Chronic subordinate colony housing paradigm: a mouse model for mechanisms of PTSD vulnerability, targeted prevention, and treatment-2016 Curt Richter Award Paper
Abstract
There is considerable individual variability in vulnerability for developing posttraumatic stress disorder (PTSD); evidence suggests that this variability is related in part to genetic and environmental factors, including adverse early life experience. Interestingly, recent studies indicate that induction of chronic low-grade inflammation may be a common mechanism underlying gene and environment interactions that increase the risk for development of PTSD symptoms, and, therefore, may be a target for novel interventions for prevention or treatment of PTSD. Development of murine models with face, construct, and predictive validity would provide opportunities to investigate in detail complex genetic, environmental, endocrine, and immunologic factors that determine vulnerability to PTSD-like syndromes, and furthermore may provide mechanistic insight leading to development of novel interventions for both prevention and treatment of PTSD symptoms. Here we describe the potential use of the chronic subordinate colony housing (CSC) paradigm in mice as an adequate animal model for development of a PTSD-like syndrome and describe recent studies that suggest novel interventions for the prevention and treatment of PTSD.
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In a murine model of PTSD, immunization with a heat-killed preparation of Mycobacterium vaccae induced a more proactive behavioral response to a psychosocial stressor.
“A study using a murine model of PTSD (170) has demonstrated that immunization with a heat-killed preparation of the immunoregulatory bacterium Mycobacterium vaccae (NCTC 11659) induced a more proactive behavioral response to a psychosocial stressor (171).”
From Vagus Nerve as Modulator of the Brain–Gut Axis in Psychiatric and Inflammatory Disorders (2018) · cites this paper as [170]
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Chronic psychosocial stress disturbs long-bone growth in adolescent mice
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Animal models of social stress: the dark side of social interactions
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Splenic glucocorticoid resistance following psychosocial stress requires physical injury
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Self-citationWu, H., Song, Y., Li, J., Lei, X., Zhang, S., Gao, Y., Cheng, P., Liu, B., Miao, S., Bi, L., et al. (2019) · Cell Proliferation · doi:10.1111/cpr.12725 · Cited by 39 · see citing works
Neutrophil-derived catecholamines mediate negative stress effects on bone
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Potential causal association between gut microbiome and posttraumatic stress disorder
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Foxx, C. L., Heinze, J. D., González, A., Vargas, F., Baratta, M. V., Elsayed, A. I., Stewart, J. R., Loupy, K. M., Arnold, M. R., Flux, M. C., et al. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2020.524833 · Cited by 29 · see citing works
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Self-citationEffects of Prior Psychosocial Trauma on Subsequent Immune Response After Experimental Thorax Trauma
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The Impact of Stressor Exposure and Glucocorticoids on Anxiety and Fear
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- Authors
- Reber, S. O., Langgartner, D., Foertsch, S., Postolache, T. T., Brenner, L. A., Guendel, H., & Lowry, C. A.
- Affiliations
- Universität Ulm (DE)
- University of Maryland, Baltimore (US)
- Mental Illness Research, Education and Clinical Centers (US)
- University of Colorado Boulder (US)
- Corresponding author
- Reber, Stefan O.
- ORCID
- Venue
- Psychoneuroendocrinology
- Publisher
- Elsevier BV
- Published
- 2016-12
- Volume
- 74
- Pages
- 221-230
- ISSN
- 0306-4530 (ISSN-L)
- OpenAlex
- W2430306692
- Cited by
- 59
- References
- 102
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 2 · 2023: 6 · 2022: 10 · 2021: 7 · 2020: 7 · 2019: 7 · 2018: 8 · 2017: 5
- FWCI
- 0.99
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Psychoneuroendocrinology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- the German Research Foundation (2911/2-1, RE 2911/5-1)
- the Department of the Navy, Office of Naval Research Multidisciplinary University Research Initiative (MURI) Award (N00014-15-1-2809)
- National Institutes of Health (DA019921)
- Department of Veterans Affairs Office of Research and Development (RX002232-01)
- Colorado Clinical & Translational Sciences Institute (CCTSI) Center for Neuroscience (CNSTT-15-145)
- Colorado Department of Public Health and Environment (DCEED-3510)
- the Alfred P. Sloan Foundation (G‐2015‐14165, 2016-7077)
- Topics
- Social Sciences › Psychology › Clinical Psychology › Posttraumatic Stress Disorder Research
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Social Sciences › Psychology › Clinical Psychology › Child Abuse and Trauma
- Keywords
- post-traumatic stress disorder, mouse model, gut dysbiosis, low-grade inflammation, Mycobacterium vaccae, preimmunization, stress resilience, trauma vulnerability, gene-environment interaction, PTSD prevention, PTSD treatment
- MeSH terms
- Animals, Disease Models, Animal, Housing, Animal, Inflammation, Stress Disorders, Post-Traumatic, Mice, Dysbiosis
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