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Phase Dependency of the Human Primary Motor Cortex and Cholinergic Inhibition Cancelation During Beta tACS

The human motor cortex has a tendency to resonant activity at about 20 Hz so stimulation should more readily entrain neuronal populations at this frequency. We investigated whether and how different interneuronal circuits contribute to such resonance by using transcranial magnetic stimulation (TMS)...

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Detalles Bibliográficos
Autores principales: Guerra, Andrea, Pogosyan, Alek, Nowak, Magdalena, Tan, Huiling, Ferreri, Florinda, Di Lazzaro, Vincenzo, Brown, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028010/
https://www.ncbi.nlm.nih.gov/pubmed/27522077
http://dx.doi.org/10.1093/cercor/bhw245
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author Guerra, Andrea
Pogosyan, Alek
Nowak, Magdalena
Tan, Huiling
Ferreri, Florinda
Di Lazzaro, Vincenzo
Brown, Peter
author_facet Guerra, Andrea
Pogosyan, Alek
Nowak, Magdalena
Tan, Huiling
Ferreri, Florinda
Di Lazzaro, Vincenzo
Brown, Peter
author_sort Guerra, Andrea
collection PubMed
description The human motor cortex has a tendency to resonant activity at about 20 Hz so stimulation should more readily entrain neuronal populations at this frequency. We investigated whether and how different interneuronal circuits contribute to such resonance by using transcranial magnetic stimulation (TMS) during transcranial alternating current stimulation (tACS) at motor (20 Hz) and a nonmotor resonance frequency (7 Hz). We tested different TMS interneuronal protocols and triggered TMS pulses at different tACS phases. The effect of cholinergic short-latency afferent inhibition (SAI) was abolished by 20 Hz tACS, linking cortical beta activity to sensorimotor integration. However, this effect occurred regardless of the tACS phase. In contrast, 20 Hz tACS selectively modulated MEP size according to the phase of tACS during single pulse, GABAAergic short-interval intracortical inhibition (SICI) and glutamatergic intracortical facilitation (ICF). For SICI this phase effect was more marked during 20 Hz stimulation. Phase modulation of SICI also depended on whether or not spontaneous beta activity occurred at ~20 Hz, supporting an interaction effect between tACS and underlying circuit resonances. The present study provides in vivo evidence linking cortical beta activity to sensorimotor integration, and for beta oscillations in motor cortex being promoted by resonance in GABAAergic interneuronal circuits.
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spelling pubmed-50280102016-09-21 Phase Dependency of the Human Primary Motor Cortex and Cholinergic Inhibition Cancelation During Beta tACS Guerra, Andrea Pogosyan, Alek Nowak, Magdalena Tan, Huiling Ferreri, Florinda Di Lazzaro, Vincenzo Brown, Peter Cereb Cortex Original Articles The human motor cortex has a tendency to resonant activity at about 20 Hz so stimulation should more readily entrain neuronal populations at this frequency. We investigated whether and how different interneuronal circuits contribute to such resonance by using transcranial magnetic stimulation (TMS) during transcranial alternating current stimulation (tACS) at motor (20 Hz) and a nonmotor resonance frequency (7 Hz). We tested different TMS interneuronal protocols and triggered TMS pulses at different tACS phases. The effect of cholinergic short-latency afferent inhibition (SAI) was abolished by 20 Hz tACS, linking cortical beta activity to sensorimotor integration. However, this effect occurred regardless of the tACS phase. In contrast, 20 Hz tACS selectively modulated MEP size according to the phase of tACS during single pulse, GABAAergic short-interval intracortical inhibition (SICI) and glutamatergic intracortical facilitation (ICF). For SICI this phase effect was more marked during 20 Hz stimulation. Phase modulation of SICI also depended on whether or not spontaneous beta activity occurred at ~20 Hz, supporting an interaction effect between tACS and underlying circuit resonances. The present study provides in vivo evidence linking cortical beta activity to sensorimotor integration, and for beta oscillations in motor cortex being promoted by resonance in GABAAergic interneuronal circuits. Oxford University Press 2016-10 2016-09-19 /pmc/articles/PMC5028010/ /pubmed/27522077 http://dx.doi.org/10.1093/cercor/bhw245 Text en © The Author 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Guerra, Andrea
Pogosyan, Alek
Nowak, Magdalena
Tan, Huiling
Ferreri, Florinda
Di Lazzaro, Vincenzo
Brown, Peter
Phase Dependency of the Human Primary Motor Cortex and Cholinergic Inhibition Cancelation During Beta tACS
title Phase Dependency of the Human Primary Motor Cortex and Cholinergic Inhibition Cancelation During Beta tACS
title_full Phase Dependency of the Human Primary Motor Cortex and Cholinergic Inhibition Cancelation During Beta tACS
title_fullStr Phase Dependency of the Human Primary Motor Cortex and Cholinergic Inhibition Cancelation During Beta tACS
title_full_unstemmed Phase Dependency of the Human Primary Motor Cortex and Cholinergic Inhibition Cancelation During Beta tACS
title_short Phase Dependency of the Human Primary Motor Cortex and Cholinergic Inhibition Cancelation During Beta tACS
title_sort phase dependency of the human primary motor cortex and cholinergic inhibition cancelation during beta tacs
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028010/
https://www.ncbi.nlm.nih.gov/pubmed/27522077
http://dx.doi.org/10.1093/cercor/bhw245
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