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


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
21 08 2023
Historique:
received: 15 04 2023
accepted: 01 08 2023
medline: 23 8 2023
pubmed: 22 8 2023
entrez: 21 8 2023
Statut: epublish

Résumé

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.

Identifiants

pubmed: 37604802
doi: 10.1038/s41467-023-40517-1
pii: 10.1038/s41467-023-40517-1
pmc: PMC10442438
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5073

Informations de copyright

© 2023. Springer Nature Limited.

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Auteurs

C Nicolas (C)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

A Ju (A)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

Y Wu (Y)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

H Eldirdiri (H)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

S Delcasso (S)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

Y Couderc (Y)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

C Fornari (C)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

A Mitra (A)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

L Supiot (L)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

A Vérité (A)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

M Masson (M)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

S Rodriguez-Rozada (S)

Research Group Synaptic Wiring and Information Processing, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

D Jacky (D)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France.

J S Wiegert (JS)

Research Group Synaptic Wiring and Information Processing, Center for Molecular Neurobiology Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

A Beyeler (A)

Neurocentre Magendie, INSERM 1215, Université de Bordeaux, Bordeaux, France. anna.beyeler@inserm.fr.

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Classifications MeSH