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A circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding

Feeding behavior is regulated by both the homeostatic needs of the body and hedonic values of the food. Easy access to palatable energy-dense foods and the consequent obesity epidemic stress the urgent need for a better understanding of neural circuits that regulate hedonic feeding. Here, we report...

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Autores principales: Chen, Zijun, Chen, Gaowei, Zhong, Jiafeng, Jiang, Shaolei, Lai, Shishi, Xu, Hua, Deng, Xiaofei, Li, Fengling, Lu, Shanshan, Zhou, Kuikui, Li, Changlin, Liu, Zhongdong, Zhang, Xu, Zhu, Yingjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763109/
https://www.ncbi.nlm.nih.gov/pubmed/36028570
http://dx.doi.org/10.1038/s41380-022-01742-0
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author Chen, Zijun
Chen, Gaowei
Zhong, Jiafeng
Jiang, Shaolei
Lai, Shishi
Xu, Hua
Deng, Xiaofei
Li, Fengling
Lu, Shanshan
Zhou, Kuikui
Li, Changlin
Liu, Zhongdong
Zhang, Xu
Zhu, Yingjie
author_facet Chen, Zijun
Chen, Gaowei
Zhong, Jiafeng
Jiang, Shaolei
Lai, Shishi
Xu, Hua
Deng, Xiaofei
Li, Fengling
Lu, Shanshan
Zhou, Kuikui
Li, Changlin
Liu, Zhongdong
Zhang, Xu
Zhu, Yingjie
author_sort Chen, Zijun
collection PubMed
description Feeding behavior is regulated by both the homeostatic needs of the body and hedonic values of the food. Easy access to palatable energy-dense foods and the consequent obesity epidemic stress the urgent need for a better understanding of neural circuits that regulate hedonic feeding. Here, we report that neurotensin-positive neurons in the lateral septum (LS(Nts)) play a crucial role in regulating hedonic feeding. Silencing LS(Nts) specifically promotes feeding of palatable food, whereas activation of LS(Nts) suppresses overall feeding. LS(Nts) neurons project to the tuberal nucleus (TU) via GABA signaling to regulate hedonic feeding, while the neurotensin signal from LS(Nts)→the supramammillary nucleus (SUM) is sufficient to suppress overall feeding. In vivo calcium imaging and optogenetic manipulation reveal two populations of LS(Nts) neurons that are activated and inhibited during feeding, which contribute to food seeking and consumption, respectively. Chronic activation of LS(Nts) or LS(Nts)→TU is sufficient to reduce high-fat diet-induced obesity. Our findings suggest that LS(Nts)→TU is a key pathway in regulating hedonic feeding.
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spelling pubmed-97631092022-12-21 A circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding Chen, Zijun Chen, Gaowei Zhong, Jiafeng Jiang, Shaolei Lai, Shishi Xu, Hua Deng, Xiaofei Li, Fengling Lu, Shanshan Zhou, Kuikui Li, Changlin Liu, Zhongdong Zhang, Xu Zhu, Yingjie Mol Psychiatry Article Feeding behavior is regulated by both the homeostatic needs of the body and hedonic values of the food. Easy access to palatable energy-dense foods and the consequent obesity epidemic stress the urgent need for a better understanding of neural circuits that regulate hedonic feeding. Here, we report that neurotensin-positive neurons in the lateral septum (LS(Nts)) play a crucial role in regulating hedonic feeding. Silencing LS(Nts) specifically promotes feeding of palatable food, whereas activation of LS(Nts) suppresses overall feeding. LS(Nts) neurons project to the tuberal nucleus (TU) via GABA signaling to regulate hedonic feeding, while the neurotensin signal from LS(Nts)→the supramammillary nucleus (SUM) is sufficient to suppress overall feeding. In vivo calcium imaging and optogenetic manipulation reveal two populations of LS(Nts) neurons that are activated and inhibited during feeding, which contribute to food seeking and consumption, respectively. Chronic activation of LS(Nts) or LS(Nts)→TU is sufficient to reduce high-fat diet-induced obesity. Our findings suggest that LS(Nts)→TU is a key pathway in regulating hedonic feeding. Nature Publishing Group UK 2022-08-26 2022 /pmc/articles/PMC9763109/ /pubmed/36028570 http://dx.doi.org/10.1038/s41380-022-01742-0 Text en © The Author(s) 2022 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
Chen, Zijun
Chen, Gaowei
Zhong, Jiafeng
Jiang, Shaolei
Lai, Shishi
Xu, Hua
Deng, Xiaofei
Li, Fengling
Lu, Shanshan
Zhou, Kuikui
Li, Changlin
Liu, Zhongdong
Zhang, Xu
Zhu, Yingjie
A circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding
title A circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding
title_full A circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding
title_fullStr A circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding
title_full_unstemmed A circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding
title_short A circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding
title_sort circuit from lateral septum neurotensin neurons to tuberal nucleus controls hedonic feeding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763109/
https://www.ncbi.nlm.nih.gov/pubmed/36028570
http://dx.doi.org/10.1038/s41380-022-01742-0
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