A tool for monitoring cell type–specific focused ultrasound neuromodulation and control of chronic epilepsy

Author:

Murphy Keith R.1,Farrell Jordan S.2,Gomez Juan L.34,Stedman Quintin G.5,Li Ningrui6,Leung Steven A.6,Good Cameron H.7,Qiu Zhihai6,Firouzi Kamyar5,Butts Pauly Kim6,Khuri-Yakub Butrus Pierre T.5,Michaelides Michael34,Soltesz Ivan2,de Lecea Luis1

Affiliation:

1. Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305

2. Department of Neurosurgery, Stanford University, Stanford, CA 94305

3. Biobehavioral Imaging and Molecular Neuropsychopharmacology Unit, National Institute on Drug Abuse, Baltimore, MD 21224

4. Department of Radiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205

5. Department of Electrical Engineering, Stanford University, Stanford, CA 94305

6. Department of Radiology, Stanford University, Stanford, CA 94305

7. Querrey Simpson Institute for Bioelectronics, Northwestern University, Evanston, IL 60601

Abstract

Focused ultrasound (FUS) is a powerful tool for noninvasive modulation of deep brain activity with promising therapeutic potential for refractory epilepsy; however, tools for examining FUS effects on specific cell types within the deep brain do not yet exist. Consequently, how cell types within heterogeneous networks can be modulated and whether parameters can be identified to bias these networks in the context of complex behaviors remains unknown. To address this, we developed a fiber Photometry Coupled focused Ultrasound System (PhoCUS) for simultaneously monitoring FUS effects on neural activity of subcortical genetically targeted cell types in freely behaving animals. We identified a parameter set that selectively increases activity of parvalbumin interneurons while suppressing excitatory neurons in the hippocampus. A net inhibitory effect localized to the hippocampus was further confirmed through whole brain metabolic imaging. Finally, these inhibitory selective parameters achieved significant spike suppression in the kainate model of chronic temporal lobe epilepsy, opening the door for future noninvasive therapies.

Funder

HHS | NIH | National Institute of Mental Health

HHS | NIH | National Institute on Drug Abuse

HHS | NIH | National Heart, Lung, and Blood Institute

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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