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Effects of transcranial focused ultrasound stimulation to human lateral geniculate nucleus on visual perception and steady-state visual evoked potentials

Martin TW Scott, Patti N Limon, Morteza Mohammadjavadi, Benjamin R. Kop, Nai-Feng Chen, Eva A Feredoes, Vladimir Vildavski, Gerald R Popelka, Anthony M. Norcia, Kim Butts Pauly, Ryan T Ash

2026 · 10.64898/2026.07.30.741804

human healthyhealthyeeg megbehaviour

Abstract

Transcranial ultrasound stimulation (TUS) is an emerging tool to non-invasively modulate neural activity in deep brain areas. A key need in accelerating TUS into cognitive neuroscience and neuropsychiatry is to better understand how different sonication parameters relate to neuromodulatory effects. Here we assess the role of pulse repetition frequency (PRF), a key TUS parameter thought to determine the relative contribution of molecular displacement and acoustic radiation force effects on neural tissue using the human subcortical visual pathway as a testbed. We combined frequency-tagged steady-state visual evoked potential (SSVEP) measures of contrast-response with contrast increment detection psychophysics as neural and behavioral readouts of visual pathway function. We used structural MRIs and acoustic simulations to target the lateral geniculate nucleus (LGN). Concurrent with visual stimulus presentation, the left LGN or a more superficial control site were stimulated with a neuronavigated depth-steerable 4-element TUS transducer at a range of PRFs with 68 W/cm 2 free-water I SPPA , and a 10% duty cycle. An effective white-noise auditory mask blinded participants to stimulation conditions. Recordings from 25 neurotypical participants failed to detect any impact of TUS on SSVEP response amplitude, SSVEP response latency, or perceptual behavior. Analysis of simulations generated from the measured transducer positions grant reasonably high confidence that the LGN was within the TUS focus in most participants, with no correlation between targeting accuracy and changes in activity during TUS. Our results provide a cautionary note about the effect size of neuronavigated TUS for online causal manipulations in cognitive and clinical neuroscience.

Abstract via europepmc.

Specieshuman
Subjects25 participants
Sessions per subject1
Randomisedyes
Blindingdouble
Sham / controlactive control site
Auditory controlmasking sound, ramped pulses
Readout timingboth
Anaesthesianot applicable
Readoutseeg meg, behaviour — steady-state visual evoked potential amplitude and phase; contrast increment detection psychophysics
Direction of effectno effectNo effect of LGN or control-site TUS at any PRF on SSVEP amplitude, latency or contrast-increment detection, online or offline.
Adverse eventsnone observedNo apparent visual percepts or discomfort at the TUS site were reported; BabelBrain thermal simulation gave a maximum temperature rise of 0.5 C at the target.

Exposures

Exposure 1: LGN-TUS (70 mm depth)

Target: lateral geniculate nucleus — “left LGN”
Device: NeuroFUS · Sonic Concepts (sold by Brainbox) · NeuroFUS Pro CTX-500, 4-element annular transducer ✓

Pulse timing
Waveformpulsed
Fundamental frequency (kHz)500✓✓✓
Pulse duration (ms)not reported⚑
Pulse repetition frequency (Hz)4.88, 48.75, 487.5swept✓✓✓
Duty cycle (%)10✓✓✓
Sonication duration (s)12✓✓✓⚑
Pressure and intensity, by domain
Free-field pressure (kPa)1,400✓✓✓
Free-field Isppa (W/cm²)68✓✓✓
Free-field Ispta (W/cm²)not reported
In-situ estimatesimulationmean or range across subjects
In-situ pressure (kPa)690✓✓✓⚑
In-situ Isppa (W/cm²)16.2✓✓✓⚑
In-situ Ispta (W/cm²)not reported
Protocol, in the paper’s words

12 s trains at 10% duty cycle, PRF randomised trial by trial among 4.875, 48.75 and 487.5 Hz, with 5% linear ramps on the pulses at the two lower PRFs; synchronised with visual stimulus onset; eight 16-trial TUS blocks interleaved with no-TUS trials, depth 70 mm (LGN) or 30 mm (control).

Exposure 2: Control-TUS (30 mm depth)

Target: white matter, auditory cortex — “a more superficial control site in the auditory cortex and subcortical white matter”
Device: NeuroFUS · Sonic Concepts (sold by Brainbox) · NeuroFUS Pro CTX-500, 4-element annular transducer ✓

Pulse timing
Waveformpulsed
Fundamental frequency (kHz)500✓✓✓
Pulse duration (ms)not reported
Pulse repetition frequency (Hz)4.88, 48.75, 487.5swept✓✓✓
Duty cycle (%)10✓✓✓
Sonication duration (s)12✓✓✓
Pressure and intensity, by domain
Free-field pressure (kPa)1,400✓✓✓
Free-field Isppa (W/cm²)68✓✓✓
Free-field Ispta (W/cm²)not reported
In-situ estimatenot reported
In-situ pressure (kPa)not reported
In-situ Isppa (W/cm²)not reported
In-situ Ispta (W/cm²)not reported
Protocol, in the paper’s words

12 s trains at 10% duty cycle, PRF randomised trial by trial among 4.875, 48.75 and 487.5 Hz, with 5% linear ramps on the pulses at the two lower PRFs; synchronised with visual stimulus onset; eight 16-trial TUS blocks interleaved with no-TUS trials, depth 70 mm (LGN) or 30 mm (control).

Flags from extraction

  • n_subjects — Text says n=25 and 'Twenty-five subjects were retained with 2 rejected', implying 27 enrolled; 25 recorded.
  • exposures[0].timing.sonication_duration_s — Trains stated as 12 s, but trial text also says 11 s trials and 10.667 s of TUS per 13.333 s trial.
  • exposures[0].in_situ.isppa_w_cm2 — Results give mean simulated in situ Isppa 16.2 W/cm2 (range 8.5-20.5) while the Discussion says about 8 W/cm2 on average at the target.
  • exposures[0].in_situ.pressure_kpa — 0.69 +/- 0.33 MPa is a peak negative pressure, with range 0.5-0.78; the SD looks inconsistent with the range.
  • exposures[1].target.terms — Control site is described as auditory cortex and subcortical white matter at 30 mm depth; no separate dosimetry reported.
  • exposures[0].timing.pulse_duration_ms — Pulse duration not stated; duty cycle and PRF are given but no arithmetic done.
  • sham_type — Mask-only no-TUS trials were also interleaved; whether the transducer was powered off is not stated.