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Medial cerebellar nuclear projections and activity patterns link cerebellar output to orofacial and respiratory behavior
There is ample evidence that the cerebellum plays an important role in coordinating both respiratory and orofacial movements. However, the pathway by which the cerebellum engages brainstem substrates underlying these movements is not well understood. We used tract-tracing techniques in mice to show...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613706/ https://www.ncbi.nlm.nih.gov/pubmed/23565078 http://dx.doi.org/10.3389/fncir.2013.00056 |
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author | Lu, Lianyi Cao, Ying Tokita, Kenichi Heck, Detlef H. Jr., John D. Boughter |
author_facet | Lu, Lianyi Cao, Ying Tokita, Kenichi Heck, Detlef H. Jr., John D. Boughter |
author_sort | Lu, Lianyi |
collection | PubMed |
description | There is ample evidence that the cerebellum plays an important role in coordinating both respiratory and orofacial movements. However, the pathway by which the cerebellum engages brainstem substrates underlying these movements is not well understood. We used tract-tracing techniques in mice to show that neurons in the medial deep cerebellar nucleus (mDCN) project directly to these putative substrates. Injection of an anterograde tracer into the mDCN produced terminal labeling in the ventromedial medullary reticular formation, which was stronger on the contralateral side. Correspondingly, injection of retrograde tracers into these same areas resulted in robust neuronal cell labeling in the contralateral mDCN. Moreover, injection of two retrograde tracers at different rostral–caudal brainstem levels resulted in a subset of double-labeled cells, indicating that single mDCN neurons collateralize to multiple substrates. Using an awake and behaving recording preparation, we show that spiking activity in mDCN neurons is correlated with respiratory and orofacial behaviors, including whisking and fluid licking. Almost half of the recorded neurons showed activity correlated with more than one behavior, suggesting that these neurons may in fact modulate multiple brainstem substrates. Collectively, these results describe a potential pathway through which the cerebellum could modulate and coordinate respiratory and orofacial behaviors. |
format | Online Article Text |
id | pubmed-3613706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36137062013-04-05 Medial cerebellar nuclear projections and activity patterns link cerebellar output to orofacial and respiratory behavior Lu, Lianyi Cao, Ying Tokita, Kenichi Heck, Detlef H. Jr., John D. Boughter Front Neural Circuits Neuroscience There is ample evidence that the cerebellum plays an important role in coordinating both respiratory and orofacial movements. However, the pathway by which the cerebellum engages brainstem substrates underlying these movements is not well understood. We used tract-tracing techniques in mice to show that neurons in the medial deep cerebellar nucleus (mDCN) project directly to these putative substrates. Injection of an anterograde tracer into the mDCN produced terminal labeling in the ventromedial medullary reticular formation, which was stronger on the contralateral side. Correspondingly, injection of retrograde tracers into these same areas resulted in robust neuronal cell labeling in the contralateral mDCN. Moreover, injection of two retrograde tracers at different rostral–caudal brainstem levels resulted in a subset of double-labeled cells, indicating that single mDCN neurons collateralize to multiple substrates. Using an awake and behaving recording preparation, we show that spiking activity in mDCN neurons is correlated with respiratory and orofacial behaviors, including whisking and fluid licking. Almost half of the recorded neurons showed activity correlated with more than one behavior, suggesting that these neurons may in fact modulate multiple brainstem substrates. Collectively, these results describe a potential pathway through which the cerebellum could modulate and coordinate respiratory and orofacial behaviors. Frontiers Media S.A. 2013-04-02 /pmc/articles/PMC3613706/ /pubmed/23565078 http://dx.doi.org/10.3389/fncir.2013.00056 Text en Copyright © Lu, Cao, Tokita, Heck and Boughter. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Neuroscience Lu, Lianyi Cao, Ying Tokita, Kenichi Heck, Detlef H. Jr., John D. Boughter Medial cerebellar nuclear projections and activity patterns link cerebellar output to orofacial and respiratory behavior |
title | Medial cerebellar nuclear projections and activity patterns link cerebellar output to orofacial and respiratory behavior |
title_full | Medial cerebellar nuclear projections and activity patterns link cerebellar output to orofacial and respiratory behavior |
title_fullStr | Medial cerebellar nuclear projections and activity patterns link cerebellar output to orofacial and respiratory behavior |
title_full_unstemmed | Medial cerebellar nuclear projections and activity patterns link cerebellar output to orofacial and respiratory behavior |
title_short | Medial cerebellar nuclear projections and activity patterns link cerebellar output to orofacial and respiratory behavior |
title_sort | medial cerebellar nuclear projections and activity patterns link cerebellar output to orofacial and respiratory behavior |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613706/ https://www.ncbi.nlm.nih.gov/pubmed/23565078 http://dx.doi.org/10.3389/fncir.2013.00056 |
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