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Absence of Nonlinear Coupling Between Electric Vestibular Stimulation and Evoked Forces During Standing Balance
The vestibular system encodes motion and orientation of the head in space and is essential for negotiating in and interacting with the world. Recently, random waveform electric vestibular stimulation has become an increasingly common means of probing the vestibular system. However, many of the metho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046432/ https://www.ncbi.nlm.nih.gov/pubmed/33867958 http://dx.doi.org/10.3389/fnhum.2021.631782 |
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author | Hannan, Kelci B. Todd, Makina K. Pearson, Nicole J. Forbes, Patrick A. Dakin, Christopher J. |
author_facet | Hannan, Kelci B. Todd, Makina K. Pearson, Nicole J. Forbes, Patrick A. Dakin, Christopher J. |
author_sort | Hannan, Kelci B. |
collection | PubMed |
description | The vestibular system encodes motion and orientation of the head in space and is essential for negotiating in and interacting with the world. Recently, random waveform electric vestibular stimulation has become an increasingly common means of probing the vestibular system. However, many of the methods used to analyze the behavioral response to this type of stimulation assume a linear relationship between frequencies in the stimulus and its associated response. Here we examine this stimulus-response frequency linearity to determine the validity of this assumption. Forty-five university-aged subjects stood on a force-plate for 4 min while receiving vestibular stimulation. To determine the linearity of the stimulus-response relationship we calculated the cross-frequency power coupling between a 0 and 25 Hz bandwidth limited white noise stimulus and induced postural responses, as measured using the horizontal forces acting at the feet. Ultimately, we found that, on average, the postural response to a random stimulus is linear across stimulation frequencies. This result supports the use of analysis methods that depend on the assumption of stimulus-response frequency linearity, such as coherence and gain, which are commonly used to analyze the body’s response to random waveform electric stimuli. |
format | Online Article Text |
id | pubmed-8046432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80464322021-04-15 Absence of Nonlinear Coupling Between Electric Vestibular Stimulation and Evoked Forces During Standing Balance Hannan, Kelci B. Todd, Makina K. Pearson, Nicole J. Forbes, Patrick A. Dakin, Christopher J. Front Hum Neurosci Neuroscience The vestibular system encodes motion and orientation of the head in space and is essential for negotiating in and interacting with the world. Recently, random waveform electric vestibular stimulation has become an increasingly common means of probing the vestibular system. However, many of the methods used to analyze the behavioral response to this type of stimulation assume a linear relationship between frequencies in the stimulus and its associated response. Here we examine this stimulus-response frequency linearity to determine the validity of this assumption. Forty-five university-aged subjects stood on a force-plate for 4 min while receiving vestibular stimulation. To determine the linearity of the stimulus-response relationship we calculated the cross-frequency power coupling between a 0 and 25 Hz bandwidth limited white noise stimulus and induced postural responses, as measured using the horizontal forces acting at the feet. Ultimately, we found that, on average, the postural response to a random stimulus is linear across stimulation frequencies. This result supports the use of analysis methods that depend on the assumption of stimulus-response frequency linearity, such as coherence and gain, which are commonly used to analyze the body’s response to random waveform electric stimuli. Frontiers Media S.A. 2021-03-25 /pmc/articles/PMC8046432/ /pubmed/33867958 http://dx.doi.org/10.3389/fnhum.2021.631782 Text en Copyright © 2021 Hannan, Todd, Pearson, Forbes and Dakin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Hannan, Kelci B. Todd, Makina K. Pearson, Nicole J. Forbes, Patrick A. Dakin, Christopher J. Absence of Nonlinear Coupling Between Electric Vestibular Stimulation and Evoked Forces During Standing Balance |
title | Absence of Nonlinear Coupling Between Electric Vestibular Stimulation and Evoked Forces During Standing Balance |
title_full | Absence of Nonlinear Coupling Between Electric Vestibular Stimulation and Evoked Forces During Standing Balance |
title_fullStr | Absence of Nonlinear Coupling Between Electric Vestibular Stimulation and Evoked Forces During Standing Balance |
title_full_unstemmed | Absence of Nonlinear Coupling Between Electric Vestibular Stimulation and Evoked Forces During Standing Balance |
title_short | Absence of Nonlinear Coupling Between Electric Vestibular Stimulation and Evoked Forces During Standing Balance |
title_sort | absence of nonlinear coupling between electric vestibular stimulation and evoked forces during standing balance |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046432/ https://www.ncbi.nlm.nih.gov/pubmed/33867958 http://dx.doi.org/10.3389/fnhum.2021.631782 |
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