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Unilateral online ultrasound stimulation of early visual cortex suppresses responses to contralateral visual stimuli

Suraya Dunsford, Keith Murphy, Ema Darrieutort, Elsa Fouragnan, Giorgio Ganis

Brain Stimulation 2026, 19, 103023 · 10.1016/j.brs.2025.103023

human healthyhealthyeeg megbehaviour

Abstract

Introduction Transcranial ultrasound stimulation (TUS) shows great promise for inducing neuroplastic changes that persist long after stimulation. Evidence of stimulation-locked (online) neural changes would enable the development of closed-loop application of TUS. However, such responses have been difficult to distinguish from coincident neural activity caused by auditory and somatosensory effects of TUS. Methods To dissociate genuine online neuromodulatory effects from peripheral confounds, we leveraged the contralateral retinotopic organization of the early visual cortex in nineteen subjects. Using a hemifield visual stimulation paradigm combined with high-precision, functional MRI-guided TUS, we applied TUS to the left early visual cortex while participants viewed checkerboards presented in the left or right visual hemifield. Randomized delivery of TUS on half of the trials enabled within-subject comparisons of hemisphere-specific, pattern-locked visual evoked potentials (VEPs) across stimulated and unstimulated hemispheres, as well as across visual-stimulus and no-stimulus conditions. Results TUS to the left visual cortex reduced mean VEP amplitude over the stimulated (left) hemisphere for right-hemifield (contralateral) stimuli. No such reduction appeared at the symmetric right-hemisphere sites for left-hemifield stimuli. The degree of online suppression correlated positively with target engagement, estimated by modelling the TUS field that accounted for inter-individual heterogeneity in skull transmission and its overlap with the fMRI-defined target. This relationship suggests that greater target engagement is reliably associated with stronger TUS-induced neural modulation. Conclusions These findings provide clear evidence of online, spatially specific TUS-induced neural modulation, dissociated from peripheral confounds. This approach establishes a robust framework for future studies aiming to map the TUS parameter space in real time by leveraging topographic organization to control for peripheral confounds, and supports the development of closed-loop neuromodulation protocols.

Abstract via europepmc.

Specieshuman
Subjects20 participants
Sessions per subject1
Randomisednot reported
Blindingnot reported
Sham / controlnone
Auditory controlmasking sound
Readout timingonline
Anaesthesianot applicable
Readoutseeg meg, behaviourVisual evoked potentials (VEPs) to hemifield checkerboard stimuli; behavioral hemifield discrimination accuracy
Direction of effectinhibitoryOnline TUS to the left early visual cortex reduced VEP amplitude at 60-100 ms and slowed P1 latency for contralateral (right hemifield) visual stimuli processed by the targeted hemisphere, with no such effect at the non-targeted right-hemisphere control site.
Adverse eventsnot reported

Exposures

Exposure 1: Online TUS to left early visual cortex during hemifield visual stimulation

Target: primary visual cortex — “left early visual cortex (calcarine sulcus)
Device: NeuroFUS · Sonic Concepts (sold by Brainbox) · NeuroFUS TPO system

Pulse timing
Waveformcontinuous
Fundamental frequency (kHz)500✓✓
Pulse duration (ms)not applicable
Pulse repetition frequency (Hz)not applicable
Duty cycle (%)100✓✓
Sonication duration (s)0.5✓✓
Pressure and intensity, by domain
Free-field pressure (kPa)not reported
Free-field Isppa (W/cm²)40✓✓
Free-field Ispta (W/cm²)not reported
In-situ estimatesimulationmean or range across subjects
In-situ pressure (kPa)310✓✓
In-situ Isppa (W/cm²)3.9✓✓
In-situ Ispta (W/cm²)not reported
Protocol, in the paper’s words

Each trial consisted of a single 500 ms continuous-wave pulse, time-locked to begin 400 ms before a 20-ms checkerboard visual stimulus. Each block comprised 100 trials (50 stimulation, 50 no-stimulation, alternating) with a 4.0 s inter-trial interval; 5 blocks were administered per session.

Flags from extraction

  • randomisedPaper does not state whether stimulation vs. no-stimulation trial order was formally randomized (described as alternating within blocks); left as not_reported.
  • blindingPaper does not describe participant or experimenter blinding to TUS vs. no-stimulation trials; not stated.
  • sham_typeStudy used a within-subject no-stimulation (NoS) control condition rather than a sham/placebo transducer condition; classified as sham_type none since there was no separate sham arm, only active-vs-no-stimulation trials.
  • exposures[0].in_situ.pressure_kpaTable 1 ROI-mask row reports mean pressure across participants at the functionally defined target (0.31±0.09 MPa); recorded as the mean per the mean±SD convention.