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Linking emotional valence and anxiety in a mouse insula-amygdala circuit

Responses of the insular cortex (IC) and amygdala to stimuli of positive and negative valence are altered in patients with anxiety disorders. However, neural coding of both anxiety and valence by IC neurons remains unknown. Using fiber photometry recordings in mice, we uncover a selective increase o...

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Autores principales: Nicolas, C., Ju, A., Wu, Y., Eldirdiri, H., Delcasso, S., Couderc, Y., Fornari, C., Mitra, A., Supiot, L., Vérité, A., Masson, M., Rodriguez-Rozada, S., Jacky, D., Wiegert, J. S., Beyeler, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442438/
https://www.ncbi.nlm.nih.gov/pubmed/37604802
http://dx.doi.org/10.1038/s41467-023-40517-1
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author Nicolas, C.
Ju, A.
Wu, Y.
Eldirdiri, H.
Delcasso, S.
Couderc, Y.
Fornari, C.
Mitra, A.
Supiot, L.
Vérité, A.
Masson, M.
Rodriguez-Rozada, S.
Jacky, D.
Wiegert, J. S.
Beyeler, A.
author_facet Nicolas, C.
Ju, A.
Wu, Y.
Eldirdiri, H.
Delcasso, S.
Couderc, Y.
Fornari, C.
Mitra, A.
Supiot, L.
Vérité, A.
Masson, M.
Rodriguez-Rozada, S.
Jacky, D.
Wiegert, J. S.
Beyeler, A.
author_sort Nicolas, C.
collection PubMed
description Responses of the insular cortex (IC) and amygdala to stimuli of positive and negative valence are altered in patients with anxiety disorders. However, neural coding of both anxiety and valence by IC neurons remains unknown. Using fiber photometry recordings in mice, we uncover a selective increase of activity in IC projection neurons of the anterior (aIC), but not posterior (pIC) section, when animals are exploring anxiogenic spaces, and this activity is proportional to the level of anxiety of mice. Neurons in aIC also respond to stimuli of positive and negative valence, and the strength of response to strong negative stimuli is proportional to mice levels of anxiety. Using ex vivo electrophysiology, we characterized the IC connection to the basolateral amygdala (BLA), and employed projection-specific optogenetics to reveal anxiogenic properties of aIC-BLA neurons. Finally, we identified that aIC-BLA neurons are activated in anxiogenic spaces, as well as in response to aversive stimuli, and that both activities are positively correlated. Altogether, we identified a common neurobiological substrate linking negative valence with anxiety-related information and behaviors, which provides a starting point to understand how alterations of these neural populations contribute to psychiatric disorders.
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spelling pubmed-104424382023-08-23 Linking emotional valence and anxiety in a mouse insula-amygdala circuit Nicolas, C. Ju, A. Wu, Y. Eldirdiri, H. Delcasso, S. Couderc, Y. Fornari, C. Mitra, A. Supiot, L. Vérité, A. Masson, M. Rodriguez-Rozada, S. Jacky, D. Wiegert, J. S. Beyeler, A. Nat Commun Article Responses of the insular cortex (IC) and amygdala to stimuli of positive and negative valence are altered in patients with anxiety disorders. However, neural coding of both anxiety and valence by IC neurons remains unknown. Using fiber photometry recordings in mice, we uncover a selective increase of activity in IC projection neurons of the anterior (aIC), but not posterior (pIC) section, when animals are exploring anxiogenic spaces, and this activity is proportional to the level of anxiety of mice. Neurons in aIC also respond to stimuli of positive and negative valence, and the strength of response to strong negative stimuli is proportional to mice levels of anxiety. Using ex vivo electrophysiology, we characterized the IC connection to the basolateral amygdala (BLA), and employed projection-specific optogenetics to reveal anxiogenic properties of aIC-BLA neurons. Finally, we identified that aIC-BLA neurons are activated in anxiogenic spaces, as well as in response to aversive stimuli, and that both activities are positively correlated. Altogether, we identified a common neurobiological substrate linking negative valence with anxiety-related information and behaviors, which provides a starting point to understand how alterations of these neural populations contribute to psychiatric disorders. Nature Publishing Group UK 2023-08-21 /pmc/articles/PMC10442438/ /pubmed/37604802 http://dx.doi.org/10.1038/s41467-023-40517-1 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Nicolas, C.
Ju, A.
Wu, Y.
Eldirdiri, H.
Delcasso, S.
Couderc, Y.
Fornari, C.
Mitra, A.
Supiot, L.
Vérité, A.
Masson, M.
Rodriguez-Rozada, S.
Jacky, D.
Wiegert, J. S.
Beyeler, A.
Linking emotional valence and anxiety in a mouse insula-amygdala circuit
title Linking emotional valence and anxiety in a mouse insula-amygdala circuit
title_full Linking emotional valence and anxiety in a mouse insula-amygdala circuit
title_fullStr Linking emotional valence and anxiety in a mouse insula-amygdala circuit
title_full_unstemmed Linking emotional valence and anxiety in a mouse insula-amygdala circuit
title_short Linking emotional valence and anxiety in a mouse insula-amygdala circuit
title_sort linking emotional valence and anxiety in a mouse insula-amygdala circuit
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442438/
https://www.ncbi.nlm.nih.gov/pubmed/37604802
http://dx.doi.org/10.1038/s41467-023-40517-1
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