Anxiety-related activity of ventral hippocampal interneurons.

Anxiety-related behaviour and activity Interneuron-pyramidal neuron interactions Trajectory-related activity Ventral hippocampus

Journal

Progress in neurobiology
ISSN: 1873-5118
Titre abrégé: Prog Neurobiol
Pays: England
ID NLM: 0370121

Informations de publication

Date de publication:
12 2022
Historique:
received: 02 05 2022
revised: 04 10 2022
accepted: 18 10 2022
pubmed: 24 10 2022
medline: 7 12 2022
entrez: 23 10 2022
Statut: ppublish

Résumé

Anxiety is an aversive mood reflecting the anticipation of potential threats. The ventral hippocampus (vH) is a key brain region involved in the genesis of anxiety responses. Recent studies have shown that anxiety is mediated by the activation of vH pyramidal neurons targeting various limbic structures. Throughout the cortex, the activity of pyramidal neurons is controlled by GABA-releasing inhibitory interneurons and the GABAergic system represents an important target of anxiolytic drugs. However, how the activity of vH inhibitory interneurons is related to different anxiety behaviours has not been investigated so far. Here, we integrated in vivo electrophysiology with behavioural phenotyping of distinct anxiety exploration behaviours in rats. We showed that pyramidal neurons and interneurons of the vH are selectively active when animals explore specific compartments of the elevated-plus-maze (EPM), an anxiety task for rodents. Moreover, rats with prior goal-related experience exhibited low-anxiety exploratory behaviour and showed a larger trajectory-related activity of vH interneurons during EPM exploration compared to high anxiety rats. Finally, in low anxiety rats, trajectory-related vH interneurons exhibited opposite activity to pyramidal neurons specifically in the open arms (i.e. more anxiogenic) of the EPM. Our results suggest that vH inhibitory micro-circuits could act as critical elements underlying different anxiety states.

Identifiants

pubmed: 36273721
pii: S0301-0082(22)00154-X
doi: 10.1016/j.pneurobio.2022.102368
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

102368

Subventions

Organisme : Austrian Science Fund FWF
ID : P 29588
Pays : Austria

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no competing interests.

Auteurs

Thomas Forro (T)

Laboratory of Systems Neuroscience, Department of Physiology, University of Bern, Bühlplatz 5, 3012 Bern, Switzerland. Electronic address: thomas.forro@unibe.ch.

Emmanouela Volitaki (E)

Laboratory of Systems Neuroscience, Department of Physiology, University of Bern, Bühlplatz 5, 3012 Bern, Switzerland.

Hugo Malagon-Vina (H)

Center for Brain Research, Division of Cognitive Neurobiology, Medical University of Vienna, Vienna 1090, Austria.

Thomas Klausberger (T)

Center for Brain Research, Division of Cognitive Neurobiology, Medical University of Vienna, Vienna 1090, Austria.

Thomas Nevian (T)

Neuronal Plasticity Group, Department of Physiology, University of Bern, Bühlplatz 5, 3012 Bern, Switzerland.

Stéphane Ciocchi (S)

Laboratory of Systems Neuroscience, Department of Physiology, University of Bern, Bühlplatz 5, 3012 Bern, Switzerland; Center for Brain Research, Division of Cognitive Neurobiology, Medical University of Vienna, Vienna 1090, Austria. Electronic address: stephane.ciocchi@unibe.ch.

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Classifications MeSH