Table 1.
Pathological conditions | MOTS-c action | References |
---|---|---|
Aging-associated insulin resistance | Increases glucose uptake in skeletal muscles in aged mice. | [1] |
High-fat diet (HFD)-insulin resistance | Increases insulin sensitivity in HFD-fed mice. Increases GLUT-4 expression in skeletal muscle in HFD-fed mice. |
[1] |
Obesity-associated insulin resistance | Plasma MOTS-c levels are lower in obese male children and adolescents and negatively correlated with markers of insulin resistance and obesity. | [22, 23] |
Nonalcoholic steatohepatitis | Decreases hepatic fat accumulation in HFD-fed mice. MOTS-c analogues prevent NASH in a STAM model |
[1,19] |
Endothelial dysfunction | Improves endothelial function in rats. Plasma MOTS-c levels are lower in human subjects with impaired coronary endothelial function. | [24] |
Menopause-associated conditions | Prevents ovariectomy-induced obesity and insulin resistance. Alleviates ovariectomy-induced osteoporosis. |
[3, 20] |
Osteoporosis/Osteopenia | Alleviates bone loss in ovariectomy-induced osteoporosis via AMPK. Promotes rat bone mesenchymal stem cells differentiation to osteoblasts via TGF-β pathway. |
[20, 21] |
Sepsis | Improves survival in mice during MRSA infection. Enhances bactericidal capacity of macrophages in MRSA-infected mice. | [34] |