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Induction of cortical plasticity for reciprocal muscles by paired associative stimulation

BACKGROUND: Paired associative stimulation (PAS) is widely used to induce plasticity in the human motor cortex. Although reciprocal inhibition of antagonist muscles plays a fundamental role in human movements, change in cortical circuits for reciprocal muscles by PAS is unknown. METHODS: We investig...

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Autores principales: Suzuki, Makoto, Kirimoto, Hikari, Sugawara, Kazuhiro, Watanabe, Makoto, Shimizu, Shinobu, Ishizaka, Ikuyo, Yamada, Sumio, Matsunaga, Atsuhiko, Fukuda, Michinari, Onishi, Hideaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212109/
https://www.ncbi.nlm.nih.gov/pubmed/25365805
http://dx.doi.org/10.1002/brb3.280
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author Suzuki, Makoto
Kirimoto, Hikari
Sugawara, Kazuhiro
Watanabe, Makoto
Shimizu, Shinobu
Ishizaka, Ikuyo
Yamada, Sumio
Matsunaga, Atsuhiko
Fukuda, Michinari
Onishi, Hideaki
author_facet Suzuki, Makoto
Kirimoto, Hikari
Sugawara, Kazuhiro
Watanabe, Makoto
Shimizu, Shinobu
Ishizaka, Ikuyo
Yamada, Sumio
Matsunaga, Atsuhiko
Fukuda, Michinari
Onishi, Hideaki
author_sort Suzuki, Makoto
collection PubMed
description BACKGROUND: Paired associative stimulation (PAS) is widely used to induce plasticity in the human motor cortex. Although reciprocal inhibition of antagonist muscles plays a fundamental role in human movements, change in cortical circuits for reciprocal muscles by PAS is unknown. METHODS: We investigated change in cortical plasticity for reciprocal muscles during PAS. PAS consisted of 200 pairs of peripheral electric stimulation of the right median nerve at the wrist at a frequency of 0.25 Hz followed by transcranial magnetic stimulation of the left M1 at the midpoint between the center of gravities of the flexor carpi radialis (FCR) and extensor carpi radialis (ECR) muscles. Measures of motor cortical excitability included resting motor threshold (RMT), GABA(A)-mediated short-interval intracortical inhibition (SICI), and GABA(B)-mediated long-interval intracortical inhibition (LICI). RESULTS: Motor evoked potential amplitude-conditioned LICI for the FCR muscle was significantly decreased after PAS (P = 0.020), whereas that for the ECR muscle was significantly increased (P = 0.033). Changes in RMT and SICI for the FCR and ECR muscles were not significantly different before and after PAS. Corticospinal excitability for both reciprocal muscles was increased during PAS, but GABA(B)-mediated cortical inhibitory functions for the agonist and antagonist muscles were reciprocally altered after PAS. CONCLUSION: These results implied that the cortical excitability for reciprocal muscles including GABA(B)-ergic inhibitory systems within human M1 could be differently altered by PAS.
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spelling pubmed-42121092014-10-30 Induction of cortical plasticity for reciprocal muscles by paired associative stimulation Suzuki, Makoto Kirimoto, Hikari Sugawara, Kazuhiro Watanabe, Makoto Shimizu, Shinobu Ishizaka, Ikuyo Yamada, Sumio Matsunaga, Atsuhiko Fukuda, Michinari Onishi, Hideaki Brain Behav Original Research BACKGROUND: Paired associative stimulation (PAS) is widely used to induce plasticity in the human motor cortex. Although reciprocal inhibition of antagonist muscles plays a fundamental role in human movements, change in cortical circuits for reciprocal muscles by PAS is unknown. METHODS: We investigated change in cortical plasticity for reciprocal muscles during PAS. PAS consisted of 200 pairs of peripheral electric stimulation of the right median nerve at the wrist at a frequency of 0.25 Hz followed by transcranial magnetic stimulation of the left M1 at the midpoint between the center of gravities of the flexor carpi radialis (FCR) and extensor carpi radialis (ECR) muscles. Measures of motor cortical excitability included resting motor threshold (RMT), GABA(A)-mediated short-interval intracortical inhibition (SICI), and GABA(B)-mediated long-interval intracortical inhibition (LICI). RESULTS: Motor evoked potential amplitude-conditioned LICI for the FCR muscle was significantly decreased after PAS (P = 0.020), whereas that for the ECR muscle was significantly increased (P = 0.033). Changes in RMT and SICI for the FCR and ECR muscles were not significantly different before and after PAS. Corticospinal excitability for both reciprocal muscles was increased during PAS, but GABA(B)-mediated cortical inhibitory functions for the agonist and antagonist muscles were reciprocally altered after PAS. CONCLUSION: These results implied that the cortical excitability for reciprocal muscles including GABA(B)-ergic inhibitory systems within human M1 could be differently altered by PAS. BlackWell Publishing Ltd 2014-11 2014-10-15 /pmc/articles/PMC4212109/ /pubmed/25365805 http://dx.doi.org/10.1002/brb3.280 Text en © 2014 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Suzuki, Makoto
Kirimoto, Hikari
Sugawara, Kazuhiro
Watanabe, Makoto
Shimizu, Shinobu
Ishizaka, Ikuyo
Yamada, Sumio
Matsunaga, Atsuhiko
Fukuda, Michinari
Onishi, Hideaki
Induction of cortical plasticity for reciprocal muscles by paired associative stimulation
title Induction of cortical plasticity for reciprocal muscles by paired associative stimulation
title_full Induction of cortical plasticity for reciprocal muscles by paired associative stimulation
title_fullStr Induction of cortical plasticity for reciprocal muscles by paired associative stimulation
title_full_unstemmed Induction of cortical plasticity for reciprocal muscles by paired associative stimulation
title_short Induction of cortical plasticity for reciprocal muscles by paired associative stimulation
title_sort induction of cortical plasticity for reciprocal muscles by paired associative stimulation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212109/
https://www.ncbi.nlm.nih.gov/pubmed/25365805
http://dx.doi.org/10.1002/brb3.280
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