# Somatosensory evoked potentials and high-frequency oscillations after transcranial static magnetic stimulation over the primary somatosensory cortex

**Authors:** Yuki Tanaka, Aoki Takahashi, Riku Ishizaka, Kodai Minami, Taisei Miyazaki, Kenta Oguma, Nodoka Shimizume, Isamu Ozaki, Tatsunori Watanabe

PMC · DOI: 10.1038/s41598-026-38767-2 · Scientific Reports · 2026-02-05

## TL;DR

This study investigates how a non-invasive brain stimulation technique affects sensory processing in the somatosensory cortex.

## Contribution

The study reveals that tSMS over the primary somatosensory cortex selectively reduces thalamocortical input without affecting GABAergic interneurons.

## Key findings

- tSMS over the primary somatosensory cortex significantly reduced early HFO amplitudes 20 minutes post-stimulation.
- Late HFOs and standard SEPs (N20 component) remained unaffected by tSMS.
- Early HFOs are linked to thalamocortical fibers, while late HFOs reflect GABAergic interneuron activity.

## Abstract

Transcranial static magnetic field stimulation (tSMS) is a non-invasive brain stimulation technique known to reduce cortical excitability. Although its effectiveness has been demonstrated in various cortical regions, it remains unclear whether somatosensory processing is influenced by this stimulation. The purpose of this study was to investigate whether tSMS over the primary somatosensory cortex (S1) modulates somatosensory evoked potentials (SEPs) and high-frequency oscillations superimposed on them (somatosensory HFOs). In a randomized crossover study, twenty healthy young adults received tSMS or sham stimulation over the left S1 (corresponding to C3 of the international 10–20 system) for 20 min. SEPs were recorded in response to right median nerve stimulation before, immediately after, and 20 min after stimulation. Somatosensory HFOs were extracted by applying a 400–800 Hz band-pass filter to SEP waveforms and separated into early and late components relative to the N20 peak latency. TSMS over the left S1 significantly reduced the amplitude of early HFOs 20 min after stimulation, whereas late HFOs remained unchanged. No effects of tSMS were observed on the N20 component of standard SEPs, which reflects neural activity in area 3b of the S1. Early and late HFOs are thought to reflect the action potentials of thalamocortical fibers and the activity of GABAergic interneurons, respectively. These findings therefore suggest that tSMS over the S1 selectively attenuates thalamocortical input while exerting no effect on GABAergic interneuron activity.

The online version contains supplementary material available at 10.1038/s41598-026-38767-2.

## Full-text entities

- **Diseases:** neurological, psychiatric, cognitive, orthopedic, or cardiopulmonary disorders (MESH:D009140), amyotrophic lateral sclerosis (MESH:D000690), stroke (MESH:D020521), muscle twitch (MESH:D019042), Parkinson's disease (MESH:D010300)
- **Chemicals:** calcium (MESH:D002118), NdFeB (-), sodium (MESH:D012964), neodymium (MESH:D009354), phospholipid (MESH:D010743), chloride (MESH:D002712)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12929797/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929797/full.md

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Source: https://tomesphere.com/paper/PMC12929797