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Post-stroke depression: exploring gut microbiota-mediated barrier dysfunction through immune regulation
Jia Jiang1, Haihua Xie2, Sihui Cao2
1The Second Affiliated Hospital, Hunan University of Chinese Medicine, Changsha, China.
Frontiers in Immunology
|March 18, 2025
Summary
Post-stroke depression (PSD) is common after ischemic stroke. This review explores how the gut microbiota, immune system, and gut barrier interact to influence PSD, offering new therapeutic insights.
Area of Science:
- Neuroscience
- Microbiology
- Immunology
Background:
- Post-stroke depression (PSD) affects over a third of ischemic stroke survivors.
- PSD is often underdiagnosed and undertreated, with limited effective interventions.
- The gut microbiota-gut-brain axis (MGBA) is increasingly recognized for its role in brain function.
Purpose of the Study:
- To systematically review the role of the microbiota-immune-barrier axis in post-stroke depression (PSD).
- To analyze how gut microbiota impacts gut barrier integrity and function post-ischemic stroke (IS).
- To explore potential therapeutic strategies for PSD targeting the MGBA.
Main Methods:
- Literature review focusing on the interplay between gut microbiota, immune responses, and gut barrier function in IS and PSD.
- Analysis of emerging evidence on the microbiota-gut-brain axis (MGBA) in cerebral ischemia.
- Exploration of current technologies for assessing MGBA and potential therapeutic interventions for PSD.
Main Results:
- Emerging evidence implicates the gut microbiota in regulating gut-brain communication relevant to PSD.
- The gut barrier plays a critical role in modulating inflammatory and immune responses post-IS.
- The proposed microbiota-immune-barrier axis offers a novel framework for understanding PSD pathophysiology.
Conclusions:
- The gut microbiota significantly influences gut barrier integrity and immune function after IS, potentially driving PSD.
- Understanding the microbiota-immune-barrier axis provides new insights into PSD mechanisms.
- Targeting the MGBA presents promising therapeutic avenues for preventing and treating PSD.
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