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Voluntary control of intracortical oscillations for reconfiguration of network activity

Voluntary control of oscillatory activity represents a key target in the self-regulation of brain function. Using a real-time closed-loop paradigm and simultaneous macro- and micro-electrode recordings, we studied the effects of self-induced intracortical oscillatory activity (4–8 Hz) in seven neuro...

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Autores principales: Corlier, Juliana, Valderrama, Mario, Navarrete, Miguel, Lehongre, Katia, Hasboun, Dominique, Adam, Claude, Belaid, Hayat, Clémenceau, Stéphane, Baulac, Michel, Charpier, Stéphane, Navarro, Vincent, Le Van Quyen, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093688/
https://www.ncbi.nlm.nih.gov/pubmed/27808225
http://dx.doi.org/10.1038/srep36255
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author Corlier, Juliana
Valderrama, Mario
Navarrete, Miguel
Lehongre, Katia
Hasboun, Dominique
Adam, Claude
Belaid, Hayat
Clémenceau, Stéphane
Baulac, Michel
Charpier, Stéphane
Navarro, Vincent
Le Van Quyen, Michel
author_facet Corlier, Juliana
Valderrama, Mario
Navarrete, Miguel
Lehongre, Katia
Hasboun, Dominique
Adam, Claude
Belaid, Hayat
Clémenceau, Stéphane
Baulac, Michel
Charpier, Stéphane
Navarro, Vincent
Le Van Quyen, Michel
author_sort Corlier, Juliana
collection PubMed
description Voluntary control of oscillatory activity represents a key target in the self-regulation of brain function. Using a real-time closed-loop paradigm and simultaneous macro- and micro-electrode recordings, we studied the effects of self-induced intracortical oscillatory activity (4–8 Hz) in seven neurosurgical patients. Subjects learned to robustly and specifically induce oscillations in the target frequency, confirmed by increased oscillatory event density. We have found that the session-to-session variability in performance was explained by the functional long-range decoupling of the target area suggesting a training-induced network reorganization. Downstream effects on more local activities included progressive cross-frequency-coupling with gamma oscillations (30–120 Hz), and the dynamic modulation of neuronal firing rates and spike timing, indicating an improved temporal coordination of local circuits. These findings suggest that effects of voluntary control of intracortical oscillations can be exploited to specifically target plasticity processes to reconfigure network activity, with a particular relevance for memory function or skill acquisition.
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spelling pubmed-50936882016-11-10 Voluntary control of intracortical oscillations for reconfiguration of network activity Corlier, Juliana Valderrama, Mario Navarrete, Miguel Lehongre, Katia Hasboun, Dominique Adam, Claude Belaid, Hayat Clémenceau, Stéphane Baulac, Michel Charpier, Stéphane Navarro, Vincent Le Van Quyen, Michel Sci Rep Article Voluntary control of oscillatory activity represents a key target in the self-regulation of brain function. Using a real-time closed-loop paradigm and simultaneous macro- and micro-electrode recordings, we studied the effects of self-induced intracortical oscillatory activity (4–8 Hz) in seven neurosurgical patients. Subjects learned to robustly and specifically induce oscillations in the target frequency, confirmed by increased oscillatory event density. We have found that the session-to-session variability in performance was explained by the functional long-range decoupling of the target area suggesting a training-induced network reorganization. Downstream effects on more local activities included progressive cross-frequency-coupling with gamma oscillations (30–120 Hz), and the dynamic modulation of neuronal firing rates and spike timing, indicating an improved temporal coordination of local circuits. These findings suggest that effects of voluntary control of intracortical oscillations can be exploited to specifically target plasticity processes to reconfigure network activity, with a particular relevance for memory function or skill acquisition. Nature Publishing Group 2016-11-03 /pmc/articles/PMC5093688/ /pubmed/27808225 http://dx.doi.org/10.1038/srep36255 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Corlier, Juliana
Valderrama, Mario
Navarrete, Miguel
Lehongre, Katia
Hasboun, Dominique
Adam, Claude
Belaid, Hayat
Clémenceau, Stéphane
Baulac, Michel
Charpier, Stéphane
Navarro, Vincent
Le Van Quyen, Michel
Voluntary control of intracortical oscillations for reconfiguration of network activity
title Voluntary control of intracortical oscillations for reconfiguration of network activity
title_full Voluntary control of intracortical oscillations for reconfiguration of network activity
title_fullStr Voluntary control of intracortical oscillations for reconfiguration of network activity
title_full_unstemmed Voluntary control of intracortical oscillations for reconfiguration of network activity
title_short Voluntary control of intracortical oscillations for reconfiguration of network activity
title_sort voluntary control of intracortical oscillations for reconfiguration of network activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093688/
https://www.ncbi.nlm.nih.gov/pubmed/27808225
http://dx.doi.org/10.1038/srep36255
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