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Bidirectional Neuronal Control of Epileptiform Activity by Repetitive Transcranial Focused Ultrasound Stimulations.

Authors: Choi T, Koo M, Joo J, Kim T, Shon YM, Park J

Repetitive stimulation procedures are used in neuromodulation techniques to induce persistent excitatory or inhibitory brain activity. The directivity of modulation is empirically regulated by modifying the stimulation length, interval, and strength. However, bidirectional neuronal modulations using ultrasound stimulations are rarely reported. This study presents bidirectional control of epileptiform activities with repetitive transcranial-focused ultrasound stimulations in a rat model of drug-induced acute epilepsy. It is found that repeated transmission of elongated (40 s), ultra-low pressure (0.25 MPa) ultrasound can fully suppress epileptic activities in electro-encephalography and cerebral blood volume measurements, while the change in bursting intervals from 40 to 20 s worsens epileptic activities even with the same burst length. Furthermore, the suppression induced by 40 s long bursts is transformed to excitatory states by a subsequent transmission. Bidirectional modulation of epileptic seizures with repeated ultrasound stimulation is achieved by regulating the changes in glutamate and γ-Aminobutyric acid levels, as confirmed by measurements of expressed c-Fos and GAD65 and multitemporal analysis of neurotransmitters in the interstitial fluid obtained via microdialysis.

Introduction

Purpose Transcranial ultrasound stimulation
Study Objective To determine whether repetitive transcranial-focused ultrasound can bidirectionally modulate epileptiform activity in a PTZ-induced rat model by varying stimulation parameters and to assess related changes in GABA and glutamate.
Animal model / Human subject rat, none, none, none
Disease model epilepsy (drug-induced acute epilepsy in a rat model)

Outcomes and Safety

Summary of Outcomes Repetitive transcranial focused ultrasound produced bidirectional control of PTZ‑induced seizures in rats: sustained anticonvulsant effects (reduced EEG spike counts and CBV, increased extracellular GABA and GAD65, decreased c‑Fos) were achieved with low‑pressure elongated bursts (TXL_40_40: 0.25 MPa, 40 s bursts, 40 s interval, 6 repeats), whereas shorter inter‑burst intervals (TXL_40_20: 0.25 MPa, 40 s bursts, 20 s interval), short high‑pressure bursts (TXH_0.25_30: 1 MPa, 0.25 s bursts, 30 s interval), and a hybrid sequence (TX_HYBRID: TXL_40_40 followed by TXH_0.25_30) produced rebound or excitatory effects.
Duration of biological effect 30 min
Safety-related matter Certain stimulation patterns induced hippocampal damage, while others showed no tissue damage.

Brain Region

Visualization unavailable

Ultrasound Parameters

Ultrasound instrument not reported
FUS Frequency not reported
FUS Intensity not reported
FUS Pressure 0.25 MPa
FUS Mode pulsed
Pulse duration 40 s
Duration of a single FUS session 40 s
Treatment frequency Multiple sessions

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