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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...

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Autores principales: Lu, Lianyi, Cao, Ying, Tokita, Kenichi, Heck, Detlef H., Jr., John D. Boughter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
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.
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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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