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Modulations of corticospinal excitability following rapid ankle dorsiflexion in skill- and endurance-trained athletes

PURPOSE: Long-term sports training, such as skill and endurance training, leads to specific neuroplasticity. However, it remains unclear if muscle stretch-induced proprioceptive feedback influences corticospinal facilitation/inhibition differently between skill- and endurance-trained athletes. This...

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Autores principales: Hu, Nijia, Avela, Janne, Kidgell, Dawson J., Piirainen, Jarmo M., Walker, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9212199/
https://www.ncbi.nlm.nih.gov/pubmed/35729431
http://dx.doi.org/10.1007/s00421-022-04981-9
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author Hu, Nijia
Avela, Janne
Kidgell, Dawson J.
Piirainen, Jarmo M.
Walker, Simon
author_facet Hu, Nijia
Avela, Janne
Kidgell, Dawson J.
Piirainen, Jarmo M.
Walker, Simon
author_sort Hu, Nijia
collection PubMed
description PURPOSE: Long-term sports training, such as skill and endurance training, leads to specific neuroplasticity. However, it remains unclear if muscle stretch-induced proprioceptive feedback influences corticospinal facilitation/inhibition differently between skill- and endurance-trained athletes. This study investigated modulation of corticospinal excitability following rapid ankle dorsiflexion between well-trained skill and endurance athletes. METHODS: Ten skill- and ten endurance-trained athletes participated in the study. Corticospinal excitability was tested by single- and paired-pulse transcranial magnetic stimulations (TMS) at three different latencies following passive rapid ankle dorsiflexion. Motor evoked potential (MEP), short-latency intracortical inhibition (SICI), intracortical facilitation (ICF), and long-latency intracortical inhibition (LICI) were recorded by surface electromyography from the soleus muscle. RESULTS: Compared to immediately before ankle dorsiflexion (Onset), TMS induced significantly greater MEPs during the supraspinal reaction period (~ 120 ms after short-latency reflex, SLR) in the skill group only (from 1.7 ± 1.0 to 2.7 ± 1.8%M-max, P = 0.005) despite both conditions being passive. ICF was significantly greater over all latencies in skill than endurance athletes (F ((3, 45)) = 4.64, P = 0.007), although no between-group differences for stimulations at specific latencies (e.g., at SLR) were observed. CONCLUSION: The skill group showed higher corticospinal excitability during the supraspinal reaction phase, which may indicate a “priming” of corticospinal excitability following rapid ankle dorsiflexion for a supraspinal reaction post-stretch, which appears absent in endurance-trained athletes.
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spelling pubmed-92121992022-06-22 Modulations of corticospinal excitability following rapid ankle dorsiflexion in skill- and endurance-trained athletes Hu, Nijia Avela, Janne Kidgell, Dawson J. Piirainen, Jarmo M. Walker, Simon Eur J Appl Physiol Original Article PURPOSE: Long-term sports training, such as skill and endurance training, leads to specific neuroplasticity. However, it remains unclear if muscle stretch-induced proprioceptive feedback influences corticospinal facilitation/inhibition differently between skill- and endurance-trained athletes. This study investigated modulation of corticospinal excitability following rapid ankle dorsiflexion between well-trained skill and endurance athletes. METHODS: Ten skill- and ten endurance-trained athletes participated in the study. Corticospinal excitability was tested by single- and paired-pulse transcranial magnetic stimulations (TMS) at three different latencies following passive rapid ankle dorsiflexion. Motor evoked potential (MEP), short-latency intracortical inhibition (SICI), intracortical facilitation (ICF), and long-latency intracortical inhibition (LICI) were recorded by surface electromyography from the soleus muscle. RESULTS: Compared to immediately before ankle dorsiflexion (Onset), TMS induced significantly greater MEPs during the supraspinal reaction period (~ 120 ms after short-latency reflex, SLR) in the skill group only (from 1.7 ± 1.0 to 2.7 ± 1.8%M-max, P = 0.005) despite both conditions being passive. ICF was significantly greater over all latencies in skill than endurance athletes (F ((3, 45)) = 4.64, P = 0.007), although no between-group differences for stimulations at specific latencies (e.g., at SLR) were observed. CONCLUSION: The skill group showed higher corticospinal excitability during the supraspinal reaction phase, which may indicate a “priming” of corticospinal excitability following rapid ankle dorsiflexion for a supraspinal reaction post-stretch, which appears absent in endurance-trained athletes. Springer Berlin Heidelberg 2022-06-21 2022 /pmc/articles/PMC9212199/ /pubmed/35729431 http://dx.doi.org/10.1007/s00421-022-04981-9 Text en © The Author(s) 2022 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 Original Article
Hu, Nijia
Avela, Janne
Kidgell, Dawson J.
Piirainen, Jarmo M.
Walker, Simon
Modulations of corticospinal excitability following rapid ankle dorsiflexion in skill- and endurance-trained athletes
title Modulations of corticospinal excitability following rapid ankle dorsiflexion in skill- and endurance-trained athletes
title_full Modulations of corticospinal excitability following rapid ankle dorsiflexion in skill- and endurance-trained athletes
title_fullStr Modulations of corticospinal excitability following rapid ankle dorsiflexion in skill- and endurance-trained athletes
title_full_unstemmed Modulations of corticospinal excitability following rapid ankle dorsiflexion in skill- and endurance-trained athletes
title_short Modulations of corticospinal excitability following rapid ankle dorsiflexion in skill- and endurance-trained athletes
title_sort modulations of corticospinal excitability following rapid ankle dorsiflexion in skill- and endurance-trained athletes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9212199/
https://www.ncbi.nlm.nih.gov/pubmed/35729431
http://dx.doi.org/10.1007/s00421-022-04981-9
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