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Noisy Galvanic Vestibular Stimulation Modulates the Amplitude of EEG Synchrony Patterns
Noisy galvanic vestibular stimulation has been associated with numerous cognitive and behavioural effects, such as enhancement of visual memory in healthy individuals, improvement of visual deficits in stroke patients, as well as possibly improvement of motor function in Parkinson’s disease; yet, th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715484/ https://www.ncbi.nlm.nih.gov/pubmed/23874865 http://dx.doi.org/10.1371/journal.pone.0069055 |
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author | Kim, Diana J. Yogendrakumar, Vignan Chiang, Joyce Ty, Edna Wang, Z. Jane McKeown, Martin J. |
author_facet | Kim, Diana J. Yogendrakumar, Vignan Chiang, Joyce Ty, Edna Wang, Z. Jane McKeown, Martin J. |
author_sort | Kim, Diana J. |
collection | PubMed |
description | Noisy galvanic vestibular stimulation has been associated with numerous cognitive and behavioural effects, such as enhancement of visual memory in healthy individuals, improvement of visual deficits in stroke patients, as well as possibly improvement of motor function in Parkinson’s disease; yet, the mechanism of action is unclear. Since Parkinson’s and other neuropsychiatric diseases are characterized by maladaptive dynamics of brain rhythms, we investigated whether noisy galvanic vestibular stimulation was associated with measurable changes in EEG oscillatory rhythms within theta (4–7.5 Hz), low alpha (8–10 Hz), high alpha (10.5–12 Hz), beta (13–30 Hz) and gamma (31–50 Hz) bands. We recorded the EEG while simultaneously delivering noisy bilateral, bipolar stimulation at varying intensities of imperceptible currents – at 10, 26, 42, 58, 74 and 90% of sensory threshold – to ten neurologically healthy subjects. Using standard spectral analysis, we investigated the transient aftereffects of noisy stimulation on rhythms. Subsequently, using robust artifact rejection techniques and the Least Absolute Shrinkage Selection Operator regression and cross-validation, we assessed the combinations of channels and power spectral features within each EEG frequency band that were linearly related with stimulus intensity. We show that noisy galvanic vestibular stimulation predominantly leads to a mild suppression of gamma power in lateral regions immediately after stimulation, followed by delayed increase in beta and gamma power in frontal regions approximately 20–25 s after stimulation ceased. Ongoing changes in the power of each oscillatory band throughout frontal, central/parietal, occipital and bilateral electrodes predicted the intensity of galvanic vestibular stimulation in a stimulus-dependent manner, demonstrating linear effects of stimulation on brain rhythms. We propose that modulation of neural oscillations is a potential mechanism for the previously-described cognitive and motor effects of vestibular stimulation, and noisy galvanic vestibular stimulation may provide an additional non-invasive means for neuromodulation of functional brain networks. |
format | Online Article Text |
id | pubmed-3715484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37154842013-07-19 Noisy Galvanic Vestibular Stimulation Modulates the Amplitude of EEG Synchrony Patterns Kim, Diana J. Yogendrakumar, Vignan Chiang, Joyce Ty, Edna Wang, Z. Jane McKeown, Martin J. PLoS One Research Article Noisy galvanic vestibular stimulation has been associated with numerous cognitive and behavioural effects, such as enhancement of visual memory in healthy individuals, improvement of visual deficits in stroke patients, as well as possibly improvement of motor function in Parkinson’s disease; yet, the mechanism of action is unclear. Since Parkinson’s and other neuropsychiatric diseases are characterized by maladaptive dynamics of brain rhythms, we investigated whether noisy galvanic vestibular stimulation was associated with measurable changes in EEG oscillatory rhythms within theta (4–7.5 Hz), low alpha (8–10 Hz), high alpha (10.5–12 Hz), beta (13–30 Hz) and gamma (31–50 Hz) bands. We recorded the EEG while simultaneously delivering noisy bilateral, bipolar stimulation at varying intensities of imperceptible currents – at 10, 26, 42, 58, 74 and 90% of sensory threshold – to ten neurologically healthy subjects. Using standard spectral analysis, we investigated the transient aftereffects of noisy stimulation on rhythms. Subsequently, using robust artifact rejection techniques and the Least Absolute Shrinkage Selection Operator regression and cross-validation, we assessed the combinations of channels and power spectral features within each EEG frequency band that were linearly related with stimulus intensity. We show that noisy galvanic vestibular stimulation predominantly leads to a mild suppression of gamma power in lateral regions immediately after stimulation, followed by delayed increase in beta and gamma power in frontal regions approximately 20–25 s after stimulation ceased. Ongoing changes in the power of each oscillatory band throughout frontal, central/parietal, occipital and bilateral electrodes predicted the intensity of galvanic vestibular stimulation in a stimulus-dependent manner, demonstrating linear effects of stimulation on brain rhythms. We propose that modulation of neural oscillations is a potential mechanism for the previously-described cognitive and motor effects of vestibular stimulation, and noisy galvanic vestibular stimulation may provide an additional non-invasive means for neuromodulation of functional brain networks. Public Library of Science 2013-07-18 /pmc/articles/PMC3715484/ /pubmed/23874865 http://dx.doi.org/10.1371/journal.pone.0069055 Text en © 2013 Kim et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kim, Diana J. Yogendrakumar, Vignan Chiang, Joyce Ty, Edna Wang, Z. Jane McKeown, Martin J. Noisy Galvanic Vestibular Stimulation Modulates the Amplitude of EEG Synchrony Patterns |
title | Noisy Galvanic Vestibular Stimulation Modulates the Amplitude of EEG Synchrony Patterns |
title_full | Noisy Galvanic Vestibular Stimulation Modulates the Amplitude of EEG Synchrony Patterns |
title_fullStr | Noisy Galvanic Vestibular Stimulation Modulates the Amplitude of EEG Synchrony Patterns |
title_full_unstemmed | Noisy Galvanic Vestibular Stimulation Modulates the Amplitude of EEG Synchrony Patterns |
title_short | Noisy Galvanic Vestibular Stimulation Modulates the Amplitude of EEG Synchrony Patterns |
title_sort | noisy galvanic vestibular stimulation modulates the amplitude of eeg synchrony patterns |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715484/ https://www.ncbi.nlm.nih.gov/pubmed/23874865 http://dx.doi.org/10.1371/journal.pone.0069055 |
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