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Investigating Cerebellar Modulation of Premovement Beta-Band Activity during Motor Adaptation †

Enhancing cerebellar activity influences motor cortical activity and contributes to motor adaptation, though it is unclear which neurophysiological mechanisms contributing to adaptation are influenced by the cerebellum. Pre-movement beta event-related desynchronization (β-ERD), which reflects a rele...

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Autores principales: Kaethler, Lynea B., Brown, Katlyn E., Meehan, Sean K., Staines, W. Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669216/
https://www.ncbi.nlm.nih.gov/pubmed/38002483
http://dx.doi.org/10.3390/brainsci13111523
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author Kaethler, Lynea B.
Brown, Katlyn E.
Meehan, Sean K.
Staines, W. Richard
author_facet Kaethler, Lynea B.
Brown, Katlyn E.
Meehan, Sean K.
Staines, W. Richard
author_sort Kaethler, Lynea B.
collection PubMed
description Enhancing cerebellar activity influences motor cortical activity and contributes to motor adaptation, though it is unclear which neurophysiological mechanisms contributing to adaptation are influenced by the cerebellum. Pre-movement beta event-related desynchronization (β-ERD), which reflects a release of inhibitory control in the premotor cortex during movement planning, is one mechanism that may be modulated by the cerebellum through cerebellar-premotor connections. We hypothesized that enhancing cerebellar activity with intermittent theta burst stimulation (iTBS) would improve adaptation rates and increase β-ERD during motor adaptation. Thirty-four participants were randomly assigned to an active (A-iTBS) or sham cerebellar iTBS (S-iTBS) group. Participants performed a visuomotor task, using a joystick to move a cursor to targets, prior to receiving A-iTBS or S-iTBS, following which they completed training with a 45° rotation to the cursor movement. Behavioural adaptation was assessed using the angular error of the cursor path relative to the ideal trajectory. The results showed a greater adaptation rate following A-iTBS and an increase in β-ERD, specific to the high β range (20–30 Hz) during motor planning, compared to S-iTBS, indicative of cerebellar modulation of the motor cortical inhibitory control network. The enhanced release of inhibitory activity persisted throughout training, which suggests that the cerebellar influence over the premotor cortex extends beyond adaptation to other stages of motor learning. The results from this study further understanding of cerebellum-motor connections as they relate to acquiring motor skills and may inform future skill training and rehabilitation protocols.
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spelling pubmed-106692162023-10-28 Investigating Cerebellar Modulation of Premovement Beta-Band Activity during Motor Adaptation † Kaethler, Lynea B. Brown, Katlyn E. Meehan, Sean K. Staines, W. Richard Brain Sci Article Enhancing cerebellar activity influences motor cortical activity and contributes to motor adaptation, though it is unclear which neurophysiological mechanisms contributing to adaptation are influenced by the cerebellum. Pre-movement beta event-related desynchronization (β-ERD), which reflects a release of inhibitory control in the premotor cortex during movement planning, is one mechanism that may be modulated by the cerebellum through cerebellar-premotor connections. We hypothesized that enhancing cerebellar activity with intermittent theta burst stimulation (iTBS) would improve adaptation rates and increase β-ERD during motor adaptation. Thirty-four participants were randomly assigned to an active (A-iTBS) or sham cerebellar iTBS (S-iTBS) group. Participants performed a visuomotor task, using a joystick to move a cursor to targets, prior to receiving A-iTBS or S-iTBS, following which they completed training with a 45° rotation to the cursor movement. Behavioural adaptation was assessed using the angular error of the cursor path relative to the ideal trajectory. The results showed a greater adaptation rate following A-iTBS and an increase in β-ERD, specific to the high β range (20–30 Hz) during motor planning, compared to S-iTBS, indicative of cerebellar modulation of the motor cortical inhibitory control network. The enhanced release of inhibitory activity persisted throughout training, which suggests that the cerebellar influence over the premotor cortex extends beyond adaptation to other stages of motor learning. The results from this study further understanding of cerebellum-motor connections as they relate to acquiring motor skills and may inform future skill training and rehabilitation protocols. MDPI 2023-10-28 /pmc/articles/PMC10669216/ /pubmed/38002483 http://dx.doi.org/10.3390/brainsci13111523 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kaethler, Lynea B.
Brown, Katlyn E.
Meehan, Sean K.
Staines, W. Richard
Investigating Cerebellar Modulation of Premovement Beta-Band Activity during Motor Adaptation †
title Investigating Cerebellar Modulation of Premovement Beta-Band Activity during Motor Adaptation †
title_full Investigating Cerebellar Modulation of Premovement Beta-Band Activity during Motor Adaptation †
title_fullStr Investigating Cerebellar Modulation of Premovement Beta-Band Activity during Motor Adaptation †
title_full_unstemmed Investigating Cerebellar Modulation of Premovement Beta-Band Activity during Motor Adaptation †
title_short Investigating Cerebellar Modulation of Premovement Beta-Band Activity during Motor Adaptation †
title_sort investigating cerebellar modulation of premovement beta-band activity during motor adaptation †
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669216/
https://www.ncbi.nlm.nih.gov/pubmed/38002483
http://dx.doi.org/10.3390/brainsci13111523
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