Transcallosal generation of phase-aligned beta bursts underlies TMS-induced interhemispheric inhibition

The excitability of the sensorimotor (SM1) cortices is reflected in the bilateral ~20 Hz beta oscillations. The extent to which these oscillations subtend the interhemispheric inhibition (IHI) captured by the Transcranial Magnetic Stimulation (TMS) ipsilateral Silent Period (iSP) protocol remains unclear. Therefore, we investigated the relationship between movement-related beta suppression and the iSP, along with their role for manual dexterity. Forty adults underwent an Electroencephalography assessment of beta suppression during volitional left-hand movement and a TMS assessment of iSP recorded from the right hand. In both cases, left SM1 beta oscillations (contralateral to the activated right SM1) were monitored through a proxy signal-the Electromyography of the contracted right hand. Bimanual dexterity was assessed with the Purdue Pegboard. Volitional movement caused significant bilateral SM1 beta suppression in nearly all participants (≥85%). ISPs were observed in every participant. In the proxy signal for the left SM1, the iSP coincided with TMS-evoked high-amplitude beta bursts. These bursts showed significant phase alignment across participants 10-70 ms after the TMS pulse. There was no significant association between the left-/right-hemisphere beta suppression, iSP, and bimanual dexterity. Our results highlight the distinct nature of beta oscillation changes during volitional movement compared with TMS-iSP and show that TMS induces IHI via transcallosal generation of phase-aligned beta bursts. Furthermore, our data suggest that only the initial phase of a beta burst carries an inhibitory effect. It also highlights the possibility of evoking a beta burst with the iSP protocol, opening perspectives for future neuroimaging and modeling studies.

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Publication Details

Journal
Imaging Neuroscience
Published
2025-01-01
DOI
https://doi.org/10.1162/imag_a_00570
Citations
3
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
2.73

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article

Transcallosal generation of phase-aligned beta bursts underlies TMS-induced interhemispheric inhibition

Pierre Cabaraux, Gilles Naeije, Mathieu Bourguignon, Julie Duqué et al.
3 citations
Imaging Neuroscience
Neuroscience and Neuropharmacology Research
2.73
article

Transcallosal generation of phase-aligned beta bursts underlies TMS-induced interhemispheric inhibition

Pierre Cabaraux, Gilles Naeije, Mathieu Bourguignon, Julie Duqué, Scott J. Mongold, Christian Georgiev
article en
3 citations

Abstract

The excitability of the sensorimotor (SM1) cortices is reflected in the bilateral ~20 Hz beta oscillations. The extent to which these oscillations subtend the interhemispheric inhibition (IHI) captured by the Transcranial Magnetic Stimulation (TMS) ipsilateral Silent Period (iSP) protocol remains unclear. Therefore, we investigated the relationship between movement-related beta suppression and the iSP, along with their role for manual dexterity. Forty adults underwent an Electroencephalography assessment of beta suppression during volitional left-hand movement and a TMS assessment of iSP recorded from the right hand. In both cases, left SM1 beta oscillations (contralateral to the activated right SM1) were monitored through a proxy signal-the Electromyography of the contracted right hand. Bimanual dexterity was assessed with the Purdue Pegboard. Volitional movement caused significant bilateral SM1 beta suppression in nearly all participants (≥85%). ISPs were observed in every participant. In the proxy signal for the left SM1, the iSP coincided with TMS-evoked high-amplitude beta bursts. These bursts showed significant phase alignment across participants 10-70 ms after the TMS pulse. There was no significant association between the left-/right-hemisphere beta suppression, iSP, and bimanual dexterity. Our results highlight the distinct nature of beta oscillation changes during volitional movement compared with TMS-iSP and show that TMS induces IHI via transcallosal generation of phase-aligned beta bursts. Furthermore, our data suggest that only the initial phase of a beta burst carries an inhibitory effect. It also highlights the possibility of evoking a beta burst with the iSP protocol, opening perspectives for future neuroimaging and modeling studies.

Imaging NeuroscienceVol. 3
Université Libre de Bruxelles (BE), Erasmus Hospital (BE), Walloon Excellence in Lifesciences and Biotechnology (BE), UCLouvain (BE)
Fonds De La Recherche Scientifique - FNRS
Openalex Percentile: Top 11%
Neuroscience and Neuropharmacology Research
2.73
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