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Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus
Navigation requires not only the execution of locomotor programs but also high arousal and real-time retrieval of spatial memory that is often associated with hippocampal theta oscillations. However, the neural circuits for coordinately controlling these important processes remain to be fully dissec...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959274/ https://www.ncbi.nlm.nih.gov/pubmed/31937768 http://dx.doi.org/10.1038/s41467-019-14116-y |
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author | Lu, Lihui Ren, Yuqi Yu, Tao Liu, Zhixiang Wang, Sice Tan, Lubin Zeng, Jiawei Feng, Qiru Lin, Rui Liu, Yang Guo, Qingchun Luo, Minmin |
author_facet | Lu, Lihui Ren, Yuqi Yu, Tao Liu, Zhixiang Wang, Sice Tan, Lubin Zeng, Jiawei Feng, Qiru Lin, Rui Liu, Yang Guo, Qingchun Luo, Minmin |
author_sort | Lu, Lihui |
collection | PubMed |
description | Navigation requires not only the execution of locomotor programs but also high arousal and real-time retrieval of spatial memory that is often associated with hippocampal theta oscillations. However, the neural circuits for coordinately controlling these important processes remain to be fully dissected. Here we show that the activity of the neuromedin B (NMB) neurons in the nucleus incertus (NI) is tightly correlated with mouse locomotor speed, arousal level, and hippocampal theta power. These processes are reversibly suppressed by optogenetic inhibition and rapidly promoted by optogenetic stimulation of NI NMB neurons. These neurons form reciprocal connections with several subcortical areas associated with arousal, theta oscillation, and premotor processing. Their projections to multiple downstream stations regulate locomotion and hippocampal theta, with the projection to the medial septum being particularly important for promoting arousal. Therefore, NI NMB neurons functionally impact the neural circuit for navigation control according to particular brains states. |
format | Online Article Text |
id | pubmed-6959274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69592742020-01-15 Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus Lu, Lihui Ren, Yuqi Yu, Tao Liu, Zhixiang Wang, Sice Tan, Lubin Zeng, Jiawei Feng, Qiru Lin, Rui Liu, Yang Guo, Qingchun Luo, Minmin Nat Commun Article Navigation requires not only the execution of locomotor programs but also high arousal and real-time retrieval of spatial memory that is often associated with hippocampal theta oscillations. However, the neural circuits for coordinately controlling these important processes remain to be fully dissected. Here we show that the activity of the neuromedin B (NMB) neurons in the nucleus incertus (NI) is tightly correlated with mouse locomotor speed, arousal level, and hippocampal theta power. These processes are reversibly suppressed by optogenetic inhibition and rapidly promoted by optogenetic stimulation of NI NMB neurons. These neurons form reciprocal connections with several subcortical areas associated with arousal, theta oscillation, and premotor processing. Their projections to multiple downstream stations regulate locomotion and hippocampal theta, with the projection to the medial septum being particularly important for promoting arousal. Therefore, NI NMB neurons functionally impact the neural circuit for navigation control according to particular brains states. Nature Publishing Group UK 2020-01-14 /pmc/articles/PMC6959274/ /pubmed/31937768 http://dx.doi.org/10.1038/s41467-019-14116-y Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lu, Lihui Ren, Yuqi Yu, Tao Liu, Zhixiang Wang, Sice Tan, Lubin Zeng, Jiawei Feng, Qiru Lin, Rui Liu, Yang Guo, Qingchun Luo, Minmin Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus |
title | Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus |
title_full | Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus |
title_fullStr | Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus |
title_full_unstemmed | Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus |
title_short | Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus |
title_sort | control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959274/ https://www.ncbi.nlm.nih.gov/pubmed/31937768 http://dx.doi.org/10.1038/s41467-019-14116-y |
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