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

• Published in: Molecular psychiatry Vol. 27; no. 12; pp. 4843 - 4860
• Main Authors: 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
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.12.2022; Nature Publishing Group
• Subjects: 13/51; 14/32; 631/378; 631/443; 64/60; 9/74; Animal cognition; Animals; Behavioral Sciences; Biological Psychology; Brain diseases; Brain research; Calcium imaging; Dopamine; Experiments; Feeding behavior; Feeding Behavior - physiology; Food; Food consumption; Genetic engineering; Hedonic response; High fat diet; Hypothalamic Area, Lateral - physiology; Laboratory animals; Medicine; Medicine & Public Health; Metabolic disorders; Mice; Neural networks; Neurons; Neurons - metabolism; Neurosciences; Neurotensin; Neurotensin - metabolism; Obesity; Obesity - metabolism; Pharmacotherapy; Psychiatry; Science; Septum; γ-Aminobutyric acid
• ISSN: 1359-4184; 1476-5578
• DOI: 10.1038/s41380-022-01742-0

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.