Prefrontal circuits encode both general danger and specific threat representations.


Journal

Nature neuroscience
ISSN: 1546-1726
Titre abrégé: Nat Neurosci
Pays: United States
ID NLM: 9809671

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 04 10 2022
accepted: 25 09 2023
medline: 4 12 2023
pubmed: 31 10 2023
entrez: 31 10 2023
Statut: ppublish

Résumé

Behavioral adaptation to potential threats requires both a global representation of danger to prepare the organism to react in a timely manner but also the identification of specific threatening situations to select the appropriate behavioral responses. The prefrontal cortex is known to control threat-related behaviors, yet it is unknown whether it encodes global defensive states and/or the identity of specific threatening encounters. Using a new behavioral paradigm that exposes mice to different threatening situations, we show that the dorsomedial prefrontal cortex (dmPFC) encodes a general representation of danger while simultaneously encoding a specific neuronal representation of each threat. Importantly, the global representation of danger persisted in error trials that instead lacked specific threat identity representations. Consistently, optogenetic prefrontal inhibition impaired overall behavioral performance and discrimination of different threatening situations without any bias toward active or passive behaviors. Together, these data indicate that the prefrontal cortex encodes both a global representation of danger and specific representations of threat identity to control the selection of defensive behaviors.

Identifiants

pubmed: 37904042
doi: 10.1038/s41593-023-01472-8
pii: 10.1038/s41593-023-01472-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2147-2157

Subventions

Organisme : Agence Nationale de la Recherche (French National Research Agency)
ID : ANR-10-EQPX-08 OPTOPATH

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature America, Inc.

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Auteurs

Mario Martin-Fernandez (M)

Université de Bordeaux, Neurocentre Magendie, U1215, Bordeaux, France. mario.martin-fernandez@inserm.fr.
INSERM, Neurocentre Magendie, U1215, Bordeaux, France. mario.martin-fernandez@inserm.fr.

Ana Paula Menegolla (AP)

Université de Bordeaux, Neurocentre Magendie, U1215, Bordeaux, France.
INSERM, Neurocentre Magendie, U1215, Bordeaux, France.

Guillem Lopez-Fernandez (G)

Université de Bordeaux, Neurocentre Magendie, U1215, Bordeaux, France.
INSERM, Neurocentre Magendie, U1215, Bordeaux, France.

Nanci Winke (N)

Université de Bordeaux, Neurocentre Magendie, U1215, Bordeaux, France.
INSERM, Neurocentre Magendie, U1215, Bordeaux, France.

Daniel Jercog (D)

Université de Bordeaux, Neurocentre Magendie, U1215, Bordeaux, France.
INSERM, Neurocentre Magendie, U1215, Bordeaux, France.

Ha-Rang Kim (HR)

Université de Bordeaux, Neurocentre Magendie, U1215, Bordeaux, France.
INSERM, Neurocentre Magendie, U1215, Bordeaux, France.

Delphine Girard (D)

Université de Bordeaux, Neurocentre Magendie, U1215, Bordeaux, France.
INSERM, Neurocentre Magendie, U1215, Bordeaux, France.

Cyril Dejean (C)

Université de Bordeaux, Neurocentre Magendie, U1215, Bordeaux, France.
INSERM, Neurocentre Magendie, U1215, Bordeaux, France.

Cyril Herry (C)

Université de Bordeaux, Neurocentre Magendie, U1215, Bordeaux, France. cyril.herry@inserm.fr.
INSERM, Neurocentre Magendie, U1215, Bordeaux, France. cyril.herry@inserm.fr.

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