Mitochondrial Optimization Protocol (MOTS-c + SS-31)
Restore mitochondrial biogenesis, improve cellular energy production, reduce oxidative damage, and address age-related metabolic decline through targeted mitochondrial peptides.
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This protocol is an educational example only. It does not apply to your specific health situation. Medical supervision is required. Peptide therapy is not approved by regulatory bodies for many of the described indications.
Protocol Stack
MOTS-c
PrimaryDose
5 mg
Frequency
3Γ per week
Timing
30β60 min before exercise or morning on non-training days
Duration
12 weeks, then 4-week off-cycle
SS-31 (Elamipretide)
PrimaryDose
2 mg
Frequency
Daily
Timing
Morning SC injection
Duration
12 weeks continuous
Humanin
SupportingDose
2 mg
Frequency
3Γ per week
Timing
Evening, alternating days with MOTS-c
Duration
12 weeks, then assess
CoQ10 (adjunct supplement)
OptionalDose
400 mg
Frequency
Daily
Timing
With largest meal
Duration
Ongoing
Monitoring Parameters
- βBaseline: fasting glucose, HbA1c, lactate, VO2max or 6-minute walk test, subjective fatigue score (VAS)
- βWeek 6: repeat fasting glucose, HbA1c, subjective fatigue reassessment
- βWeek 12: full repeat panel + VO2max/6MWT, consider GrimAge methylation clock if available
- βOngoing: resting heart rate (indicator of mitochondrial efficiency), sleep quality tracking
- βSafety: liver enzymes (ALT/AST) at baseline and week 6 β MOTS-c influences hepatic metabolism
Expected Outcomes
Weeks 1β3: improved sleep quality and morning energy; reduced post-exercise recovery time
Weeks 4β6: measurable reduction in fasting glucose (typically 5β12%); subjective fatigue score improvement β₯30%
Weeks 8β12: improved exercise tolerance (VO2max or 6MWT); body composition changes (reduced visceral fat without caloric restriction)
Post-cycle: effects of SS-31 on cardiac and mitochondrial function persist beyond the active protocol
Contraindications
- βInsulin-dependent diabetes β MOTS-c activates GLUT4/AMPK; hypoglycaemia risk requiring close glucose monitoring
- βActive cardiac arrhythmia β SS-31 influences mitochondrial membrane dynamics; cardiac clearance advised
- βPregnancy and breastfeeding
- βCurrent treatment with immunosuppressants β Humanin modulates apoptotic pathways
Clinical Notes
This is a research-grade protocol β MOTS-c and Humanin have no established human clinical dosing guidelines; SS-31 has Phase 2 human data in cardiac settings. All three are available only as research peptides. Introduce sequentially: start SS-31 alone week 1β2, add MOTS-c week 3, add Humanin week 5 if well tolerated. This staged introduction allows attribution of any side effects to individual agents. Compounding quality is critical β request COA for each batch.
Case Study
Clinical Practice Example
Male, 52, endurance athlete (marathon runner), presenting with progressive exercise intolerance, elevated resting lactate (2.4 mmol/L), and HbA1c creeping to 5.8%. VO2max measured at 44 ml/kg/min β low for his training volume. Started protocol with SS-31 2 mg daily + MOTS-c 5 mg 3Γ/week before training. Humanin added at week 5. Week 12 results: resting lactate normalised to 1.1 mmol/L, HbA1c 5.4%, VO2max improved to 51 ml/kg/min. Subjective recovery time between training sessions reduced from ~72h to ~36h. No adverse events.