Review examining MOTS-c as the primary mitochondrial-derived peptide responsible for exercise-induced mitohormesis—covering its induction by mitochondrial stress during exercise, nuclear translocation, AICAR-AMPK pathway activation, and role in mediating the metabolic adaptations to physical activity through mitohormetic mechanisms that explain exercise's beneficial effects on metabolic health. Positions MOTS-c within exercise physiology and mitohormesis. Establishes MOTS-c as the key molecular mediator linking exercise-induced mitochondrial stress to systemic metabolic benefit—providing the theoretical basis for MOTS-c as an exercise mimetic and explaining why MOTS-c supplementation could replicate the metabolic adaptations that require sustained physical activity.
Yoon, Tae Kwan; Lee, Chan Hee; Kwon, Obin; Kim, Min-Seon