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Vestibular Activation Differentially Modulates Human Early Visual Cortex and V5/MT Excitability and Response Entropy

Head movement imposes the additional burdens on the visual system of maintaining visual acuity and determining the origin of retinal image motion (i.e., self-motion vs. object-motion). Although maintaining visual acuity during self-motion is effected by minimizing retinal slip via the brainstem vest...

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Autores principales: Seemungal, Barry M, Guzman-Lopez, Jessica, Arshad, Qadeer, Schultz, Simon R, Walsh, Vincent, Yousif, Nada
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3513948/
https://www.ncbi.nlm.nih.gov/pubmed/22291031
http://dx.doi.org/10.1093/cercor/bhr366
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author Seemungal, Barry M
Guzman-Lopez, Jessica
Arshad, Qadeer
Schultz, Simon R
Walsh, Vincent
Yousif, Nada
author_facet Seemungal, Barry M
Guzman-Lopez, Jessica
Arshad, Qadeer
Schultz, Simon R
Walsh, Vincent
Yousif, Nada
author_sort Seemungal, Barry M
collection PubMed
description Head movement imposes the additional burdens on the visual system of maintaining visual acuity and determining the origin of retinal image motion (i.e., self-motion vs. object-motion). Although maintaining visual acuity during self-motion is effected by minimizing retinal slip via the brainstem vestibular-ocular reflex, higher order visuovestibular mechanisms also contribute. Disambiguating self-motion versus object-motion also invokes higher order mechanisms, and a cortical visuovestibular reciprocal antagonism is propounded. Hence, one prediction is of a vestibular modulation of visual cortical excitability and indirect measures have variously suggested none, focal or global effects of activation or suppression in human visual cortex. Using transcranial magnetic stimulation-induced phosphenes to probe cortical excitability, we observed decreased V5/MT excitability versus increased early visual cortex (EVC) excitability, during vestibular activation. In order to exclude nonspecific effects (e.g., arousal) on cortical excitability, response specificity was assessed using information theory, specifically response entropy. Vestibular activation significantly modulated phosphene response entropy for V5/MT but not EVC, implying a specific vestibular effect on V5/MT responses. This is the first demonstration that vestibular activation modulates human visual cortex excitability. Furthermore, using information theory, not previously used in phosphene response analysis, we could distinguish between a specific vestibular modulation of V5/MT excitability from a nonspecific effect at EVC.
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spelling pubmed-35139482012-12-04 Vestibular Activation Differentially Modulates Human Early Visual Cortex and V5/MT Excitability and Response Entropy Seemungal, Barry M Guzman-Lopez, Jessica Arshad, Qadeer Schultz, Simon R Walsh, Vincent Yousif, Nada Cereb Cortex Articles Head movement imposes the additional burdens on the visual system of maintaining visual acuity and determining the origin of retinal image motion (i.e., self-motion vs. object-motion). Although maintaining visual acuity during self-motion is effected by minimizing retinal slip via the brainstem vestibular-ocular reflex, higher order visuovestibular mechanisms also contribute. Disambiguating self-motion versus object-motion also invokes higher order mechanisms, and a cortical visuovestibular reciprocal antagonism is propounded. Hence, one prediction is of a vestibular modulation of visual cortical excitability and indirect measures have variously suggested none, focal or global effects of activation or suppression in human visual cortex. Using transcranial magnetic stimulation-induced phosphenes to probe cortical excitability, we observed decreased V5/MT excitability versus increased early visual cortex (EVC) excitability, during vestibular activation. In order to exclude nonspecific effects (e.g., arousal) on cortical excitability, response specificity was assessed using information theory, specifically response entropy. Vestibular activation significantly modulated phosphene response entropy for V5/MT but not EVC, implying a specific vestibular effect on V5/MT responses. This is the first demonstration that vestibular activation modulates human visual cortex excitability. Furthermore, using information theory, not previously used in phosphene response analysis, we could distinguish between a specific vestibular modulation of V5/MT excitability from a nonspecific effect at EVC. Oxford University Press 2013-01 2012-01-30 /pmc/articles/PMC3513948/ /pubmed/22291031 http://dx.doi.org/10.1093/cercor/bhr366 Text en © The Authors 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Seemungal, Barry M
Guzman-Lopez, Jessica
Arshad, Qadeer
Schultz, Simon R
Walsh, Vincent
Yousif, Nada
Vestibular Activation Differentially Modulates Human Early Visual Cortex and V5/MT Excitability and Response Entropy
title Vestibular Activation Differentially Modulates Human Early Visual Cortex and V5/MT Excitability and Response Entropy
title_full Vestibular Activation Differentially Modulates Human Early Visual Cortex and V5/MT Excitability and Response Entropy
title_fullStr Vestibular Activation Differentially Modulates Human Early Visual Cortex and V5/MT Excitability and Response Entropy
title_full_unstemmed Vestibular Activation Differentially Modulates Human Early Visual Cortex and V5/MT Excitability and Response Entropy
title_short Vestibular Activation Differentially Modulates Human Early Visual Cortex and V5/MT Excitability and Response Entropy
title_sort vestibular activation differentially modulates human early visual cortex and v5/mt excitability and response entropy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3513948/
https://www.ncbi.nlm.nih.gov/pubmed/22291031
http://dx.doi.org/10.1093/cercor/bhr366
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