Individualized non-invasive deep brain stimulation of the basal ganglia using transcranial ultrasound stimulation

被引:0
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作者
Ghazaleh Darmani [1 ]
Hamidreza Ramezanpour [2 ]
Can Sarica [3 ]
Regina Annirood [1 ]
Talyta Grippe [2 ]
Jean-Francois Nankoo [1 ]
Anton Fomenko [1 ]
Brendan Santyr [1 ]
Ke Zeng [2 ]
Artur Vetkas [2 ]
Nardin Samuel [1 ]
Benjamin Davidson [4 ]
Alfonso Fasano [2 ]
Milad Lankarany [2 ]
Suneil K. Kalia [2 ]
Samuel Pichardo [1 ]
Andres M. Lozano [5 ]
Robert Chen [6 ]
机构
[1] University Health Network,Krembil Research Institute
[2] University of Toronto,Division of Neurosurgery, Department of Surgery
[3] York University,Department of Biology
[4] Beijing Normal University,Department of Psychology, Faculty of Arts and Sciences
[5] University of Toronto,Division of Neurology, Department of Medicine
[6] University Health Network,Edmond J. Safra Program in Parkinson’s Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital
[7] University of Calgary,Department of Radiology, Cumming School of Medicine
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D O I
10.1038/s41467-025-57883-7
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摘要
Transcranial ultrasound stimulation (TUS) offers precise, non-invasive neuromodulation, though its impact on human deep brain structures remains underexplored. Here we examined TUS-induced changes in the basal ganglia of 10 individuals with movement disorders (Parkinson’s disease and dystonia) and 15 healthy participants. Local field potentials were recorded using deep brain stimulation (DBS) leads in the globus pallidus internus (GPi). Compared to sham, theta burst TUS (tbTUS) increased theta power during stimulation, while 10 Hz TUS enhanced beta power, with effects lasting up to 40 min. In healthy participants, a stop-signal task assessed tbTUS effects on the GPi, with pulvinar stimulation serving as an active sham. GPi TUS prolonged stop-signal reaction times, indicating impaired response inhibition, whereas pulvinar TUS had no effect. These findings provide direct electrophysiological evidence of TUS target engagement and specificity in deep brain structures, suggesting its potential as a noninvasive DBS strategy for neurological and psychiatric disorders.
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