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Chronic cohabitation with CD1 male mice induces anxiety-like behaviors, reduced spontaneous alternation, dysregulated HPA axis, and disrupted sleep architecture in C57BL/6J female mice.

Created on 04 Oct 2026

Authors

Yan Yang, Maozeng Yang, Zhiping Cao, Yong Xu

Published in

Brain research. Pages 150567. Oct 03, 2026. Epub Oct 03, 2026.

Abstract

In contrast to the well-documented phenomena of inter-male aggression and competition in nature, the long-term consequences for females involuntarily exposed to persistent male-initiated social threat remain inadequately understood. In the present study, we demonstrate that C57BL/6J female mice co-housed with CD1 male mice for 14 days developed anxiety-like behaviors and cognitive deficits, without exhibiting depressive-like phenotypes. Concurrently, these females displayed a significant decrease in serum estrogen levels and dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis. Furthermore, co-housing with CD1 males profoundly disrupted sleep architecture in C57BL/6J females, as evidenced by reduced wakefulness and prolonged durations of both non-rapid eye movement (NREM) and rapid eye movement (REM) sleep. Mechanistically, these behavioral and physiological alterations were associated with substantial a reduction in cell density in the CA1 and CA3 subregions of the ventral hippocampus, accompanied by a marked downregulation of brain-derived neurotrophic factor (BDNF) within these same areas. Collectively, our findings provide experimental evidence for the adverse effects of chronic exposure to persistent male-initiated social threat on female recipients in a mammalian model, thereby offering a theoretical framework for understanding the enduring psychological trauma that may arise from sustained environments of psychological harassment, domestic violence, or sexual coercion-circumstances frequently encountered by women in human society.

PMID:
42829061
Bibliographic data and abstract were imported from PubMed on 04 Oct 2026.

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