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Positron emission tomography visualized stimulation of the vestibular organ is localized in Heschl's gyrus

The existence of a human primary vestibular cortex is still debated. Current knowledge mainly derives from functional magnetic resonance imaging (fMRI) and positron emission tomography (PET) acquisitions during artificial vestibular stimulation. This may be problematic as artificial vestibular stimu...

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Autores principales: Devantier, Louise, Hansen, Allan K., Mølby‐Henriksen, Jens‐Jacob, Christensen, Christian B., Pedersen, Michael, Hansen, Kim V., Magnusson, Måns, Ovesen, Therese, Borghammer, Per
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268041/
https://www.ncbi.nlm.nih.gov/pubmed/31520516
http://dx.doi.org/10.1002/hbm.24798
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author Devantier, Louise
Hansen, Allan K.
Mølby‐Henriksen, Jens‐Jacob
Christensen, Christian B.
Pedersen, Michael
Hansen, Kim V.
Magnusson, Måns
Ovesen, Therese
Borghammer, Per
author_facet Devantier, Louise
Hansen, Allan K.
Mølby‐Henriksen, Jens‐Jacob
Christensen, Christian B.
Pedersen, Michael
Hansen, Kim V.
Magnusson, Måns
Ovesen, Therese
Borghammer, Per
author_sort Devantier, Louise
collection PubMed
description The existence of a human primary vestibular cortex is still debated. Current knowledge mainly derives from functional magnetic resonance imaging (fMRI) and positron emission tomography (PET) acquisitions during artificial vestibular stimulation. This may be problematic as artificial vestibular stimulation entails coactivation of other sensory receptors. The use of fMRI is challenging as the strong magnetic field and loud noise during MRI may both stimulate the vestibular organ. This study aimed to characterize the cortical activity during natural stimulation of the human vestibular organ. Two fluorodeoxyglucose (FDG)‐PET scans were obtained after natural vestibular stimulation in a self‐propelled chair. Two types of stimuli were applied: (a) rotation (horizontal semicircular canal) and (b) linear sideways movement (utriculus). A comparable baseline FDG‐PET scan was obtained after sitting motion‐less in the chair. In both stimulation paradigms, significantly increased FDG uptake was measured bilaterally in the medial part of Heschl's gyrus, with some overlap into the posterior insula. This is the first neuroimaging study to visualize cortical processing of natural vestibular stimuli. FDG uptake was demonstrated in the medial‐most part of Heschl's gyrus, normally associated with the primary auditory cortex. This anatomical localization seems plausible, considering that the labyrinth contains both the vestibular organ and the cochlea.
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spelling pubmed-72680412020-06-12 Positron emission tomography visualized stimulation of the vestibular organ is localized in Heschl's gyrus Devantier, Louise Hansen, Allan K. Mølby‐Henriksen, Jens‐Jacob Christensen, Christian B. Pedersen, Michael Hansen, Kim V. Magnusson, Måns Ovesen, Therese Borghammer, Per Hum Brain Mapp Research Articles The existence of a human primary vestibular cortex is still debated. Current knowledge mainly derives from functional magnetic resonance imaging (fMRI) and positron emission tomography (PET) acquisitions during artificial vestibular stimulation. This may be problematic as artificial vestibular stimulation entails coactivation of other sensory receptors. The use of fMRI is challenging as the strong magnetic field and loud noise during MRI may both stimulate the vestibular organ. This study aimed to characterize the cortical activity during natural stimulation of the human vestibular organ. Two fluorodeoxyglucose (FDG)‐PET scans were obtained after natural vestibular stimulation in a self‐propelled chair. Two types of stimuli were applied: (a) rotation (horizontal semicircular canal) and (b) linear sideways movement (utriculus). A comparable baseline FDG‐PET scan was obtained after sitting motion‐less in the chair. In both stimulation paradigms, significantly increased FDG uptake was measured bilaterally in the medial part of Heschl's gyrus, with some overlap into the posterior insula. This is the first neuroimaging study to visualize cortical processing of natural vestibular stimuli. FDG uptake was demonstrated in the medial‐most part of Heschl's gyrus, normally associated with the primary auditory cortex. This anatomical localization seems plausible, considering that the labyrinth contains both the vestibular organ and the cochlea. John Wiley & Sons, Inc. 2019-09-14 /pmc/articles/PMC7268041/ /pubmed/31520516 http://dx.doi.org/10.1002/hbm.24798 Text en © 2019 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Devantier, Louise
Hansen, Allan K.
Mølby‐Henriksen, Jens‐Jacob
Christensen, Christian B.
Pedersen, Michael
Hansen, Kim V.
Magnusson, Måns
Ovesen, Therese
Borghammer, Per
Positron emission tomography visualized stimulation of the vestibular organ is localized in Heschl's gyrus
title Positron emission tomography visualized stimulation of the vestibular organ is localized in Heschl's gyrus
title_full Positron emission tomography visualized stimulation of the vestibular organ is localized in Heschl's gyrus
title_fullStr Positron emission tomography visualized stimulation of the vestibular organ is localized in Heschl's gyrus
title_full_unstemmed Positron emission tomography visualized stimulation of the vestibular organ is localized in Heschl's gyrus
title_short Positron emission tomography visualized stimulation of the vestibular organ is localized in Heschl's gyrus
title_sort positron emission tomography visualized stimulation of the vestibular organ is localized in heschl's gyrus
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268041/
https://www.ncbi.nlm.nih.gov/pubmed/31520516
http://dx.doi.org/10.1002/hbm.24798
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