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Transspinal Direct Current Stimulation Produces Persistent Plasticity in Human Motor Pathways
The spinal cord is an integration center for descending, ascending, and segmental neural signals. Noninvasive transspinal stimulation may thus constitute an effective method for concomitant modulation of local and distal neural circuits. In this study, we established changes in cortical excitability...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768745/ https://www.ncbi.nlm.nih.gov/pubmed/29335430 http://dx.doi.org/10.1038/s41598-017-18872-z |
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author | Murray, Lynda M. Tahayori, Behdad Knikou, Maria |
author_facet | Murray, Lynda M. Tahayori, Behdad Knikou, Maria |
author_sort | Murray, Lynda M. |
collection | PubMed |
description | The spinal cord is an integration center for descending, ascending, and segmental neural signals. Noninvasive transspinal stimulation may thus constitute an effective method for concomitant modulation of local and distal neural circuits. In this study, we established changes in cortical excitability and input/output function of corticospinal and spinal neural circuits before, at 0–15 and at 30–45 minutes after cathodal, anodal, and sham transspinal direct current stimulation (tsDCS) to the thoracic region in healthy individuals. We found that intracortical inhibition was different among stimulation polarities, however remained unchanged over time. Intracortical facilitation increased after cathodal and anodal tsDCS delivered with subjects seated, and decreased after cathodal tsDCS delivered with subjects lying supine. Both cathodal and anodal tsDCS increased corticospinal excitability, yet facilitation was larger and persisted for 30 minutes post stimulation only when cathodal tsDCS was delivered with subjects lying supine. Spinal input/output reflex function was decreased by cathodal and not anodal tsDCS. These changes may be attributed to altered spontaneous neural activity and membrane potentials of corticomotoneuronal cells by tsDCS involving similar mechanisms to those mediating motor learning. Our findings indicate that thoracic tsDCS has the ability to concomitantly alter cortical, corticospinal, and spinal motor output in humans. |
format | Online Article Text |
id | pubmed-5768745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57687452018-01-25 Transspinal Direct Current Stimulation Produces Persistent Plasticity in Human Motor Pathways Murray, Lynda M. Tahayori, Behdad Knikou, Maria Sci Rep Article The spinal cord is an integration center for descending, ascending, and segmental neural signals. Noninvasive transspinal stimulation may thus constitute an effective method for concomitant modulation of local and distal neural circuits. In this study, we established changes in cortical excitability and input/output function of corticospinal and spinal neural circuits before, at 0–15 and at 30–45 minutes after cathodal, anodal, and sham transspinal direct current stimulation (tsDCS) to the thoracic region in healthy individuals. We found that intracortical inhibition was different among stimulation polarities, however remained unchanged over time. Intracortical facilitation increased after cathodal and anodal tsDCS delivered with subjects seated, and decreased after cathodal tsDCS delivered with subjects lying supine. Both cathodal and anodal tsDCS increased corticospinal excitability, yet facilitation was larger and persisted for 30 minutes post stimulation only when cathodal tsDCS was delivered with subjects lying supine. Spinal input/output reflex function was decreased by cathodal and not anodal tsDCS. These changes may be attributed to altered spontaneous neural activity and membrane potentials of corticomotoneuronal cells by tsDCS involving similar mechanisms to those mediating motor learning. Our findings indicate that thoracic tsDCS has the ability to concomitantly alter cortical, corticospinal, and spinal motor output in humans. Nature Publishing Group UK 2018-01-15 /pmc/articles/PMC5768745/ /pubmed/29335430 http://dx.doi.org/10.1038/s41598-017-18872-z Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Murray, Lynda M. Tahayori, Behdad Knikou, Maria Transspinal Direct Current Stimulation Produces Persistent Plasticity in Human Motor Pathways |
title | Transspinal Direct Current Stimulation Produces Persistent Plasticity in Human Motor Pathways |
title_full | Transspinal Direct Current Stimulation Produces Persistent Plasticity in Human Motor Pathways |
title_fullStr | Transspinal Direct Current Stimulation Produces Persistent Plasticity in Human Motor Pathways |
title_full_unstemmed | Transspinal Direct Current Stimulation Produces Persistent Plasticity in Human Motor Pathways |
title_short | Transspinal Direct Current Stimulation Produces Persistent Plasticity in Human Motor Pathways |
title_sort | transspinal direct current stimulation produces persistent plasticity in human motor pathways |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768745/ https://www.ncbi.nlm.nih.gov/pubmed/29335430 http://dx.doi.org/10.1038/s41598-017-18872-z |
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