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Abstract
Bile acids may orchestrate a regulatory network affecting mitochondrial quality control through several receptors.
- Bile acids regulate mitochondrial biogenesis, dynamic equilibrium, selective autophagy, and redox balance.
- TGR5 activates mitochondrial biogenesis through a specific signaling pathway while also influencing mitochondrial fission and calcium levels.
- FXR is involved in regulating fatty acid breakdown, antioxidant defense, and cell death pathways, and can improve certain autophagy processes in liver disease.
- Other receptors like S1PR2, VDR, and PXR also contribute to the regulation of mitochondrial function and autophagy.
- Dysregulation of this network is linked to various metabolic disorders, including fatty liver disease and diabetic complications.
- Agonists targeting these receptors have shown potential in restoring mitochondrial function and reducing tissue damage in animal studies.
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