Table 1.
Therapeutic intervention for mitochondria in different liver models.
| Therapeutics | Models | Main effects | Route of administration | Reference |
|---|---|---|---|---|
| Cilostazol | Ischemia-reperfusion injury | Increases PGC-1α expression and mtDNA content | Oral | 134 |
| Coenzyme Q10 | Liver fibrosis | Enhances autophagy | Oral | 143 |
| Idebenone | Nonalcoholic steatohepatitis | Regulates lipid metabolism | Oral | 133 |
| Quercetin | Alcoholic liver disease, acute liver injury | Scavenges mitochondrial reactive oxygen species; increases the anti-apoptotic and anti-inflammatory potential | Oral | 135,144 |
| MitoQ | Hepatitis B virus | Decreases superoxide formation, restores immune function | Oral | 111 |
| Vitamin E | Nonalcoholic fatty liver disease | Reduces reactive oxygen species and alanine transaminase | Oral | 136 |
| Icaritin, dehydrocrenatidine, dichloroacetate | Hepatocellular carcinoma | Enhances mitophagy; recovers Δψm; inhibits mTOR complex 1; suppresses tumor growth | Oral | 137,138,144 |
| Mitochondria | Drug-induced liver injury | Reduces oxidative stress and apoptosis | Spleen injection | 140 |
| Mesenchymal stroma cells-extracellular vesicles | Nonalcoholic fatty liver disease, ischemia-reperfusion injury | Increases mitochondrial respiratory chain activity and adenosine triphosphate production | Injection | 141,142 |