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Short-interval intracortical inhibition and facilitation targeting upper and lower limb muscles

Transcranial magnetic stimulation (TMS) can be used to study excitability of corticospinal neurons in human motor cortex. It is currently not fully elucidated if corticospinal neurons in the hand vs. leg representation show the same or different regulation of their excitability by GABAAergic and glu...

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Autores principales: Mrachacz-Kersting, Natalie, Stevenson, Andrew James Thomas, Ziemann, Ulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578654/
https://www.ncbi.nlm.nih.gov/pubmed/34754010
http://dx.doi.org/10.1038/s41598-021-01348-6
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author Mrachacz-Kersting, Natalie
Stevenson, Andrew James Thomas
Ziemann, Ulf
author_facet Mrachacz-Kersting, Natalie
Stevenson, Andrew James Thomas
Ziemann, Ulf
author_sort Mrachacz-Kersting, Natalie
collection PubMed
description Transcranial magnetic stimulation (TMS) can be used to study excitability of corticospinal neurons in human motor cortex. It is currently not fully elucidated if corticospinal neurons in the hand vs. leg representation show the same or different regulation of their excitability by GABAAergic and glutamatergic interneuronal circuitry. Using a paired-pulse TMS protocol we tested short-interval intracortical inhibition (SICI) and short-interval intracortical facilitation (SICF) in 18 healthy participants. Motor evoked potentials were evoked in one hand (abductor digiti minimi) and one leg muscle (tibialis anterior), with systematic variation of the intensities of the first (S1) and second (S2) pulse between 60 and 140% resting motor threshold (RMT) in 10% steps, at two interstimulus intervals of 1.5 and 2.1 ms. For the hand and leg motor representations and for both interstimulus intervals, SICI occurred if the intensities of S1 < RMT and S2 > RMT, while SICF predominated if S1 = S2 ≤ RMT, or S1 > RMT and S2 < RMT. Findings confirm and extend previous evidence that the regulation of excitability of corticospinal neurons of the hand versus leg representation in human primary cortex through GABAAergic and glutamatergic interneuronal circuits is highly similar, and that corticospinal neurons of both representations are activated by TMS transsynaptically in largely identical ways.
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spelling pubmed-85786542021-11-10 Short-interval intracortical inhibition and facilitation targeting upper and lower limb muscles Mrachacz-Kersting, Natalie Stevenson, Andrew James Thomas Ziemann, Ulf Sci Rep Article Transcranial magnetic stimulation (TMS) can be used to study excitability of corticospinal neurons in human motor cortex. It is currently not fully elucidated if corticospinal neurons in the hand vs. leg representation show the same or different regulation of their excitability by GABAAergic and glutamatergic interneuronal circuitry. Using a paired-pulse TMS protocol we tested short-interval intracortical inhibition (SICI) and short-interval intracortical facilitation (SICF) in 18 healthy participants. Motor evoked potentials were evoked in one hand (abductor digiti minimi) and one leg muscle (tibialis anterior), with systematic variation of the intensities of the first (S1) and second (S2) pulse between 60 and 140% resting motor threshold (RMT) in 10% steps, at two interstimulus intervals of 1.5 and 2.1 ms. For the hand and leg motor representations and for both interstimulus intervals, SICI occurred if the intensities of S1 < RMT and S2 > RMT, while SICF predominated if S1 = S2 ≤ RMT, or S1 > RMT and S2 < RMT. Findings confirm and extend previous evidence that the regulation of excitability of corticospinal neurons of the hand versus leg representation in human primary cortex through GABAAergic and glutamatergic interneuronal circuits is highly similar, and that corticospinal neurons of both representations are activated by TMS transsynaptically in largely identical ways. Nature Publishing Group UK 2021-11-09 /pmc/articles/PMC8578654/ /pubmed/34754010 http://dx.doi.org/10.1038/s41598-021-01348-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mrachacz-Kersting, Natalie
Stevenson, Andrew James Thomas
Ziemann, Ulf
Short-interval intracortical inhibition and facilitation targeting upper and lower limb muscles
title Short-interval intracortical inhibition and facilitation targeting upper and lower limb muscles
title_full Short-interval intracortical inhibition and facilitation targeting upper and lower limb muscles
title_fullStr Short-interval intracortical inhibition and facilitation targeting upper and lower limb muscles
title_full_unstemmed Short-interval intracortical inhibition and facilitation targeting upper and lower limb muscles
title_short Short-interval intracortical inhibition and facilitation targeting upper and lower limb muscles
title_sort short-interval intracortical inhibition and facilitation targeting upper and lower limb muscles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578654/
https://www.ncbi.nlm.nih.gov/pubmed/34754010
http://dx.doi.org/10.1038/s41598-021-01348-6
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