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The tectonigral pathway regulates appetitive locomotion in predatory hunting in mice
Appetitive locomotion is essential for animals to approach rewards, such as food and prey. The neuronal circuitry controlling appetitive locomotion is unclear. In a goal-directed behavior—predatory hunting, we show an excitatory brain circuit from the superior colliculus (SC) to the substantia nigra...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292483/ https://www.ncbi.nlm.nih.gov/pubmed/34285209 http://dx.doi.org/10.1038/s41467-021-24696-3 |
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author | Huang, Meizhu Li, Dapeng Cheng, Xinyu Pei, Qing Xie, Zhiyong Gu, Huating Zhang, Xuerong Chen, Zijun Liu, Aixue Wang, Yi Sun, Fangmiao Li, Yulong Zhang, Jiayi He, Miao Xie, Yuan Zhang, Fan Qi, Xiangbing Shang, Congping Cao, Peng |
author_facet | Huang, Meizhu Li, Dapeng Cheng, Xinyu Pei, Qing Xie, Zhiyong Gu, Huating Zhang, Xuerong Chen, Zijun Liu, Aixue Wang, Yi Sun, Fangmiao Li, Yulong Zhang, Jiayi He, Miao Xie, Yuan Zhang, Fan Qi, Xiangbing Shang, Congping Cao, Peng |
author_sort | Huang, Meizhu |
collection | PubMed |
description | Appetitive locomotion is essential for animals to approach rewards, such as food and prey. The neuronal circuitry controlling appetitive locomotion is unclear. In a goal-directed behavior—predatory hunting, we show an excitatory brain circuit from the superior colliculus (SC) to the substantia nigra pars compacta (SNc) to enhance appetitive locomotion in mice. This tectonigral pathway transmits locomotion-speed signals to dopamine neurons and triggers dopamine release in the dorsal striatum. Synaptic inactivation of this pathway impairs appetitive locomotion but not defensive locomotion. Conversely, activation of this pathway increases the speed and frequency of approach during predatory hunting, an effect that depends on the activities of SNc dopamine neurons. Together, these data reveal that the SC regulates locomotion-speed signals to SNc dopamine neurons to enhance appetitive locomotion in mice. |
format | Online Article Text |
id | pubmed-8292483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82924832021-07-23 The tectonigral pathway regulates appetitive locomotion in predatory hunting in mice Huang, Meizhu Li, Dapeng Cheng, Xinyu Pei, Qing Xie, Zhiyong Gu, Huating Zhang, Xuerong Chen, Zijun Liu, Aixue Wang, Yi Sun, Fangmiao Li, Yulong Zhang, Jiayi He, Miao Xie, Yuan Zhang, Fan Qi, Xiangbing Shang, Congping Cao, Peng Nat Commun Article Appetitive locomotion is essential for animals to approach rewards, such as food and prey. The neuronal circuitry controlling appetitive locomotion is unclear. In a goal-directed behavior—predatory hunting, we show an excitatory brain circuit from the superior colliculus (SC) to the substantia nigra pars compacta (SNc) to enhance appetitive locomotion in mice. This tectonigral pathway transmits locomotion-speed signals to dopamine neurons and triggers dopamine release in the dorsal striatum. Synaptic inactivation of this pathway impairs appetitive locomotion but not defensive locomotion. Conversely, activation of this pathway increases the speed and frequency of approach during predatory hunting, an effect that depends on the activities of SNc dopamine neurons. Together, these data reveal that the SC regulates locomotion-speed signals to SNc dopamine neurons to enhance appetitive locomotion in mice. Nature Publishing Group UK 2021-07-20 /pmc/articles/PMC8292483/ /pubmed/34285209 http://dx.doi.org/10.1038/s41467-021-24696-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Huang, Meizhu Li, Dapeng Cheng, Xinyu Pei, Qing Xie, Zhiyong Gu, Huating Zhang, Xuerong Chen, Zijun Liu, Aixue Wang, Yi Sun, Fangmiao Li, Yulong Zhang, Jiayi He, Miao Xie, Yuan Zhang, Fan Qi, Xiangbing Shang, Congping Cao, Peng The tectonigral pathway regulates appetitive locomotion in predatory hunting in mice |
title | The tectonigral pathway regulates appetitive locomotion in predatory hunting in mice |
title_full | The tectonigral pathway regulates appetitive locomotion in predatory hunting in mice |
title_fullStr | The tectonigral pathway regulates appetitive locomotion in predatory hunting in mice |
title_full_unstemmed | The tectonigral pathway regulates appetitive locomotion in predatory hunting in mice |
title_short | The tectonigral pathway regulates appetitive locomotion in predatory hunting in mice |
title_sort | tectonigral pathway regulates appetitive locomotion in predatory hunting in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292483/ https://www.ncbi.nlm.nih.gov/pubmed/34285209 http://dx.doi.org/10.1038/s41467-021-24696-3 |
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