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Transcutaneous spinal direct current stimulation increases corticospinal transmission and enhances voluntary motor output in humans

Optimization of motor performance is of importance in daily life, in relation to recovery following injury as well as for elite sports performance. The present study investigated whether transcutaneous spinal direct current stimulation (tsDCS) may enhance voluntary ballistic activation of ankle musc...

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Autores principales: Yamaguchi, Tomofumi, Beck, Mikkel M., Therkildsen, Eva R., Svane, Christian, Forman, Christian, Lorentzen, Jakob, Conway, Bernard A., Lundbye‐Jensen, Jesper, Geertsen, Svend S., Nielsen, Jens B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435034/
https://www.ncbi.nlm.nih.gov/pubmed/32812363
http://dx.doi.org/10.14814/phy2.14531
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author Yamaguchi, Tomofumi
Beck, Mikkel M.
Therkildsen, Eva R.
Svane, Christian
Forman, Christian
Lorentzen, Jakob
Conway, Bernard A.
Lundbye‐Jensen, Jesper
Geertsen, Svend S.
Nielsen, Jens B.
author_facet Yamaguchi, Tomofumi
Beck, Mikkel M.
Therkildsen, Eva R.
Svane, Christian
Forman, Christian
Lorentzen, Jakob
Conway, Bernard A.
Lundbye‐Jensen, Jesper
Geertsen, Svend S.
Nielsen, Jens B.
author_sort Yamaguchi, Tomofumi
collection PubMed
description Optimization of motor performance is of importance in daily life, in relation to recovery following injury as well as for elite sports performance. The present study investigated whether transcutaneous spinal direct current stimulation (tsDCS) may enhance voluntary ballistic activation of ankle muscles and descending activation of spinal motor neurons in able‐bodied adults. Forty‐one adults (21 men; 24.0 ± 3.2 years) participated in the study. The effect of tsDCS on ballistic motor performance and plantar flexor muscle activation was assessed in a double‐blinded sham‐controlled cross‐over experiment. In separate experiments, the underlying changes in excitability of corticospinal and spinal pathways were probed by evaluating soleus (SOL) motor evoked potentials (MEPs) following single‐pulse transcranial magnetic stimulation (TMS) over the primary motor cortex, SOL H‐reflexes elicited by tibial nerve stimulation and TMS‐conditioning of SOL H‐reflexes. Measures were obtained before and after cathodal tsDCS over the thoracic spine (T11‐T12) for 10 min at 2.5 mA. We found that cathodal tsDCS transiently facilitated peak acceleration in the ballistic motor task compared to sham tsDCS. Following tsDCS, SOL MEPs were increased without changes in H‐reflex amplitudes. The short‐latency facilitation of the H‐reflex by subthreshold TMS, which is assumed to be mediated by the fast conducting monosynaptic corticomotoneuronal pathway, was also enhanced by tsDCS. We argue that tsDCS briefly facilitates voluntary motor output by increasing descending drive from corticospinal neurones to spinal plantar flexor motor neurons. tsDCS can thus transiently promote within‐session CNS function and voluntary motor output and holds potential as a technique in the rehabilitation of motor function following central nervous lesions.
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spelling pubmed-74350342020-08-20 Transcutaneous spinal direct current stimulation increases corticospinal transmission and enhances voluntary motor output in humans Yamaguchi, Tomofumi Beck, Mikkel M. Therkildsen, Eva R. Svane, Christian Forman, Christian Lorentzen, Jakob Conway, Bernard A. Lundbye‐Jensen, Jesper Geertsen, Svend S. Nielsen, Jens B. Physiol Rep Original Research Optimization of motor performance is of importance in daily life, in relation to recovery following injury as well as for elite sports performance. The present study investigated whether transcutaneous spinal direct current stimulation (tsDCS) may enhance voluntary ballistic activation of ankle muscles and descending activation of spinal motor neurons in able‐bodied adults. Forty‐one adults (21 men; 24.0 ± 3.2 years) participated in the study. The effect of tsDCS on ballistic motor performance and plantar flexor muscle activation was assessed in a double‐blinded sham‐controlled cross‐over experiment. In separate experiments, the underlying changes in excitability of corticospinal and spinal pathways were probed by evaluating soleus (SOL) motor evoked potentials (MEPs) following single‐pulse transcranial magnetic stimulation (TMS) over the primary motor cortex, SOL H‐reflexes elicited by tibial nerve stimulation and TMS‐conditioning of SOL H‐reflexes. Measures were obtained before and after cathodal tsDCS over the thoracic spine (T11‐T12) for 10 min at 2.5 mA. We found that cathodal tsDCS transiently facilitated peak acceleration in the ballistic motor task compared to sham tsDCS. Following tsDCS, SOL MEPs were increased without changes in H‐reflex amplitudes. The short‐latency facilitation of the H‐reflex by subthreshold TMS, which is assumed to be mediated by the fast conducting monosynaptic corticomotoneuronal pathway, was also enhanced by tsDCS. We argue that tsDCS briefly facilitates voluntary motor output by increasing descending drive from corticospinal neurones to spinal plantar flexor motor neurons. tsDCS can thus transiently promote within‐session CNS function and voluntary motor output and holds potential as a technique in the rehabilitation of motor function following central nervous lesions. John Wiley and Sons Inc. 2020-08-18 /pmc/articles/PMC7435034/ /pubmed/32812363 http://dx.doi.org/10.14814/phy2.14531 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Yamaguchi, Tomofumi
Beck, Mikkel M.
Therkildsen, Eva R.
Svane, Christian
Forman, Christian
Lorentzen, Jakob
Conway, Bernard A.
Lundbye‐Jensen, Jesper
Geertsen, Svend S.
Nielsen, Jens B.
Transcutaneous spinal direct current stimulation increases corticospinal transmission and enhances voluntary motor output in humans
title Transcutaneous spinal direct current stimulation increases corticospinal transmission and enhances voluntary motor output in humans
title_full Transcutaneous spinal direct current stimulation increases corticospinal transmission and enhances voluntary motor output in humans
title_fullStr Transcutaneous spinal direct current stimulation increases corticospinal transmission and enhances voluntary motor output in humans
title_full_unstemmed Transcutaneous spinal direct current stimulation increases corticospinal transmission and enhances voluntary motor output in humans
title_short Transcutaneous spinal direct current stimulation increases corticospinal transmission and enhances voluntary motor output in humans
title_sort transcutaneous spinal direct current stimulation increases corticospinal transmission and enhances voluntary motor output in humans
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435034/
https://www.ncbi.nlm.nih.gov/pubmed/32812363
http://dx.doi.org/10.14814/phy2.14531
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