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No Gain No Pain: Relations Between Vestibulo-Ocular Reflexes and Motion Sickness in Mice
Motion sickness occurs when the vestibular system is subjected to conflicting sensory information or overstimulation. Despite the lack of knowledge about the actual underlying mechanisms, several drugs, among which scopolamine, are known to prevent or alleviate the symptoms. Here, we aim at better u...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240678/ https://www.ncbi.nlm.nih.gov/pubmed/30483206 http://dx.doi.org/10.3389/fneur.2018.00918 |
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author | Idoux, Erwin Tagliabue, Michele Beraneck, Mathieu |
author_facet | Idoux, Erwin Tagliabue, Michele Beraneck, Mathieu |
author_sort | Idoux, Erwin |
collection | PubMed |
description | Motion sickness occurs when the vestibular system is subjected to conflicting sensory information or overstimulation. Despite the lack of knowledge about the actual underlying mechanisms, several drugs, among which scopolamine, are known to prevent or alleviate the symptoms. Here, we aim at better understanding how motion sickness affects the vestibular system, as well as how scopolamine prevents motion sickness at the behavioral and cellular levels. We induced motion sickness in adult mice and tested the vestibulo-ocular responses to specific stimulations of the semi-circular canals and of the otoliths, with or without scopolamine, as well as the effects of scopolamine and muscarine on central vestibular neurons recorded on brainstem slices. We found that both motion sickness and scopolamine decrease the efficacy of the vestibulo-ocular reflexes and propose that this decrease in efficacy might be a protective mechanism to prevent later occurrences of motion sickness. To test this hypothesis, we used a behavioral paradigm based on visuo-vestibular interactions which reduces the efficacy of the vestibulo-ocular reflexes. This paradigm also offers protection against motion sickness, without requiring any drug. At the cellular level, we find that depending on the neuron, scopolamine can have opposite effects on the polarization level and firing frequency, indicating the presence of at least two types of muscarinic receptors in the medial vestibular nucleus. The present results set the basis for future studies of motion sickness counter-measures in the mouse model and offers translational perspectives for improving the treatment of affected patients. |
format | Online Article Text |
id | pubmed-6240678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62406782018-11-27 No Gain No Pain: Relations Between Vestibulo-Ocular Reflexes and Motion Sickness in Mice Idoux, Erwin Tagliabue, Michele Beraneck, Mathieu Front Neurol Neurology Motion sickness occurs when the vestibular system is subjected to conflicting sensory information or overstimulation. Despite the lack of knowledge about the actual underlying mechanisms, several drugs, among which scopolamine, are known to prevent or alleviate the symptoms. Here, we aim at better understanding how motion sickness affects the vestibular system, as well as how scopolamine prevents motion sickness at the behavioral and cellular levels. We induced motion sickness in adult mice and tested the vestibulo-ocular responses to specific stimulations of the semi-circular canals and of the otoliths, with or without scopolamine, as well as the effects of scopolamine and muscarine on central vestibular neurons recorded on brainstem slices. We found that both motion sickness and scopolamine decrease the efficacy of the vestibulo-ocular reflexes and propose that this decrease in efficacy might be a protective mechanism to prevent later occurrences of motion sickness. To test this hypothesis, we used a behavioral paradigm based on visuo-vestibular interactions which reduces the efficacy of the vestibulo-ocular reflexes. This paradigm also offers protection against motion sickness, without requiring any drug. At the cellular level, we find that depending on the neuron, scopolamine can have opposite effects on the polarization level and firing frequency, indicating the presence of at least two types of muscarinic receptors in the medial vestibular nucleus. The present results set the basis for future studies of motion sickness counter-measures in the mouse model and offers translational perspectives for improving the treatment of affected patients. Frontiers Media S.A. 2018-11-12 /pmc/articles/PMC6240678/ /pubmed/30483206 http://dx.doi.org/10.3389/fneur.2018.00918 Text en Copyright © 2018 Idoux, Tagliabue and Beraneck. http://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 | Neurology Idoux, Erwin Tagliabue, Michele Beraneck, Mathieu No Gain No Pain: Relations Between Vestibulo-Ocular Reflexes and Motion Sickness in Mice |
title | No Gain No Pain: Relations Between Vestibulo-Ocular Reflexes and Motion Sickness in Mice |
title_full | No Gain No Pain: Relations Between Vestibulo-Ocular Reflexes and Motion Sickness in Mice |
title_fullStr | No Gain No Pain: Relations Between Vestibulo-Ocular Reflexes and Motion Sickness in Mice |
title_full_unstemmed | No Gain No Pain: Relations Between Vestibulo-Ocular Reflexes and Motion Sickness in Mice |
title_short | No Gain No Pain: Relations Between Vestibulo-Ocular Reflexes and Motion Sickness in Mice |
title_sort | no gain no pain: relations between vestibulo-ocular reflexes and motion sickness in mice |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240678/ https://www.ncbi.nlm.nih.gov/pubmed/30483206 http://dx.doi.org/10.3389/fneur.2018.00918 |
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