Depression, anxiety-like behavior and memory impairment are associated with increased oxidative stress and inflammation in a rat model of social stress
Open accessAbstract
In the present study, we have examined the behavioral and biochemical effect of induction of psychological stress using a modified version of the resident-intruder model for social stress (social defeat). At the end of the social defeat protocol, body weights, food and water intake were recorded, depression and anxiety-like behaviors as well as memory function was examined. Biochemical analysis including oxidative stress measurement, inflammatory markers and other molecular parameters, critical to behavioral effects were examined. We observed a significant decrease in the body weight in the socially defeated rats as compared to the controls. Furthermore, social defeat increased anxiety-like behavior and caused memory impairment in rats (P<0.05). Socially defeated rats made significantly more errors in long term memory tests (P<0.05) as compared to control rats. Furthermore, brain extracellular signal-regulated kinase-1/2 (ERK1/2), and an inflammatory marker, interleukin (IL)-6 were activated (P<0.05), while the protein levels of glyoxalase (GLO)-1, glutathione reductase (GSR)-1, calcium/calmodulin-dependent protein kinase type (CAMK)-IV, cAMP-response-element-binding protein (CREB) and brain-derived neurotrophic factor (BDNF) were significantly less (P<0.05) in the hippocampus, but not in the prefrontal cortex and amygdala of socially defeated rats, when compared to control rats. We suggest that social defeat stress alters ERK1/2, IL-6, GLO1, GSR1, CAMKIV, CREB, and BDNF levels in specific brain areas, leading to oxidative stress-induced anxiety-depression-like behaviors and as well as memory impairment in rats.
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Oxidative unbalance was demonstrated in anxiety models by increased lipid peroxidation, protein carboxylation, and protein thiol oxidation and decreased vitamin E levels.
“Oxidative unbalance was also demonstrated in anxiety models by mainly pointing out the presence of increased lipid peroxidation, protein carboxylation, and protein thiol oxidation and decreased vitamin E levels [109, 173].”
From Oxidative Stress Implications in the Affective Disorders: Main Biomarkers, Animal Models Relevance, Genetic Perspectives, and Antioxidant Approaches (2016) · cites this paper as [173]
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References 88 · Cited by 380
- Authors
- Patki, G., Solanki, N., Atrooz, F., Allam, F., & Salim, S.
- Affiliations
- University of Houston (US)
- Corresponding author
- Salim, Samina
- Venue
- Brain Research
- Publisher
- Elsevier BV
- Published
- 2013-11
- Volume
- 1539
- Pages
- 73-86
- ISSN
- 0006-8993 (ISSN-L)
- PMC
- PMC4316676
- OpenAlex
- W1974409272
- Cited by
- 380
- References
- 88
- Citations by year
- 2026: 8 · 2025: 22 · 2024: 26 · 2023: 17 · 2022: 44 · 2021: 47 · 2020: 43 · 2019: 38 · 2018: 34 · 2017: 21 · 2016: 31 · 2015: 23 · 2014: 26
- FWCI
- 12.09
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH (R15 G103327)
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- social defeat stress, social stress, depression, anxiety-like behavior, memory impairment, oxidative stress, neuroinflammation, interleukin-6, ERK1/2, glyoxalase I, glutathione reductase, CaMKIV, CREB, brain-derived neurotrophic factor, hippocampus, long-term memory
- MeSH terms
- Animals, Anxiety, Brain, Depression, Disease Models, Animal, Inflammation, Male, Memory Disorders, Social Dominance, Stress, Psychological, Rats, Sprague-Dawley, Oxidative Stress, Rats, Long-Evans, Rats
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