» Articles » PMID: 28579962

The Crosstalk Between the Gut Microbiota and Mitochondria During Exercise

Overview
Journal Front Physiol
Date 2017 Jun 6
PMID 28579962
Citations 144
Authors
Affiliations
Soon will be listed here.
Abstract

Many physiological changes occur in response to endurance exercise in order to adapt to the increasing energy needs, mitochondria biogenesis, increased reactive oxygen species (ROS) production and acute inflammatory responses. Mitochondria are organelles within each cell that are crucial for ATP production and are also a major producer of ROS and reactive nitrogen species during intense exercise. Recent evidence shows there is a bidirectional interaction between mitochondria and microbiota. The gut microbiota have been shown to regulate key transcriptional co-activators, transcription factors and enzymes involved in mitochondrial biogenesis such as α, and genes. Furthermore, the gut microbiota and its metabolites, such as short chain fatty acids and secondary bile acids, also contribute to host energy production, ROS modulation and inflammation in the gut by attenuating TNFα- mediated immune responses and inflammasomes such as . On the other hand, mitochondria, particularly mitochondrial ROS production, have a crucial role in regulating the gut microbiota via modulating intestinal barrier function and mucosal immune responses. Recently, it has also been shown that genetic variants within the mitochondrial genome, could affect mitochondrial function and therefore the intestinal microbiota composition and activity. Diet is also known to dramatically modulate the composition of the gut microbiota. Therefore, studies targeting the gut microbiota can be useful for managing mitochondrial related ROS production, pro-inflammatory signals and metabolic limits in endurance athletes.

Citing Articles

Atrial fibrillation risk model based on LASSO and SVM algorithms and immune infiltration of key mitochondrial energy metabolism genes.

Yang X, Lan W, Lin C, Zhu C, Ye Z, Chen Z Sci Rep. 2025; 15(1):6681.

PMID: 39994392 PMC: 11850640. DOI: 10.1038/s41598-025-91047-3.


Role of ferroptosis in atrial fibrillation: a review.

Fan S, Hu Y, Shi J Front Pharmacol. 2025; 16:1362060.

PMID: 39981174 PMC: 11839810. DOI: 10.3389/fphar.2025.1362060.


Nutritional Strategies for Enhancing Performance and Training Adaptation in Weightlifters.

Hwang D, Yang H Int J Mol Sci. 2025; 26(1.

PMID: 39796095 PMC: 11720227. DOI: 10.3390/ijms26010240.


Short-Term Supplementation of Sauerkraut Induces Favorable Changes in the Gut Microbiota of Active Athletes: A Proof-of-Concept Study.

Karacic A, Zonjic J, Stefanov E, Radolovic K, Starcevic A, Renko I Nutrients. 2025; 16(24.

PMID: 39771042 PMC: 11677004. DOI: 10.3390/nu16244421.


Myokines and Microbiota: New Perspectives in the Endocrine Muscle-Gut Axis.

Saponaro F, Bertolini A, Baragatti R, Galfo L, Chiellini G, Saba A Nutrients. 2024; 16(23).

PMID: 39683426 PMC: 11643575. DOI: 10.3390/nu16234032.


References
1.
Gray M, Burger G, Lang B . Mitochondrial evolution. Science. 1999; 283(5407):1476-81. DOI: 10.1126/science.283.5407.1476. View

2.
Wu Z, Puigserver P, Andersson U, Zhang C, Adelmant G, Mootha V . Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1. Cell. 1999; 98(1):115-24. DOI: 10.1016/S0092-8674(00)80611-X. View

3.
Ahmad M, Krishnan S, Ramakrishna B, Mathan M, Pulimood A, Murthy S . Butyrate and glucose metabolism by colonocytes in experimental colitis in mice. Gut. 2000; 46(4):493-9. PMC: 1727901. DOI: 10.1136/gut.46.4.493. View

4.
Kurland C, Andersson S . Origin and evolution of the mitochondrial proteome. Microbiol Mol Biol Rev. 2000; 64(4):786-820. PMC: 99014. DOI: 10.1128/MMBR.64.4.786-820.2000. View

5.
Hood D . Invited Review: contractile activity-induced mitochondrial biogenesis in skeletal muscle. J Appl Physiol (1985). 2001; 90(3):1137-57. DOI: 10.1152/jappl.2001.90.3.1137. View