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A bottom-up reward pathway mediated by somatostatin neurons in the medial septum complex underlying appetitive learning

Valence detection and processing are essential for the survival of animals and their life quality in complex environments. Neural circuits underlying the transformation of external sensory signals into positive valence coding to generate appropriate behavioral responses remain not well-studied. Here...

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Autores principales: Shen, Li, Zhang, Guang-Wei, Tao, Can, Seo, Michelle B., Zhang, Nicole K., Huang, Junxiang J., Zhang, Li I., Tao, Huizhong W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901785/
https://www.ncbi.nlm.nih.gov/pubmed/35256596
http://dx.doi.org/10.1038/s41467-022-28854-z
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author Shen, Li
Zhang, Guang-Wei
Tao, Can
Seo, Michelle B.
Zhang, Nicole K.
Huang, Junxiang J.
Zhang, Li I.
Tao, Huizhong W.
author_facet Shen, Li
Zhang, Guang-Wei
Tao, Can
Seo, Michelle B.
Zhang, Nicole K.
Huang, Junxiang J.
Zhang, Li I.
Tao, Huizhong W.
author_sort Shen, Li
collection PubMed
description Valence detection and processing are essential for the survival of animals and their life quality in complex environments. Neural circuits underlying the transformation of external sensory signals into positive valence coding to generate appropriate behavioral responses remain not well-studied. Here, we report that somatostatin (SOM) subtype of GABAergic neurons in the mouse medial septum complex (MS), but not parvalbumin subtype or glutamatergic neurons, specifically encode reward signals and positive valence. Through an ascending pathway from the nucleus of solitary tract and then parabrachial nucleus, the MS SOM neurons receive rewarding taste signals and suppress the lateral habenula. They contribute essentially to appetitive associative learning via their projections to the lateral habenula: learning enhances their responses to reward-predictive sensory cues, and suppressing their responses to either conditioned or unconditioned stimulus impairs acquisition of reward learning. Thus, MS serves as a critical hub for transforming bottom-up sensory signals to mediate appetitive behaviors.
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spelling pubmed-89017852022-03-23 A bottom-up reward pathway mediated by somatostatin neurons in the medial septum complex underlying appetitive learning Shen, Li Zhang, Guang-Wei Tao, Can Seo, Michelle B. Zhang, Nicole K. Huang, Junxiang J. Zhang, Li I. Tao, Huizhong W. Nat Commun Article Valence detection and processing are essential for the survival of animals and their life quality in complex environments. Neural circuits underlying the transformation of external sensory signals into positive valence coding to generate appropriate behavioral responses remain not well-studied. Here, we report that somatostatin (SOM) subtype of GABAergic neurons in the mouse medial septum complex (MS), but not parvalbumin subtype or glutamatergic neurons, specifically encode reward signals and positive valence. Through an ascending pathway from the nucleus of solitary tract and then parabrachial nucleus, the MS SOM neurons receive rewarding taste signals and suppress the lateral habenula. They contribute essentially to appetitive associative learning via their projections to the lateral habenula: learning enhances their responses to reward-predictive sensory cues, and suppressing their responses to either conditioned or unconditioned stimulus impairs acquisition of reward learning. Thus, MS serves as a critical hub for transforming bottom-up sensory signals to mediate appetitive behaviors. Nature Publishing Group UK 2022-03-07 /pmc/articles/PMC8901785/ /pubmed/35256596 http://dx.doi.org/10.1038/s41467-022-28854-z 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
Shen, Li
Zhang, Guang-Wei
Tao, Can
Seo, Michelle B.
Zhang, Nicole K.
Huang, Junxiang J.
Zhang, Li I.
Tao, Huizhong W.
A bottom-up reward pathway mediated by somatostatin neurons in the medial septum complex underlying appetitive learning
title A bottom-up reward pathway mediated by somatostatin neurons in the medial septum complex underlying appetitive learning
title_full A bottom-up reward pathway mediated by somatostatin neurons in the medial septum complex underlying appetitive learning
title_fullStr A bottom-up reward pathway mediated by somatostatin neurons in the medial septum complex underlying appetitive learning
title_full_unstemmed A bottom-up reward pathway mediated by somatostatin neurons in the medial septum complex underlying appetitive learning
title_short A bottom-up reward pathway mediated by somatostatin neurons in the medial septum complex underlying appetitive learning
title_sort bottom-up reward pathway mediated by somatostatin neurons in the medial septum complex underlying appetitive learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901785/
https://www.ncbi.nlm.nih.gov/pubmed/35256596
http://dx.doi.org/10.1038/s41467-022-28854-z
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