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. Author manuscript; available in PMC: 2020 Apr 1.
Published in final edited form as: J Mol Med (Berl). 2019 Feb 20;97(4):487–490. doi: 10.1007/s00109-019-01758-0

Table 1.

MOTS-c alleviates various pathological conditions

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]