Vulnerability to chronic subordination stress-induced depression-like disorders in adult 129SvEv male mice
Abstract
Exposure to stressful life events is intimately linked with vulnerability to neuropsychiatric disorders such as major depression. Pre-clinical animal models offer an effective tool to disentangle the underlying molecular mechanisms. In particular, the 129SvEv strain is often used to develop transgenic mouse models but poorly characterized as far as behavior and neuroendocrine functions are concerned. Here we present a comprehensive characterization of 129SvEv male mice's vulnerability to social stress-induced depression-like disorders and physiological comorbidities. We employed a well characterized mouse model of chronic social stress based on social defeat and subordination. Subordinate 129SvEv mice showed body weight gain, hyperphagia, increased adipose fat pads weight and basal plasma corticosterone. Home cage phenotyping revealed a suppression of spontaneous locomotor activity and transient hyperthermia. Subordinate 129SvEv mice also showed marked fearfulness, anhedonic-like response toward a novel but palatable food, increased anxiety in the elevated plus maze and social avoidance of an unfamiliar male mouse. A direct measured effect of the stressfulness of the living environment, i.e. the amount of daily aggression received, predicted the degree of corticosterone level and locomotor activity but not of the other parameters. This is the first study validating a chronic subordination stress paradigm in 129SvEv male mice. Results demonstrated remarkable stress vulnerabili…
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The C57BL/6J line appears to be less susceptible to stress when compared with other strains.
“Of note, a series of recent papers suggests that the C57BL/6J line appears to be less susceptible to stress when compared with other strains39–41.”
From A standardized protocol for repeated social defeat stress in mice (2011) · cites this paper as [39]
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A standardized protocol for repeated social defeat stress in mice
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Self-citationDefeat stress in rodents: from behavior to molecules
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- Authors
- Dadomo, H., Sanghez, V., Di Cristo, L., Lori, A., Ceresini, G., Malinge, I., Parmigiani, S., Palanza, P., Sheardown, M., & Bartolomucci, A.
- Affiliations
- University of Parma (IT)
- Takeda (United Kingdom) (GB)
- Corresponding author
- Bartolomucci, Alessandro
- ORCID
- Venue
- Progress in Neuro-Psychopharmacology and Biological Psychiatry
- Publisher
- Elsevier BV
- Published
- 2011-08
- Volume
- 35
- Issue
- 6
- Pages
- 1461-1471
- ISSN
- 0278-5846 (ISSN-L)
- OpenAlex
- W2119386934
- Cited by
- 54
- References
- 8
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 2 · 2023: 3 · 2022: 4 · 2021: 4 · 2020: 5 · 2019: 4 · 2018: 4 · 2017: 4 · 2016: 3 · 2015: 4 · 2014: 7 · 2013: 2 · 2012: 3
- FWCI
- 1.10
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Progress in Neuro-Psychopharmacology and Biological Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Keywords
- social defeat, depression-like behavior, stress vulnerability, corticosterone, hyperphagia, adipose tissue, locomotor activity, anhedonia, anxiety, social avoidance, aggression, mouse model of depression
- MeSH terms
- Aggression, Animals, Anxiety, Chronic Disease, Corticosterone, Depression, Disease Models, Animal, Dominance-Subordination, Fever, Hyperphagia, Male, Motor Activity, Social Behavior, Stress, Psychological, Weight Gain, Mice, Mice, 129 Strain
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