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(1)H MR spectroscopy of the motor cortex immediately following transcranial direct current stimulation at 7 Tesla

Transcranial direct current stimulation (tDCS) is a form of non-invasive brain stimulation that may modulate cortical excitability, metabolite concentration, and human behaviour. The supplementary motor area (SMA) has been largely ignored as a potential target for tDCS neurorehabilitation but is an...

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Autores principales: Ryan, Kayla, Wawrzyn, Krzysztof, Gati, Joseph S., Chronik, Blaine A., Wong, Dickson, Duggal, Neil, Bartha, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114283/
https://www.ncbi.nlm.nih.gov/pubmed/30157179
http://dx.doi.org/10.1371/journal.pone.0198053
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author Ryan, Kayla
Wawrzyn, Krzysztof
Gati, Joseph S.
Chronik, Blaine A.
Wong, Dickson
Duggal, Neil
Bartha, Robert
author_facet Ryan, Kayla
Wawrzyn, Krzysztof
Gati, Joseph S.
Chronik, Blaine A.
Wong, Dickson
Duggal, Neil
Bartha, Robert
author_sort Ryan, Kayla
collection PubMed
description Transcranial direct current stimulation (tDCS) is a form of non-invasive brain stimulation that may modulate cortical excitability, metabolite concentration, and human behaviour. The supplementary motor area (SMA) has been largely ignored as a potential target for tDCS neurorehabilitation but is an important region in motor compensation after brain injury with strong efferent connections to the primary motor cortex (M1). The objective of this work was to measure tissue metabolite changes in the human motor cortex immediately following tDCS. We hypothesized that bihemispheric tDCS would change levels of metabolites involved in neuromodulation including N-acetylaspartate (NAA), glutamate (Glu), and creatine (tCr). In this single-blind, randomized, cross-over study, fifteen healthy adults aged 21–60 participated in two 7T MRI sessions, to identify changes in metabolite concentrations by magnetic resonance spectroscopy. Immediately after 20 minutes of tDCS, there were no significant changes in metabolite levels or metabolite ratios comparing tDCS to sham. However there was a trend toward increased NAA/tCr concentration (p = 0.08) in M1 under the stimulating cathode. There was a strong, positive correlation between the change in the absolute concentration of NAA and the change in the absolute concentration of tCr (p<0.001) suggesting an effect of tDCS. Both NAA and creatine are important markers of neurometabolism. Our findings provide novel insight into the modulation of neural metabolites in the motor cortex immediately following application of bihemispheric tDCS.
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spelling pubmed-61142832018-09-17 (1)H MR spectroscopy of the motor cortex immediately following transcranial direct current stimulation at 7 Tesla Ryan, Kayla Wawrzyn, Krzysztof Gati, Joseph S. Chronik, Blaine A. Wong, Dickson Duggal, Neil Bartha, Robert PLoS One Research Article Transcranial direct current stimulation (tDCS) is a form of non-invasive brain stimulation that may modulate cortical excitability, metabolite concentration, and human behaviour. The supplementary motor area (SMA) has been largely ignored as a potential target for tDCS neurorehabilitation but is an important region in motor compensation after brain injury with strong efferent connections to the primary motor cortex (M1). The objective of this work was to measure tissue metabolite changes in the human motor cortex immediately following tDCS. We hypothesized that bihemispheric tDCS would change levels of metabolites involved in neuromodulation including N-acetylaspartate (NAA), glutamate (Glu), and creatine (tCr). In this single-blind, randomized, cross-over study, fifteen healthy adults aged 21–60 participated in two 7T MRI sessions, to identify changes in metabolite concentrations by magnetic resonance spectroscopy. Immediately after 20 minutes of tDCS, there were no significant changes in metabolite levels or metabolite ratios comparing tDCS to sham. However there was a trend toward increased NAA/tCr concentration (p = 0.08) in M1 under the stimulating cathode. There was a strong, positive correlation between the change in the absolute concentration of NAA and the change in the absolute concentration of tCr (p<0.001) suggesting an effect of tDCS. Both NAA and creatine are important markers of neurometabolism. Our findings provide novel insight into the modulation of neural metabolites in the motor cortex immediately following application of bihemispheric tDCS. Public Library of Science 2018-08-29 /pmc/articles/PMC6114283/ /pubmed/30157179 http://dx.doi.org/10.1371/journal.pone.0198053 Text en © 2018 Ryan et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ryan, Kayla
Wawrzyn, Krzysztof
Gati, Joseph S.
Chronik, Blaine A.
Wong, Dickson
Duggal, Neil
Bartha, Robert
(1)H MR spectroscopy of the motor cortex immediately following transcranial direct current stimulation at 7 Tesla
title (1)H MR spectroscopy of the motor cortex immediately following transcranial direct current stimulation at 7 Tesla
title_full (1)H MR spectroscopy of the motor cortex immediately following transcranial direct current stimulation at 7 Tesla
title_fullStr (1)H MR spectroscopy of the motor cortex immediately following transcranial direct current stimulation at 7 Tesla
title_full_unstemmed (1)H MR spectroscopy of the motor cortex immediately following transcranial direct current stimulation at 7 Tesla
title_short (1)H MR spectroscopy of the motor cortex immediately following transcranial direct current stimulation at 7 Tesla
title_sort (1)h mr spectroscopy of the motor cortex immediately following transcranial direct current stimulation at 7 tesla
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114283/
https://www.ncbi.nlm.nih.gov/pubmed/30157179
http://dx.doi.org/10.1371/journal.pone.0198053
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