# Gut Microbiota and Exercise-Induced Fatigue: A Narrative Review of Mechanisms, Nutritional Interventions, and Future Directions

**Authors:** Zhengxin Zhao, Shengwei Zhao, Wenli Li, Zheng Lai, Yang Zhou, Feng Guan, Xu Liang, Jiawei Zhang, Linding Wang

PMC · DOI: 10.3390/nu18030502 · Nutrients · 2026-02-02

## TL;DR

This review explores how gut microbes influence exercise-induced fatigue and how nutrition can help manage it.

## Contribution

The paper identifies four microbiota-mediated pathways linking gut health to exercise fatigue and suggests targeted nutrition as a recovery strategy.

## Key findings

- High-intensity exercise disrupts gut homeostasis, altering microbial communities and increasing intestinal permeability.
- Microbiota influences fatigue through energy metabolism, inflammation, gut barrier function, and brain signaling.
- Probiotics, prebiotics, and bioactive compounds may improve fatigue biomarkers and endurance, but effects vary by context.

## Abstract

Background: Exercise-induced fatigue (EIF) impairs performance and recovery and may contribute to overreaching/overtraining and adverse health outcomes. Beyond classical explanations (substrate depletion, metabolite accumulation, oxidative stress), accumulating evidence indicates that the gut microbiota modulates fatigue-related physiology through metabolic, immune, barrier, and neurobehavioral pathways. Methods: We conducted a structured narrative review of PubMed and Web of Science covering 1 January 2015 to 30 November 2025 using predefined keywords related to EIF, gut microbiota, recovery, and nutritional interventions. Human studies, animal experiments, and mechanistic preclinical work (in vivo/in vitro) were included when they linked exercise load, microbial features (taxa/functions/metabolites), and fatigue-relevant outcomes. Results: Across models, high-intensity or prolonged exercise is consistently associated with disrupted gut homeostasis, including altered community structure, reduced abundance of beneficial taxa, increased intestinal permeability, and shifts in microbial metabolites (e.g., short-chain fatty acids). Evidence converges on four interconnected microbiota-mediated pathways relevant to EIF: (1) energy availability and metabolic by-product clearance; (2) redox balance and inflammation; (3) intestinal barrier integrity and endotoxemia risk; and (4) central fatigue and exercise motivation via microbiota–gut–brain signaling. Nutritional strategies—particularly targeted probiotics, prebiotics/plant polysaccharides, and selected bioactive compounds—show potential to improve fatigue biomarkers and endurance-related outcomes, although effects appear context-dependent (exercise modality, baseline fitness, diet, and baseline microbiota). Conclusions: Current evidence supports a mechanistic role of the gut microbiota in EIF and highlights microbiota-targeted nutrition as a promising adjunct for recovery optimization. Future work should prioritize causal validation (e.g., fecal microbiota transplantation and metabolite supplementation), athlete-focused randomized trials with standardized fatigue endpoints, and precision approaches that stratify individuals by baseline microbiome features and training load.

## Full-text entities

- **Diseases:** EIF (MESH:D000092202), inflammation (MESH:D007249), endotoxemia (MESH:D019446), Fatigue (MESH:D005221)
- **Chemicals:** prebiotics (MESH:D056692), polysaccharides (MESH:D011134), short-chain fatty acids (MESH:D005232)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

79 references — full list in the complete paper: https://tomesphere.com/paper/PMC12899331/full.md

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Source: https://tomesphere.com/paper/PMC12899331