Deep brain stimulation (DBS) is a promising neuromodulation therapy, but the neurophysiological mechanisms of DBS remain unclear. In awake mice, we performed high-speed membrane voltage fluorescence imaging of individual hippocampal CA1 neurons during DBS delivered at 40 Hz or 140 Hz, free of electrical interference. DBS powerfully depolarized somatic membrane potentials without suppressing spike rate, especially at 140 Hz. Further, DBS paced membrane voltage and spike timing at the stimulation frequency and reduced timed spiking output in response to hippocampal network theta-rhythmic (3–12 Hz) activity patterns. To determine whether DBS directly impacts cellular processing of inputs, we optogenetically evoked theta-rhythmic membrane depolarization at the soma. We found that DBS-evoked membrane depolarization was correlated with DBS-mediated suppression of neuronal responses to optogenetic inputs. These results demonstrate that DBS produces powerful membrane depolarization that interferes with the ability of individual neurons to respond to inputs, creating an informational lesion.
Deep brain stimulation creates informational lesion through membrane depolarization in mouse hippocampus
E. Lowet,Krishnakanth Kondabolu,Samuel Zhou,Rebecca A. Mount,Yangyang Wang,Cara Ravasio,Xue Han
Published 2022 in Nature Communications
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- Publication year
2022
- Venue
Nature Communications
- Publication date
2022-12-13
- Fields of study
Medicine
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Semantic Scholar, PubMed
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