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Gut microbiota is necessary for pair-housing to protect against post-stroke depression in mice
Su-Ting Jiang1, Yao-Huan Sun1, Ya Li2
1Department of Medical Care, School of Nursing, Nanjing University of Chinese Medicine, Nanjing 210023, China.
Abstract:
The goal of this study is to investigate the role of microbiota-gut-brain axis involved in the protective effect of pair-housing on post-stroke depression (PSD). PSD model was induced by occluding the middle cerebral artery (MCAO) plus restraint stress for four weeks. At three days after MCAO, the mice were restrained 2 h per day. For pair-housing (PH), each mouse was pair housed with a healthy isosexual cohabitor for four weeks. While in the other PH group, their drinking water was replaced with antibiotic water. On day 35 to day 40, anxiety- and depression-like behaviors (sucrose consumption, open field test, forced swim test, and tail-suspension test) were conducted. Results showed pair-housed mice had better performance on anxiety- and depression-like behaviors than the PSD mice, and the richness and diversity of intestinal flora were also improved. However, drinking antibiotic water reversed the effects of pair-housing. Furthermore, pair-housing had an obvious improvement in gut barrier disorder and inflammation caused by PSD. Particularly, they showed significant decreases in CD8 lymphocytes and mRNA levels of pro-inflammatory cytokines (TNF-a, IL-1β and IL-6), while IL-10 mRNA was upregulated. In addition, pair-housing significantly reduced activated microglia and increased Nissl's body in the hippocampus of PSD mice. However, all these improvements were worse in the pair-housed mice administrated with antibiotic water. We conclude that pair-housing significantly improves PSD in association with enhanced functions of microbiota-gut-brain axis, and homeostasis of gut microbiota is indispensable for the protective effect of pair-housing on PSD.
Insights
Pair-housing improves post-stroke depression (PSD) by enhancing the gut-brain axis. Maintaining gut microbiota balance is crucial for this protective effect, as antibiotics reversed the benefits.
Area of Science:
- Neuroscience
- Gastroenterology
- Immunology
Background:
- Post-stroke depression (PSD) is a common complication following stroke.
- The microbiota-gut-brain axis plays a role in mood regulation and neurological disorders.
Purpose of the Study:
- To investigate the protective role of pair-housing on post-stroke depression.
- To elucidate the involvement of the microbiota-gut-brain axis in the therapeutic effects of pair-housing.
Main Methods:
- A rat model of post-stroke depression was established using middle cerebral artery occlusion (MCAO) and restraint stress.
- Behavioral tests assessed depression and anxiety-like behaviors.
- Gut microbiota composition, gut barrier function, inflammation markers, and hippocampal changes were analyzed.
- Antibiotic treatment was used to assess the role of gut microbiota.
Main Results:
- Pair-housing significantly improved depression-like behaviors and normalized gut microbiota richness and diversity in PSD mice.
- Pair-housing reduced gut inflammation, decreased pro-inflammatory cytokines (TNF-α, IL-1β, IL-6), and increased IL-10.
- Pair-housing mitigated neuroinflammation by reducing activated microglia and increasing Nissl's bodies in the hippocampus.
- Antibiotic administration reversed the beneficial effects of pair-housing, indicating the critical role of gut microbiota.
Conclusions:
- Pair-housing exerts a protective effect against post-stroke depression.
- This effect is mediated through the modulation of the microbiota-gut-brain axis, including improvements in gut barrier function and immune responses.
- Gut microbiota homeostasis is essential for the therapeutic benefits of pair-housing in PSD.
Related Concept Videos
Introduction to the Human Microbiota
Development of Human Microbiota
The Oral Microbiota
Functions of the Gut Microbiota
Gut-Brain Axis
Microbiota of the Urogenital Tract

