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The mammalian efferent vestibular system utilizes cholinergic mechanisms to excite primary vestibular afferents

Electrical stimulation of the mammalian efferent vestibular system (EVS) predominantly excites primary vestibular afferents along two distinct time scales. Although roles for acetylcholine (ACh) have been demonstrated in other vertebrates, synaptic mechanisms underlying mammalian EVS actions are not...

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Autores principales: Schneider, Glenn T., Lee, Choongheon, Sinha, Anjali K., Jordan, Paivi M., Holt, Joseph C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806594/
https://www.ncbi.nlm.nih.gov/pubmed/33441862
http://dx.doi.org/10.1038/s41598-020-80367-1
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author Schneider, Glenn T.
Lee, Choongheon
Sinha, Anjali K.
Jordan, Paivi M.
Holt, Joseph C.
author_facet Schneider, Glenn T.
Lee, Choongheon
Sinha, Anjali K.
Jordan, Paivi M.
Holt, Joseph C.
author_sort Schneider, Glenn T.
collection PubMed
description Electrical stimulation of the mammalian efferent vestibular system (EVS) predominantly excites primary vestibular afferents along two distinct time scales. Although roles for acetylcholine (ACh) have been demonstrated in other vertebrates, synaptic mechanisms underlying mammalian EVS actions are not well-characterized. To determine if activation of ACh receptors account for efferent-mediated afferent excitation in mammals, we recorded afferent activity from the superior vestibular nerve of anesthetized C57BL/6 mice while stimulating EVS neurons in the brainstem, before and after administration of cholinergic antagonists. Using a normalized coefficient of variation (CV*), we broadly classified vestibular afferents as regularly- (CV* < 0.1) or irregularly-discharging (CV* > 0.1) and characterized their responses to midline or ipsilateral EVS stimulation. Afferent responses to efferent stimulation were predominantly excitatory, grew in amplitude with increasing CV*, and consisted of fast and slow components that could be identified by differences in rise time and post-stimulus duration. Both efferent-mediated excitatory components were larger in irregular afferents with ipsilateral EVS stimulation. Our pharmacological data show, for the first time in mammals, that muscarinic AChR antagonists block efferent-mediated slow excitation whereas the nicotinic AChR antagonist DHβE selectively blocks efferent-mediated fast excitation, while leaving the efferent-mediated slow component intact. These data confirm that mammalian EVS actions are predominantly cholinergic.
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spelling pubmed-78065942021-01-14 The mammalian efferent vestibular system utilizes cholinergic mechanisms to excite primary vestibular afferents Schneider, Glenn T. Lee, Choongheon Sinha, Anjali K. Jordan, Paivi M. Holt, Joseph C. Sci Rep Article Electrical stimulation of the mammalian efferent vestibular system (EVS) predominantly excites primary vestibular afferents along two distinct time scales. Although roles for acetylcholine (ACh) have been demonstrated in other vertebrates, synaptic mechanisms underlying mammalian EVS actions are not well-characterized. To determine if activation of ACh receptors account for efferent-mediated afferent excitation in mammals, we recorded afferent activity from the superior vestibular nerve of anesthetized C57BL/6 mice while stimulating EVS neurons in the brainstem, before and after administration of cholinergic antagonists. Using a normalized coefficient of variation (CV*), we broadly classified vestibular afferents as regularly- (CV* < 0.1) or irregularly-discharging (CV* > 0.1) and characterized their responses to midline or ipsilateral EVS stimulation. Afferent responses to efferent stimulation were predominantly excitatory, grew in amplitude with increasing CV*, and consisted of fast and slow components that could be identified by differences in rise time and post-stimulus duration. Both efferent-mediated excitatory components were larger in irregular afferents with ipsilateral EVS stimulation. Our pharmacological data show, for the first time in mammals, that muscarinic AChR antagonists block efferent-mediated slow excitation whereas the nicotinic AChR antagonist DHβE selectively blocks efferent-mediated fast excitation, while leaving the efferent-mediated slow component intact. These data confirm that mammalian EVS actions are predominantly cholinergic. Nature Publishing Group UK 2021-01-13 /pmc/articles/PMC7806594/ /pubmed/33441862 http://dx.doi.org/10.1038/s41598-020-80367-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Schneider, Glenn T.
Lee, Choongheon
Sinha, Anjali K.
Jordan, Paivi M.
Holt, Joseph C.
The mammalian efferent vestibular system utilizes cholinergic mechanisms to excite primary vestibular afferents
title The mammalian efferent vestibular system utilizes cholinergic mechanisms to excite primary vestibular afferents
title_full The mammalian efferent vestibular system utilizes cholinergic mechanisms to excite primary vestibular afferents
title_fullStr The mammalian efferent vestibular system utilizes cholinergic mechanisms to excite primary vestibular afferents
title_full_unstemmed The mammalian efferent vestibular system utilizes cholinergic mechanisms to excite primary vestibular afferents
title_short The mammalian efferent vestibular system utilizes cholinergic mechanisms to excite primary vestibular afferents
title_sort mammalian efferent vestibular system utilizes cholinergic mechanisms to excite primary vestibular afferents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806594/
https://www.ncbi.nlm.nih.gov/pubmed/33441862
http://dx.doi.org/10.1038/s41598-020-80367-1
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