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The Acute Effects of Time-Varying Caloric Vestibular Stimulation as Assessed With fMRI

We describe preliminary results from the application of time-varying caloric vestibular stimulation (tvCVS) to volunteers during a continuous blood oxygen level dependent (BOLD) functional MRI (fMRI) acquisition, recording baseline, during-tvCVS and post-tvCVS epochs. The modifications necessary to...

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Autores principales: Black, Robert D., Bell, Ryan P., Riska, Kristal M., Spankovich, Christopher, Peters, Richard W., Lascola, Christopher D., Whitlow, Christopher T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381736/
https://www.ncbi.nlm.nih.gov/pubmed/34434093
http://dx.doi.org/10.3389/fnsys.2021.648928
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author Black, Robert D.
Bell, Ryan P.
Riska, Kristal M.
Spankovich, Christopher
Peters, Richard W.
Lascola, Christopher D.
Whitlow, Christopher T.
author_facet Black, Robert D.
Bell, Ryan P.
Riska, Kristal M.
Spankovich, Christopher
Peters, Richard W.
Lascola, Christopher D.
Whitlow, Christopher T.
author_sort Black, Robert D.
collection PubMed
description We describe preliminary results from the application of time-varying caloric vestibular stimulation (tvCVS) to volunteers during a continuous blood oxygen level dependent (BOLD) functional MRI (fMRI) acquisition, recording baseline, during-tvCVS and post-tvCVS epochs. The modifications necessary to enable the use of this novel device in a 3-Tesla magnetic field are discussed. Independent component analysis (ICA) was used as a model-free method to highlight spatially and temporally coherent brain networks. The ICA results are consistent with tvCVS induction being mediated principally by thermoconvection in the vestibular labyrinth and not by direct thermal effects. The activation of hub networks identified by ICA is consistent with the concept of sensory neuromodulation, which posits that a modulatory signal introduced to a sensory organ is able to traverse the regions innervated (directly and indirectly) by that organ, while being transformed so as to be “matched” to regional neuronal dynamics. The data suggest that regional neurovascular coupling and a systemic cerebral blood flow component account for the BOLD contrast observed. The ability to modulate cerebral hemodynamics is of significant interest. The implications of these initial findings for the use of tvCVS therapeutically are discussed.
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spelling pubmed-83817362021-08-24 The Acute Effects of Time-Varying Caloric Vestibular Stimulation as Assessed With fMRI Black, Robert D. Bell, Ryan P. Riska, Kristal M. Spankovich, Christopher Peters, Richard W. Lascola, Christopher D. Whitlow, Christopher T. Front Syst Neurosci Neuroscience We describe preliminary results from the application of time-varying caloric vestibular stimulation (tvCVS) to volunteers during a continuous blood oxygen level dependent (BOLD) functional MRI (fMRI) acquisition, recording baseline, during-tvCVS and post-tvCVS epochs. The modifications necessary to enable the use of this novel device in a 3-Tesla magnetic field are discussed. Independent component analysis (ICA) was used as a model-free method to highlight spatially and temporally coherent brain networks. The ICA results are consistent with tvCVS induction being mediated principally by thermoconvection in the vestibular labyrinth and not by direct thermal effects. The activation of hub networks identified by ICA is consistent with the concept of sensory neuromodulation, which posits that a modulatory signal introduced to a sensory organ is able to traverse the regions innervated (directly and indirectly) by that organ, while being transformed so as to be “matched” to regional neuronal dynamics. The data suggest that regional neurovascular coupling and a systemic cerebral blood flow component account for the BOLD contrast observed. The ability to modulate cerebral hemodynamics is of significant interest. The implications of these initial findings for the use of tvCVS therapeutically are discussed. Frontiers Media S.A. 2021-08-09 /pmc/articles/PMC8381736/ /pubmed/34434093 http://dx.doi.org/10.3389/fnsys.2021.648928 Text en Copyright © 2021 Black, Bell, Riska, Spankovich, Peters, Lascola and Whitlow. 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
Black, Robert D.
Bell, Ryan P.
Riska, Kristal M.
Spankovich, Christopher
Peters, Richard W.
Lascola, Christopher D.
Whitlow, Christopher T.
The Acute Effects of Time-Varying Caloric Vestibular Stimulation as Assessed With fMRI
title The Acute Effects of Time-Varying Caloric Vestibular Stimulation as Assessed With fMRI
title_full The Acute Effects of Time-Varying Caloric Vestibular Stimulation as Assessed With fMRI
title_fullStr The Acute Effects of Time-Varying Caloric Vestibular Stimulation as Assessed With fMRI
title_full_unstemmed The Acute Effects of Time-Varying Caloric Vestibular Stimulation as Assessed With fMRI
title_short The Acute Effects of Time-Varying Caloric Vestibular Stimulation as Assessed With fMRI
title_sort acute effects of time-varying caloric vestibular stimulation as assessed with fmri
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381736/
https://www.ncbi.nlm.nih.gov/pubmed/34434093
http://dx.doi.org/10.3389/fnsys.2021.648928
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