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Induced neural phase precession through exogeneous electric fields

The gradual shifting of preferred neural spiking relative to local field potentials (LFPs), known as phase precession, plays a prominent role in neural coding. Correlations between the phase precession and behavior have been observed throughout various brain regions. As such, phase precession is sug...

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Autores principales: Wischnewski, M., Tran, H., Zhao, Z., Shirinpour, S., Haigh, Z.J., Rotteveel, J., Perera, N.D., Alekseichuk, I., Zimmermann, J., Opitz, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081336/
https://www.ncbi.nlm.nih.gov/pubmed/37034780
http://dx.doi.org/10.1101/2023.03.31.535073
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author Wischnewski, M.
Tran, H.
Zhao, Z.
Shirinpour, S.
Haigh, Z.J.
Rotteveel, J.
Perera, N.D.
Alekseichuk, I.
Zimmermann, J.
Opitz, A.
author_facet Wischnewski, M.
Tran, H.
Zhao, Z.
Shirinpour, S.
Haigh, Z.J.
Rotteveel, J.
Perera, N.D.
Alekseichuk, I.
Zimmermann, J.
Opitz, A.
author_sort Wischnewski, M.
collection PubMed
description The gradual shifting of preferred neural spiking relative to local field potentials (LFPs), known as phase precession, plays a prominent role in neural coding. Correlations between the phase precession and behavior have been observed throughout various brain regions. As such, phase precession is suggested to be a global neural mechanism that promotes local neuroplasticity. However, causal evidence and neuroplastic mechanisms of phase precession are lacking so far. Here we show a causal link between LFP dynamics and phase precession. In three experiments, we modulated LFPs in humans, a non-human primate, and computational models using alternating current stimulation. We show that continuous stimulation of motor cortex oscillations in humans lead to a gradual phase shift of maximal corticospinal excitability by ~90°. Further, exogenous alternating current stimulation induced phase precession in a subset of entrained neurons (~30%) in the non-human primate. Multiscale modeling of realistic neural circuits suggests that alternating current stimulation-induced phase precession is driven by NMDA-mediated synaptic plasticity. Altogether, the three experiments provide mechanistic and causal evidence for phase precession as a global neocortical process. Alternating current-induced phase precession and consequently synaptic plasticity is crucial for the development of novel therapeutic neuromodulation methods.
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spelling pubmed-100813362023-04-08 Induced neural phase precession through exogeneous electric fields Wischnewski, M. Tran, H. Zhao, Z. Shirinpour, S. Haigh, Z.J. Rotteveel, J. Perera, N.D. Alekseichuk, I. Zimmermann, J. Opitz, A. bioRxiv Article The gradual shifting of preferred neural spiking relative to local field potentials (LFPs), known as phase precession, plays a prominent role in neural coding. Correlations between the phase precession and behavior have been observed throughout various brain regions. As such, phase precession is suggested to be a global neural mechanism that promotes local neuroplasticity. However, causal evidence and neuroplastic mechanisms of phase precession are lacking so far. Here we show a causal link between LFP dynamics and phase precession. In three experiments, we modulated LFPs in humans, a non-human primate, and computational models using alternating current stimulation. We show that continuous stimulation of motor cortex oscillations in humans lead to a gradual phase shift of maximal corticospinal excitability by ~90°. Further, exogenous alternating current stimulation induced phase precession in a subset of entrained neurons (~30%) in the non-human primate. Multiscale modeling of realistic neural circuits suggests that alternating current stimulation-induced phase precession is driven by NMDA-mediated synaptic plasticity. Altogether, the three experiments provide mechanistic and causal evidence for phase precession as a global neocortical process. Alternating current-induced phase precession and consequently synaptic plasticity is crucial for the development of novel therapeutic neuromodulation methods. Cold Spring Harbor Laboratory 2023-10-30 /pmc/articles/PMC10081336/ /pubmed/37034780 http://dx.doi.org/10.1101/2023.03.31.535073 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Wischnewski, M.
Tran, H.
Zhao, Z.
Shirinpour, S.
Haigh, Z.J.
Rotteveel, J.
Perera, N.D.
Alekseichuk, I.
Zimmermann, J.
Opitz, A.
Induced neural phase precession through exogeneous electric fields
title Induced neural phase precession through exogeneous electric fields
title_full Induced neural phase precession through exogeneous electric fields
title_fullStr Induced neural phase precession through exogeneous electric fields
title_full_unstemmed Induced neural phase precession through exogeneous electric fields
title_short Induced neural phase precession through exogeneous electric fields
title_sort induced neural phase precession through exogeneous electric fields
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081336/
https://www.ncbi.nlm.nih.gov/pubmed/37034780
http://dx.doi.org/10.1101/2023.03.31.535073
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