Importance of fighting in the immune effects of social defeat
Abstract
Social defeat involves a clear physical component in the form of fight-induced injuries. The impact of body injuries on the immune response is not yet well known. In this study we compared the endocrine and immune responses to two types of social defeat in mice, one limiting the occurrence of skin injuries (mild social stress, MSS), and the other not (social disruption stress, SDR). In the two situations, six defeats were applied within 1 week. Plasma corticosterone and IL-6 levels were measured in blood samples taken after social defeat. Reactivity to LPS and sensitivity to corticosterone (CS) of spleen cells was assessed by measuring the in vitro production of cytokines (IL-6, IFN-gamma and IL-10) in response to LPS under a range of increasing concentrations of CS. The two types of stressors induced a similar plasma corticosterone response, but SDR mice showed significantly higher plasma IL-6 than MSS mice. Splenocytes from SDR but not from MSS mice produced more IL-6 and IL-10 in response to LPS and presented an altered responsiveness to CS in comparison to control mice. We conclude that the procedure involving fights and skin injuries was able to modulate the immune response in the spleen, whereas the procedure preventing the occurrence of fights did not. The increased immune reactivity observed in the fight-associated procedure could result from either a stronger psychological stress or a direct immune activation through the wounds.
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Animals injured during repeated social defeat exhibit glucocorticoid-resistant immune cells, systemic increases in glucocorticoids, exaggerated inflammatory responses, and increased pro-inflammatory gene expression in immune cells.
“Animals that sustain an injury during attack by the aggressor (Merlot et al., 2003) exhibit glucocorticoid resistant immune cells, systemic increases in glucocorticoids, exaggerated inflammatory responses (Avitsur et al., 2001; Stark et al., 2001), and increases in pro-inflammatory gene expression in immune cells (Powell et al., 2013).”
From Developmental psychoneuroendocrine and psychoneuroimmune pathways from childhood adversity to disease (2017) · cites this paper as Merlot et al., 2003
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References 56 · Cited by 43
- Authors
- Merlot, E., Moze, E., Dantzer, R., & Neveu, P. J.
- Affiliations
- Inserm (FR)
- ORCID
- Dantzer, Robert
- Venue
- Physiology & Behavior
- Publisher
- Elsevier BV
- Published
- 2003-11
- Volume
- 80
- Issue
- 2-3
- Pages
- 351-357
- ISSN
- 0031-9384 (ISSN-L)
- OpenAlex
- W1993140199
- Cited by
- 43
- References
- 56
- Citations by year
- 2025: 2 · 2023: 1 · 2021: 2 · 2020: 2 · 2019: 2 · 2018: 2 · 2017: 3 · 2016: 1 · 2015: 2 · 2013: 1 · 2012: 2
- FWCI
- 0.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Physiology & Behavior (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Health Sciences › Medicine › Psychiatry and Mental health › Cancer, Stress, Anesthesia, and Immune Response
- Keywords
- social defeat, social stress, immune response, corticosterone, interleukin-6, lipopolysaccharide, splenocytes, cytokine production, corticosteroid sensitivity, skin damage, psychological stress
- MeSH terms
- Analysis of Variance, Animals, Behavior, Animal, Conflict, Psychological, Corticosterone, Cytokinins, Dose-Response Relationship, Drug, Immunity, Interferon-gamma, Lipopolysaccharides, Male, Mice, Inbred BALB C, Radioimmunoassay, Random Allocation, Skin, Social Environment, Spleen, Stress, Psychological, Time Factors, Interleukin-6, Interleukin-10, Mice
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