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MOTS-c Studied Insulin Resistance Research: Comparison Table

USC 2015 (Cell Metabolism) High-fat diet mice 15 mg/kg IP, 12 weeks 27% weight reduction, fasting glucose 215→142 mg/dL AMPK activation via DHFR binding Established foundational mechanism. Direct metabolic benefit in diet-induced obesity model Singapore Genera

This comparison does not assign a generated winner or score.

  • USC 2015 (Cell Metabolism)
  • High-fat diet mice
  • 15 mg/kg IP, 12 weeks
  • 27% weight reduction, fasting glucose 215→142 mg/dL
  • AMPK activation via DHFR binding
  • Established foundational mechanism. Direct metabolic benefit in diet-induced obesity model
  • Singapore General 2021
  • Human Phase I (n=24)
  • 5–20 mg SC 3×/week, 4 weeks
  • Fasting glucose −14 mg/dL, fasting insulin −11% at 15 mg
  • Not mechanistically assessed in trial
  • Demonstrated human safety and preliminary glycemic efficacy signal
  • Tohoku 2023
  • Human exercise trial (n=36)
  • 10 mg SC pre-exercise, single dose
  • Lactate −19%, glucose clearance 23 min faster
  • Improved mitochondrial oxidative capacity
  • Showed acute metabolic benefit during physical stress. Suggests performance application beyond glucose control
  • Alabama 2025
  • Prediabetic adults (n=48)
  • 15 mg SC 3×/week, 12 weeks
  • HbA1c 6.1%→5.8%, HOMA-IR −28%, fat loss with lean mass preservation
  • Not mechanistically characterized
  • Longest human trial to date. HbA1c shift clinically meaningful for prediabetes reversal trajectory
  • Korean metabolic study 2024
  • Type 2 diabetic mice
  • 10 mg/kg IP daily, 8 weeks
  • Hepatic glucose production −34%, muscle glucose uptake +41%
  • Suppression of G6Pase and PEPCK gene expression in liver
  • Demonstrated dual action. Both reduced hepatic output and increased peripheral uptake
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