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Updated: Jul 21, 2025

A Gut-on-a-Chip Model to Study the Gut Microbiome-Nervous System Axis
Published on: July 28, 2023
The Gut-Brain Axis as a Therapeutic Target in Multiple Sclerosis
Ana Maria Buga1, Vlad Padureanu2, Anca-Lelia Riza3,4
1Department of Biochemistry, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
Targeting gut microbiota may help manage multiple sclerosis (MS) by reducing oxidative stress and neuroinflammation. Future clinical trials need larger cohorts and longer observation periods for validation.
Area of Science:
- Neuroscience
- Immunology
- Microbiology
Background:
- The central nervous system (CNS) is vulnerable to oxidative stress.
- Gut microbiota dysbiosis can trigger oxidative damage, leading to mitochondrial dysfunction, neuroinflammation, and neurodegeneration.
- The gut-brain axis plays a critical role in mediating these processes, particularly in multiple sclerosis (MS).
Purpose of the Study:
- To review recent findings on oxidative-stress-related inflammation mediated by the gut-brain axis in MS.
- To summarize existing clinical trials targeting microbiota-related oxidative stress for MS management.
- To identify suitable interventions, combinations, and timings for microbiota-based therapies.
Main Methods:
- Evidence-based review of existing clinical trials.
- Analysis of studies focusing on gut microbiota interventions in MS.
- Assessment of trial designs, cohort sizes, and MS subtypes studied.
Main Results:
- Growing evidence supports targeting the gut microbiota as a promising strategy for MS management.
- Most reviewed trials focused on relapsing-remitting MS (RRMS), with limited data on other MS stages like secondary progressive MS (SPMS).
- Significant heterogeneity in study designs and outcomes highlights the need for standardized, large-scale clinical validation.
Conclusions:
- Gut microbiota modulation represents a potential therapeutic avenue for MS.
- Further research and well-designed clinical trials with larger cohorts and extended follow-up are essential.
- Future trials should consider early life interventions and long-term monitoring to capture complex intersystem interactions.
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