Cargando…

Body Sway Increases After Functional Inactivation of the Cerebellar Vermis by cTBS

Balance stability correlates with cerebellar vermis volume. Furthermore, the cerebellum is involved in precise timing of motor processes by fine-tuning the sensorimotor integration. We tested the hypothesis that any cerebellar action in stance control and in timing of visuomotor integration for bala...

Descripción completa

Detalles Bibliográficos
Autores principales: Colnaghi, Silvia, Honeine, Jean-Louis, Sozzi, Stefania, Schieppati, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243877/
https://www.ncbi.nlm.nih.gov/pubmed/26780373
http://dx.doi.org/10.1007/s12311-015-0758-5
_version_ 1782496594249121792
author Colnaghi, Silvia
Honeine, Jean-Louis
Sozzi, Stefania
Schieppati, Marco
author_facet Colnaghi, Silvia
Honeine, Jean-Louis
Sozzi, Stefania
Schieppati, Marco
author_sort Colnaghi, Silvia
collection PubMed
description Balance stability correlates with cerebellar vermis volume. Furthermore, the cerebellum is involved in precise timing of motor processes by fine-tuning the sensorimotor integration. We tested the hypothesis that any cerebellar action in stance control and in timing of visuomotor integration for balance is impaired by continuous theta-burst stimulation (cTBS) of the vermis. Ten subjects stood quietly and underwent six sequences of 10-min acquisition of center of foot pressure (CoP) data after cTBS, sham stimulation, and no stimulation. Visual shifts from eyes closed (EC) to eyes open (EO) and vice versa were presented via electronic goggles. Mean anteroposterior and mediolateral CoP position and oscillation, and the time delay at which body sway changed after visual shift were calculated. CoP position under both EC and EO condition was not modified after cTBS. Sway path length was greater with EC than EO and increased in both visual conditions after cTBS. CoP oscillation was also larger with EC and increased under both visual conditions after cTBS. The delay at which body oscillation changed after visual shift was longer after EC to EO than EO to EC, but unaffected by cTBS. The time constant of decrease or increase of oscillation was longer in EC to EO shifts, but unaffected by cTBS. Functional inactivation of the cerebellar vermis is associated with increased sway. Despite this, cTBS does not detectably modify onset and time course of the sensorimotor integration process of adaptation to visual shifts. Cerebellar vermis normally controls oscillation, but not timing of adaptation to abrupt changes in stabilizing information.
format Online
Article
Text
id pubmed-5243877
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-52438772017-02-01 Body Sway Increases After Functional Inactivation of the Cerebellar Vermis by cTBS Colnaghi, Silvia Honeine, Jean-Louis Sozzi, Stefania Schieppati, Marco Cerebellum Original Paper Balance stability correlates with cerebellar vermis volume. Furthermore, the cerebellum is involved in precise timing of motor processes by fine-tuning the sensorimotor integration. We tested the hypothesis that any cerebellar action in stance control and in timing of visuomotor integration for balance is impaired by continuous theta-burst stimulation (cTBS) of the vermis. Ten subjects stood quietly and underwent six sequences of 10-min acquisition of center of foot pressure (CoP) data after cTBS, sham stimulation, and no stimulation. Visual shifts from eyes closed (EC) to eyes open (EO) and vice versa were presented via electronic goggles. Mean anteroposterior and mediolateral CoP position and oscillation, and the time delay at which body sway changed after visual shift were calculated. CoP position under both EC and EO condition was not modified after cTBS. Sway path length was greater with EC than EO and increased in both visual conditions after cTBS. CoP oscillation was also larger with EC and increased under both visual conditions after cTBS. The delay at which body oscillation changed after visual shift was longer after EC to EO than EO to EC, but unaffected by cTBS. The time constant of decrease or increase of oscillation was longer in EC to EO shifts, but unaffected by cTBS. Functional inactivation of the cerebellar vermis is associated with increased sway. Despite this, cTBS does not detectably modify onset and time course of the sensorimotor integration process of adaptation to visual shifts. Cerebellar vermis normally controls oscillation, but not timing of adaptation to abrupt changes in stabilizing information. Springer US 2016-01-16 2017 /pmc/articles/PMC5243877/ /pubmed/26780373 http://dx.doi.org/10.1007/s12311-015-0758-5 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Colnaghi, Silvia
Honeine, Jean-Louis
Sozzi, Stefania
Schieppati, Marco
Body Sway Increases After Functional Inactivation of the Cerebellar Vermis by cTBS
title Body Sway Increases After Functional Inactivation of the Cerebellar Vermis by cTBS
title_full Body Sway Increases After Functional Inactivation of the Cerebellar Vermis by cTBS
title_fullStr Body Sway Increases After Functional Inactivation of the Cerebellar Vermis by cTBS
title_full_unstemmed Body Sway Increases After Functional Inactivation of the Cerebellar Vermis by cTBS
title_short Body Sway Increases After Functional Inactivation of the Cerebellar Vermis by cTBS
title_sort body sway increases after functional inactivation of the cerebellar vermis by ctbs
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243877/
https://www.ncbi.nlm.nih.gov/pubmed/26780373
http://dx.doi.org/10.1007/s12311-015-0758-5
work_keys_str_mv AT colnaghisilvia bodyswayincreasesafterfunctionalinactivationofthecerebellarvermisbyctbs
AT honeinejeanlouis bodyswayincreasesafterfunctionalinactivationofthecerebellarvermisbyctbs
AT sozzistefania bodyswayincreasesafterfunctionalinactivationofthecerebellarvermisbyctbs
AT schieppatimarco bodyswayincreasesafterfunctionalinactivationofthecerebellarvermisbyctbs