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Transcranial ultrasonic stimulation modulates single-neuron discharge in macaques performing an antisaccade task
Nicolas Wattiez1, Charlotte Constans2, Thomas Deffieux2
1Institut du Cerveau et de la Moelle épinière, UMRS 975 INSERM, CNRS 7225, UMPC, Paris, France.
Brain Stimulation
|August 10, 2017
Summary
This study shows that low-intensity transcranial ultrasonic stimulation (TUS) can modulate neuronal activity in awake monkeys. Direct recordings reveal TUS effects, paving the way for refined neuromodulation techniques.
Area of Science:
- Neuroscience
- Neuromodulation
- Brain-computer interfaces
Background:
- Low-intensity transcranial ultrasonic stimulation (TUS) shows promise for non-invasive neuromodulation.
- Previous studies in rodents demonstrated robust effects, but human and large mammal studies yielded modest results.
- Direct recordings of neuronal responses to TUS are lacking, especially in primates.
Purpose of the Study:
- To investigate the effects of TUS on neuronal discharge in awake, behaving monkeys.
- To bridge the gap between rodent and human studies by using a primate model.
- To establish a method for real-time assessment of TUS effects on neuronal activity.
Main Methods:
- Simultaneous transcranial ultrasonic stimulation (TUS) of the frontal eye field (FEF) and recording of action potentials from the supplementary eye field (SEF) in macaques.
- Macaques performed an antisaccade task during stimulation.
- Control stimulation was applied to the visual cortex.
Main Results:
- SEF neuronal activity was significantly modulated shortly after TUS onset.
- 40% of recorded neurons showed significant changes in activity post-TUS.
- Half of the modulated neurons exhibited a transient increase in activity.
Conclusions:
- Non-invasive focused ultrasound's neuromodulatory effects can be assessed in real-time in awake primates.
- This method allows for direct measurement of TUS effects on single neurons.
- The findings support further parametric studies for optimizing TUS and facilitate the development of clinical TUS devices.

