) and increased β-band (p ≪ 0.05) PAC were observed during the task. These outcomes represent the first characterization of electro-vascular PAC between fNIRS and EEG signals during an auditory task, providing insights into electro-vascular coupling in auditory processing.more » « less
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1002/hbm.26149
