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Insulin Action: Conclusions from a 2015 paper noted that MOTS-c has "physiological similarities to the first-line diabetes drug Metformin" with regard to managing glucose utilization, metabolism, and body weight

Under conditions of excessive NAPQI formation or an approximate 70% reduction in glutathione stores, NAPQI covalently binds to the cysteinyl sulfhydryl groups of hepatocellular proteins, forming NAPQI-protein adducts

241 Parallel resistance mechanisms are increasingly attributed to mitophagy-mediated mitochondrial preservation and metabolic resilience, reinforcing the therapeutic relevance of targeting these pathways

None of these agents altered the end-point increase of [Ca 2+ ] i measured in response to JWU-A021 (data not shown)