Skip to content
Open access

Social hierarchy shapes behavioral and transcriptional responses to chronic stress and ketamine in male mice

Jul 2026 · iScience · Vol 29, pp. 116825 · 0 citations · 45 references
Medicine

TL;DR

It is found that social hierarchy within a group strongly shapes stress outcomes, with dominant individuals exhibiting amplified behavioral alterations following chronic stress, including rest fragmentation and disrupted social interactions.

Abstract

Summary Chronic stress is a major risk factor for psychiatric disorders, yet the mechanisms underlying individual differences in vulnerability and treatment response remain poorly understood. Using the Social Box, a seminatural environment, we performed high-resolution, continuous tracking of group-housed male mice during 11 days, capturing behavior during both active and inactive phases. We found that social hierarchy within a group strongly shapes stress outcomes, with dominant individuals exhibiting amplified behavioral alterations following chronic stress, including rest fragmentation and disrupted social interactions. A single ketamine administration mitigated these effects, restoring baseline behavioral signatures in dominant individuals. Bulk mRNA sequencing was performed in the medial prefrontal cortex and ventral hippocampus. This revealed a hierarchy-dependent transcriptional response with 141 differentially expressed genes in the medial prefrontal cortex of dominant, ketamine-treated mice. Overall, this study provides a framework for examining stress and pharmacological interventions in group-housed mice, enabling high-resolution, longitudinal analyses under semi-naturalistic conditions.

Read PDF

Similar papers

Open access Aug 2026

Differential physiological, behavioral, and medial prefrontal cortex transcriptomic responses to chronic restraint stress between BALB/c and C57BL/6J mice

Chronic stress is a major risk factor for psychiatric disorders such as depression and anxiety, yet the biological basis of individual differences in stress susceptibility and resilience remains poorly understood. Here, we examined physiological, behavioral, and medial prefrontal cortex (mPFC) transcriptomic responses...

Taiga Kurihara, Aoi William Omi, Yuka Nakasone et al. · 0 citations
Open access Sep 2026

Sex-specific hippocampal trajectories induced by peripubertal and adult acute stress: proteomic profile, microglial alterations, neurogenic dysregulation, and depression-like behaviors

Findings indicate distinct sex- and timing-dependent patterns of behavioral and hippocampal response, involving neuroimmune, neurogenic, and proteomic changes that were not always accompanied by overt behavioral alterations.

P. Chaves-Peña, J. Munoz-Martin, M. I. Infantes-López et al. · 0 citations
Open access Sep 2026

495. Differential effects of social and non-social chronic stress on mPFC activity during cognitive processing

Abstract Background Cognitive impairment is a core feature of major depressive disorder and is associated with greater severity and resistance to antidepressant treatment. Dysfunction of the medial prefrontal cortex (mPFC), a region essential for cognitive control, emotional regulation, and motivational decision-making...

L. D. Godoy, F. Verza, G. Wegener et al. · 0 citations
Open access Sep 2026

Differential effects of acute, chronic, and social defeat stress on microglial morphology in the basolateral and central amygdala, and the medial and lateral habenula

Findings suggest that different stressors are associated with region- and subregion-dependent microglial remodelling, with the amygdala showing greater stress-related plasticity than the habenula.

A. Nieto-Quero, J. Munoz-Martin, M. I. Infantes-López et al. · 0 citations
Open access Sep 2026

499. Chronic stress impairs synaptic central metabolism in the prefrontal cortex, driving depression-related behaviors in mice

It is demonstrated that chronic stress disrupts central energy metabolism at prefrontal cortical synapses, driving to synaptic pathology and behavioral vulnerability and highlighting synaptic metabolic pathways as promising pharmacological targets for the treatment of stress-related psychiatric disorders.

H. Nagai, K. Ota, C. Numa et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.