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Chronic social defeat stress in female mice leads to sex-specific behavioral and neuroendocrine effects

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van Doeselaar,  Lotte
RG Stress Resilience, Max Planck Institute of Psychiatry, Max Planck Society;
IMPRS Translational Psychiatry, Max Planck Institute of Psychiatry, Max Planck Society;

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Yang,  Huanqing
RG Stress Resilience, Max Planck Institute of Psychiatry, Max Planck Society;

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Bordes,  Joeri
RG Stress Resilience, Max Planck Institute of Psychiatry, Max Planck Society;

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Brix,  Lea
RG Stress Resilience, Max Planck Institute of Psychiatry, Max Planck Society;
IMPRS Translational Psychiatry, Max Planck Institute of Psychiatry, Max Planck Society;

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Engelhardt,  Clara
Dept. Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Max Planck Society;

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Tang,  Fiona
RG Stress Resilience, Max Planck Institute of Psychiatry, Max Planck Society;

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Schmidt,  Mathias V.
RG Stress Resilience, Max Planck Institute of Psychiatry, Max Planck Society;

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Citation

van Doeselaar, L., Yang, H., Bordes, J., Brix, L., Engelhardt, C., Tang, F., et al. (2021). Chronic social defeat stress in female mice leads to sex-specific behavioral and neuroendocrine effects. STRESS-THE INTERNATIONAL JOURNAL ON THE BIOLOGY OF STRESS, 24(2), 168-180. doi:10.1080/10253890.2020.1864319.


Cite as: https://hdl.handle.net/21.11116/0000-0008-2768-8
Abstract
Over the years, it has become increasingly clear that males and females respond differently towards environmental stressors, highlighting the importance of including both sexes when studying the effects of stress. This study aims to provide further insight into the detailed consequences of exposing female mice to 21 days of chronic social defeat stress (CSDS). We used a protocol that relies on the ability of odorants and pheromones in male urine to trigger male mouse aggressive behavior. Collected male C57Bl/6n urine was applied to female C57Bl/6n mice who were then attacked by a novel male CD1 mouse each day according to the CDSD protocol. Control females were pair-housed and handled daily. Physiological, neuroendocrine and behavioral changes were evaluated during the experiment. CSDS exposure resulted in number of physiological changes, such as body weight gain, enlarged adrenals and reduced thymus weight, exaggerated HPA-axis negative feedback and increased anxiety-like behavior. However, no generalized social avoidance behavior was observed. This study provides important insights in the physiological, neuroendocrine and behavioral responses of female mice to CSDS, which are partially dependent on estrous cycle stage. This protocol will allow direct comparison of male and female responses to CSDS and enable sex-specific study of mechanisms underlying individual stress resilience. Lay summary
In this study we found that there are differences in the way that female and male mice respond towards chronic social stress conditions when it comes to behavior and hormonal changes.