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Distinct Beta-band Oscillatory Circuits Underlie Corticospinal Gain Modulation
Rhythmic synchronization of neurons is known to affect neuronal interactions. In the motor system, oscillatory power fluctuations modulate corticospinal excitability. However, previous research addressing phase-specific gain modulation in the motor system has resulted in contradictory findings. It r...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093341/ https://www.ncbi.nlm.nih.gov/pubmed/29415124 http://dx.doi.org/10.1093/cercor/bhy016 |
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author | Khademi, Fatemeh Royter, Vladimir Gharabaghi, Alireza |
author_facet | Khademi, Fatemeh Royter, Vladimir Gharabaghi, Alireza |
author_sort | Khademi, Fatemeh |
collection | PubMed |
description | Rhythmic synchronization of neurons is known to affect neuronal interactions. In the motor system, oscillatory power fluctuations modulate corticospinal excitability. However, previous research addressing phase-specific gain modulation in the motor system has resulted in contradictory findings. It remains unclear how many time windows of increased responsiveness each oscillatory cycle provides. Moreover, we still lack conclusive evidence as to whether the motor cortex entails an intrinsic response modulation along the rhythm cycle, as shown for spinal neurons. We investigated this question with single-pulse transcranial magnetic stimulation over the primary motor cortex at rest. Application of near-motor threshold stimuli revealed a frequency- and phase-specific gain modulation at both cortical and spinal level, independent of the spontaneous oscillatory power fluctuations at each level. We detected bilateral sensorimotor circuits in the lower beta-band (14–17 Hz) and unilateral corticospinal circuits in the upper beta-band (20–24 Hz). These findings provide novel evidence that intrinsic activity in the human motor cortex modulates input gain along the beta oscillatory cycle within distinct circuits. In accordance with periodic alternations of synchronous hyper- and depolarization, increased neuronal responsiveness occurred once per oscillatory beta cycle. This information may lead to new brain state-dependent and circuit-specific interventions for targeted neuromodulation. |
format | Online Article Text |
id | pubmed-6093341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60933412018-08-22 Distinct Beta-band Oscillatory Circuits Underlie Corticospinal Gain Modulation Khademi, Fatemeh Royter, Vladimir Gharabaghi, Alireza Cereb Cortex Original Articles Rhythmic synchronization of neurons is known to affect neuronal interactions. In the motor system, oscillatory power fluctuations modulate corticospinal excitability. However, previous research addressing phase-specific gain modulation in the motor system has resulted in contradictory findings. It remains unclear how many time windows of increased responsiveness each oscillatory cycle provides. Moreover, we still lack conclusive evidence as to whether the motor cortex entails an intrinsic response modulation along the rhythm cycle, as shown for spinal neurons. We investigated this question with single-pulse transcranial magnetic stimulation over the primary motor cortex at rest. Application of near-motor threshold stimuli revealed a frequency- and phase-specific gain modulation at both cortical and spinal level, independent of the spontaneous oscillatory power fluctuations at each level. We detected bilateral sensorimotor circuits in the lower beta-band (14–17 Hz) and unilateral corticospinal circuits in the upper beta-band (20–24 Hz). These findings provide novel evidence that intrinsic activity in the human motor cortex modulates input gain along the beta oscillatory cycle within distinct circuits. In accordance with periodic alternations of synchronous hyper- and depolarization, increased neuronal responsiveness occurred once per oscillatory beta cycle. This information may lead to new brain state-dependent and circuit-specific interventions for targeted neuromodulation. Oxford University Press 2018-04 2018-02-03 /pmc/articles/PMC6093341/ /pubmed/29415124 http://dx.doi.org/10.1093/cercor/bhy016 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Khademi, Fatemeh Royter, Vladimir Gharabaghi, Alireza Distinct Beta-band Oscillatory Circuits Underlie Corticospinal Gain Modulation |
title | Distinct Beta-band Oscillatory Circuits Underlie Corticospinal Gain Modulation |
title_full | Distinct Beta-band Oscillatory Circuits Underlie Corticospinal Gain Modulation |
title_fullStr | Distinct Beta-band Oscillatory Circuits Underlie Corticospinal Gain Modulation |
title_full_unstemmed | Distinct Beta-band Oscillatory Circuits Underlie Corticospinal Gain Modulation |
title_short | Distinct Beta-band Oscillatory Circuits Underlie Corticospinal Gain Modulation |
title_sort | distinct beta-band oscillatory circuits underlie corticospinal gain modulation |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093341/ https://www.ncbi.nlm.nih.gov/pubmed/29415124 http://dx.doi.org/10.1093/cercor/bhy016 |
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