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Effects of active and sham tDCS on the soleus H-reflex during standing

Weak transcranial direct current stimulation (tDCS) is known to affect corticospinal excitability and enhance motor skill acquisition, whereas its effects on spinal reflexes in actively contracting muscles are yet to be established. Thus, in this study, we examined the acute effects of Active and Sh...

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Autores principales: McCane, Lynn M., Wolpaw, Jonathan R., Thompson, Aiko K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10224818/
https://www.ncbi.nlm.nih.gov/pubmed/37145136
http://dx.doi.org/10.1007/s00221-023-06624-7
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author McCane, Lynn M.
Wolpaw, Jonathan R.
Thompson, Aiko K.
author_facet McCane, Lynn M.
Wolpaw, Jonathan R.
Thompson, Aiko K.
author_sort McCane, Lynn M.
collection PubMed
description Weak transcranial direct current stimulation (tDCS) is known to affect corticospinal excitability and enhance motor skill acquisition, whereas its effects on spinal reflexes in actively contracting muscles are yet to be established. Thus, in this study, we examined the acute effects of Active and Sham tDCS on the soleus H-reflex during standing. In fourteen adults without known neurological conditions, the soleus H-reflex was repeatedly elicited at just above M-wave threshold throughout 30 min of Active (N = 7) or Sham (N = 7) 2-mA tDCS over the primary motor cortex in standing. The maximum H-reflex (H(max)) and M-wave (M(max)) were also measured before and immediately after 30 min of tDCS. The soleus H-reflex amplitudes became significantly larger (by 6%) ≈1 min into Active or Sham tDCS and gradually returned toward the pre-tDCS values, on average, within 15 min. With Active tDCS, the amplitude reduction from the initial increase appeared to occur more swiftly than with Sham tDCS. An acute temporary increase in the soleus H-reflex amplitude within the first minute of Active and Sham tDCS found in this study indicates a previously unreported effect of tDCS on the H-reflex excitability. The present study suggests that neurophysiological characterization of Sham tDCS effects is just as important as investigating Active tDCS effects in understanding and defining acute effects of tDCS on the excitability of spinal reflex pathways.
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spelling pubmed-102248182023-05-29 Effects of active and sham tDCS on the soleus H-reflex during standing McCane, Lynn M. Wolpaw, Jonathan R. Thompson, Aiko K. Exp Brain Res Research Article Weak transcranial direct current stimulation (tDCS) is known to affect corticospinal excitability and enhance motor skill acquisition, whereas its effects on spinal reflexes in actively contracting muscles are yet to be established. Thus, in this study, we examined the acute effects of Active and Sham tDCS on the soleus H-reflex during standing. In fourteen adults without known neurological conditions, the soleus H-reflex was repeatedly elicited at just above M-wave threshold throughout 30 min of Active (N = 7) or Sham (N = 7) 2-mA tDCS over the primary motor cortex in standing. The maximum H-reflex (H(max)) and M-wave (M(max)) were also measured before and immediately after 30 min of tDCS. The soleus H-reflex amplitudes became significantly larger (by 6%) ≈1 min into Active or Sham tDCS and gradually returned toward the pre-tDCS values, on average, within 15 min. With Active tDCS, the amplitude reduction from the initial increase appeared to occur more swiftly than with Sham tDCS. An acute temporary increase in the soleus H-reflex amplitude within the first minute of Active and Sham tDCS found in this study indicates a previously unreported effect of tDCS on the H-reflex excitability. The present study suggests that neurophysiological characterization of Sham tDCS effects is just as important as investigating Active tDCS effects in understanding and defining acute effects of tDCS on the excitability of spinal reflex pathways. Springer Berlin Heidelberg 2023-05-05 2023 /pmc/articles/PMC10224818/ /pubmed/37145136 http://dx.doi.org/10.1007/s00221-023-06624-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Research Article
McCane, Lynn M.
Wolpaw, Jonathan R.
Thompson, Aiko K.
Effects of active and sham tDCS on the soleus H-reflex during standing
title Effects of active and sham tDCS on the soleus H-reflex during standing
title_full Effects of active and sham tDCS on the soleus H-reflex during standing
title_fullStr Effects of active and sham tDCS on the soleus H-reflex during standing
title_full_unstemmed Effects of active and sham tDCS on the soleus H-reflex during standing
title_short Effects of active and sham tDCS on the soleus H-reflex during standing
title_sort effects of active and sham tdcs on the soleus h-reflex during standing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10224818/
https://www.ncbi.nlm.nih.gov/pubmed/37145136
http://dx.doi.org/10.1007/s00221-023-06624-7
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