← Explore

Effects of online motor cortex transcranial ultrasound stimulation on interhemispheric inhibition

Yanqiu Wang, Ke Zeng, Anton Fomenko, Xue Xia, Mandy Yi Rong Ding, Jean‐François Nankoo, Robert Chen

The Journal of Physiology 2026 · 10.1113/jp290803

human healthyhealthyemg mep

Abstract

Transcranial ultrasound stimulation (TUS) of the motor cortex (M1) has been found to modulate interhemispheric inhibition (IHI) after sonication (offline effect). However, the effects of M1 TUS on IHI during sonication (online effect) remain unknown. The current study examined the effects of online M1 TUS on IHI from the sonicated M1 to the contralateral M1 and on the contralateral M1 excitability in 15 healthy subjects. IHI was measured with paired-pulse transcranial magnetic stimulation (TMS) at 10 ms (short-latency IHI, SIHI) or 40 ms (long-latency IHI, LIHI) interstimulus interval (ISI), and the contralateral M1 excitability was measured with single-pulse TMS. The results showed that online TUS decreased the sonicated M1 to the contralateral M1 at LIHI but not at SIHI, while the contralateral TUS M1 excitability was unchanged. TUS may modulate complex circuits that mediate LIHI. These findings showed that TUS can be used to investigate the functional interactions between the two hemispheres. KEY POINTS: Offline non-invasive brain stimulations have been shown to modulate interhemispheric inhibition. The current study examined the effects of online primary motor cortex (M1) transcranial ultrasound stimulation (TUS) on interhemispheric inhibition from the sonicated M1 to the contralateral M1, and the contralateral M1 excitability. TUS decreased long- but not short-latency interhemispheric inhibition from the sonicated M1 to the contralateral M1. TUS could be a tool for investigating functional interactions between the two hemispheres.

Abstract via europepmc.

Specieshuman
Subjects15 participants
Sessions per subject1
Randomisedyes
Blindingnot reported
Sham / controlinactive transducer
Auditory controlmasking sound
Readout timingonline
Anaesthesianot applicable
Readoutsemg mep — paired-pulse TMS interhemispheric inhibition (SIHI 10 ms, LIHI 40 ms ISI); MEP amplitude in FDI
Direction of effectmixed or unclearOnline right M1 TUS reduced long-latency IHI (higher LIHI ratio) versus sham but not short-latency IHI, and left M1 excitability was unchanged; sonicated M1 MEPs were reduced versus baseline but not significantly versus sham.
Adverse eventsnot reported

Exposures

Exposure 1: Online right M1 TUS (500 ms, with TMS conditioning pulse at 490 ms)

Target: primary motor cortex — “right M1”
Device: Sonic Concepts · Sonic Concepts Inc. · custom two-element annular array H246; TPO201-80 driver ✓

Pulse timing
Waveformpulsed
Fundamental frequency (kHz)500✓✓✓
Pulse duration (ms)not reportedimplied by duty cycle ÷ PRF: 0.1 ms (not stated by the paper)⚑
Pulse repetition frequency (Hz)1,000✓✓✓
Duty cycle (%)10✓✓✓
Sonication duration (s)0.5✓✓✓
Pressure and intensity, by domain
Free-field pressure (kPa)not reported
Free-field Isppa (W/cm²)11.73✓✓✓
Free-field Ispta (W/cm²)1.17✓✓✓
In-situ estimatederatingsingle value
In-situ pressure (kPa)not reported
In-situ Isppa (W/cm²)2.93✓✓✓⚑
In-situ Ispta (W/cm²)0.29✓✓✓
Protocol, in the paper’s words

Sonication depth 30 mm, 20 W, 1000 Hz PRF, 10% duty cycle and 500 ms duration; a TMS conditioning pulse was delivered 10 ms before the end of sonication (SIHI) or TS at end or 30 ms after; 5 s intertrial interval.

Flags from extraction

  • exposures[0].in_situ.isppa_w_cm2 — In situ values are estimated by assuming 75% skull attenuation (derating), not measured through skull.
  • n_subjects — 18 recruited, 3 withdrawn for high TMS motor threshold; 15 analysed and recorded.
  • n_sessions_per_subject — Experiments 1-3 are described within a 2.5-3 h visit; number of sessions across experiments not clearly stated.
  • exposures[0].timing.pulse_duration_ms — Pulse duration not stated (duty cycle and PRF given only).