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Frequency-Dependent Modulation of the Prefrontal Cortex by Low-Intensity Focused Ultrasound: Impact on Mesolimbic Dopamine Signaling

Greatness O. Olaitan, Akhabue K. Okojie, Wendy J. Lynch, B. Jill Venton

2025 · 10.1101/2025.10.26.684693

rodenthealthyotherhistology molecular

Abstract

Synchronized neural oscillations are fundamental for cognitive function and orchestrate inhibitory and excitatory neurotransmission and downstream signaling. We hypothesized that low-intensity focused ultrasound (LIFU) with frequency parameters mimicking oscillatory patterns would enable targeted neuromodulation. Building on prior findings of the ability of LIFU to modulate neurotransmission, we investigated the effects of frequency-modulated LIFU applied to the prelimbic cortex (PLC) on dopamine release in the nucleus accumbens (NAcc) core as well as neuronal and astrocytic activity. After three 80-second LIFU stimulations spaced 30 minutes apart, we found that LIFU excited or inhibited NAcc dopamine release for up to 90 minutes, and these effects were dependent on oscillation frequency and sex. In male rats, theta (8 Hz)-coupled beta (16 Hz) LIFU reduced both dopamine release by 58% and the level of the astrocytic marker GFAP by 50%. Similar decreases in dopamine density were observed in females. Delta (2 Hz)-coupled beta (16 Hz) stimulation produced similar inhibitory effects. Conversely, theta (5 Hz)-coupled gamma (50 Hz) LIFU increased dopamine release by 28% in males. However, similar excitation levels were observed only in females with an increased gamma frequency of 70 Hz (coupled with a theta frequency of 7 Hz). Histological analysis revealed no cell death, but both 8:16 Hz and 5:50 Hz LIFU elevated neuronal activation (cFOS) in the PLC in males, while 5:50 Hz also upregulated GFAP by 30%, suggesting astrocytic involvement. Thus, LIFU stimulation of the PLC can be frequency-tuned to selectively excite or inhibit dopaminergic signaling in the NAcc, suggesting a novel approach for manipulating neurotransmission.

Abstract via europepmc.

Speciesrat (Sprague-Dawley)
Subjects47 animals
Sessions per subject3
Randomisedyes
Blindingnot reported
Sham / controlinactive transducer, active control site
Auditory controlnot reported
Readout timingoffline
Anaesthesiaanaesthetised
Readoutsother, histology molecular — fast-scan cyclic voltammetry of electrically evoked dopamine in nucleus accumbens core; c-Fos, NeuN and GFAP immunofluorescence; H&E
Direction of effectbidirectional8:16 Hz and 2:16 Hz PRF patterns reduced evoked NAcc dopamine release (about 58 % for 8:16 Hz in males); 5:50 Hz increased it by about 28 % in males, and 7:70 Hz increased it in females.
Adverse eventsnone observedH&E staining revealed no overt cell death.

Exposures

Exposure 1: LIFU to prelimbic cortex, frequency-coupled PRF patterns

Target: ventromedial prefrontal cortex — “prelimbic cortex (PLC)”
Device: Olympus / Panametrics · Olympus-ims · XMS-310-B

Pulse timing
Waveformpulsed, continuous
Fundamental frequency (kHz)10,000✓✓✓
Pulse duration (ms)62.5, 35.7, 20, 14.29swept✓✓✓⚑
Pulse repetition frequency (Hz)8, 2, 7, 5, 50swept✓✓✓
Duty cycle (%)50, 12.5, 25, 10, 100swept✓✓✓⚑
Sonication duration (s)80✓✓✓
Pressure and intensity, by domain
Free-field pressure (kPa)not reported
Free-field Isppa (W/cm²)not reported
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

Three successive 80 s LIFU trains separated by 30 minutes between electrically evoked dopamine measurements; PRF/duty cycle pairs 8 Hz/50 %, 2 Hz/12.5 %, 7 Hz/25 %, 5 Hz/10 %, 7 Hz/10 % and 50 Hz/100 % (gamma only). Table gives a pulse interval (PI) per pattern, not labelled as pulse duration.

Flags from extraction

  • exposures[0].unspecified_domain — Only a 'spatial average intensity of 13 W/cm2' is given; not recorded because it is not stated as Isppa or Ispta and no pressure is given.
  • exposures[0].timing.pulse_duration_ms — Table 1 lists a pulse interval (PI) per pattern (e.g. 62.5 ms at 8 Hz, DC 50 %); not recorded as pulse duration.
  • exposures[0].timing.duty_cycle_pct — Duty cycle list holds the distinct table values: 50, 12.5, 25, 10 (two patterns) and 100 (50 Hz gamma only).
  • n_subjects — 47 rats stated; group n in figure legends is 5 or 6.
  • n_sessions_per_subject — Each animal received three trains in one experiment; session count not stated.