Leveraging interindividual variability in threat conditioning of inbred mice to model trait anxiety.


Journal

PLoS biology
ISSN: 1545-7885
Titre abrégé: PLoS Biol
Pays: United States
ID NLM: 101183755

Informations de publication

Date de publication:
28 May 2024
Historique:
received: 08 03 2024
accepted: 25 04 2024
medline: 28 5 2024
pubmed: 28 5 2024
entrez: 28 5 2024
Statut: aheadofprint

Résumé

Trait anxiety is a major risk factor for stress-induced and anxiety disorders in humans. However, animal models accounting for the interindividual variability in stress vulnerability are largely lacking. Moreover, the pervasive bias of using mostly male animals in preclinical studies poorly reflects the increased prevalence of psychiatric disorders in women. Using the threat imminence continuum theory, we designed and validated an auditory aversive conditioning-based pipeline in both female and male mice. We operationalised trait anxiety by harnessing the naturally occurring variability of defensive freezing responses combined with a model-based clustering strategy. While sustained freezing during prolonged retrieval sessions was identified as an anxiety-endophenotype biomarker in both sexes, females were consistently associated with an increased freezing response. RNA-sequencing of CeA, BLA, ACC, and BNST revealed massive differences in phasic and sustained responders' transcriptomes, correlating with transcriptomic signatures of psychiatric disorders, particularly post-traumatic stress disorder (PTSD). Moreover, we detected significant alterations in the excitation/inhibition balance of principal neurons in the lateral amygdala. These findings provide compelling evidence that trait anxiety in inbred mice can be leveraged to develop translationally relevant preclinical models to investigate mechanisms of stress susceptibility in a sex-specific manner.

Identifiants

pubmed: 38805548
doi: 10.1371/journal.pbio.3002642
pii: PBIOLOGY-D-24-00718
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e3002642

Informations de copyright

Copyright: © 2024 Kovlyagina et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Irina Kovlyagina (I)

Institute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Anna Wierczeiko (A)

Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Hristo Todorov (H)

Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Eric Jacobi (E)

Institute of Pathophysiology, and Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Margarita Tevosian (M)

Institute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Leibniz Institute for Resilience Research (LIR), Mainz, Germany.

Jakob von Engelhardt (J)

Institute of Pathophysiology, and Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Susanne Gerber (S)

Institute of Human Genetics, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Beat Lutz (B)

Institute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Leibniz Institute for Resilience Research (LIR), Mainz, Germany.

Classifications MeSH