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Neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate

Galvanic vestibular stimulation (GVS) uses the external application of electrical current to selectively target the vestibular system in humans. Despite its recent popularity for the assessment/treatment of clinical conditions, exactly how this non-invasive tool activates the vestibular system remai...

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Autores principales: Kwan, Annie, Forbes, Patrick A., Mitchell, Diana E., Blouin, Jean-Sébastien, Cullen, Kathleen E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478681/
https://www.ncbi.nlm.nih.gov/pubmed/31015434
http://dx.doi.org/10.1038/s41467-019-09738-1
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author Kwan, Annie
Forbes, Patrick A.
Mitchell, Diana E.
Blouin, Jean-Sébastien
Cullen, Kathleen E.
author_facet Kwan, Annie
Forbes, Patrick A.
Mitchell, Diana E.
Blouin, Jean-Sébastien
Cullen, Kathleen E.
author_sort Kwan, Annie
collection PubMed
description Galvanic vestibular stimulation (GVS) uses the external application of electrical current to selectively target the vestibular system in humans. Despite its recent popularity for the assessment/treatment of clinical conditions, exactly how this non-invasive tool activates the vestibular system remains an open question. Here we directly investigate single vestibular afferent responses to GVS applied to the mastoid processes of awake-behaving monkeys. Transmastoid GVS produces robust and parallel activation of both canal and otolith afferents. Notably, afferent activation increases with intrinsic neuronal variability resulting in constant GVS-evoked neuronal detection thresholds across all afferents. Additionally, afferent tuning differs for GVS versus natural self-motion stimulation. Using a stochastic model of repetitive activity in afferents, we largely explain the main features of GVS-evoked vestibular afferent dynamics. Taken together, our results reveal the neural substrate underlying transmastoid GVS-evoked perceptual, ocular and postural responses—information that is essential to advance GVS applicability for biomedical uses in humans.
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spelling pubmed-64786812019-04-25 Neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate Kwan, Annie Forbes, Patrick A. Mitchell, Diana E. Blouin, Jean-Sébastien Cullen, Kathleen E. Nat Commun Article Galvanic vestibular stimulation (GVS) uses the external application of electrical current to selectively target the vestibular system in humans. Despite its recent popularity for the assessment/treatment of clinical conditions, exactly how this non-invasive tool activates the vestibular system remains an open question. Here we directly investigate single vestibular afferent responses to GVS applied to the mastoid processes of awake-behaving monkeys. Transmastoid GVS produces robust and parallel activation of both canal and otolith afferents. Notably, afferent activation increases with intrinsic neuronal variability resulting in constant GVS-evoked neuronal detection thresholds across all afferents. Additionally, afferent tuning differs for GVS versus natural self-motion stimulation. Using a stochastic model of repetitive activity in afferents, we largely explain the main features of GVS-evoked vestibular afferent dynamics. Taken together, our results reveal the neural substrate underlying transmastoid GVS-evoked perceptual, ocular and postural responses—information that is essential to advance GVS applicability for biomedical uses in humans. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478681/ /pubmed/31015434 http://dx.doi.org/10.1038/s41467-019-09738-1 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kwan, Annie
Forbes, Patrick A.
Mitchell, Diana E.
Blouin, Jean-Sébastien
Cullen, Kathleen E.
Neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate
title Neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate
title_full Neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate
title_fullStr Neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate
title_full_unstemmed Neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate
title_short Neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate
title_sort neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478681/
https://www.ncbi.nlm.nih.gov/pubmed/31015434
http://dx.doi.org/10.1038/s41467-019-09738-1
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