MOTS-c
Mitochondrial open reading frame of 12S rRNA, type c
MOTS-c activates AMPK through an AICAR-independent pathway and modulates the endothelin A receptor, ETAR. It improves coupling of mitochondrial energy processes. Movement into the nucleus allows it to influence expression of genes involved in responses to stress.
Not medical advice. Educational reference only.
- Typical dose
- Injectable research (route unspecified): 5–10 mg weekly
- Route
- Subcutaneous injection (administration guidance); injectable, route unspecified (5–10 mg weekly research range)
- Storage
- Keep at 2–8°C after mixing and use within 28 days.
What is MOTS-c?
MOTS-c contains 16 amino acids and belongs to the mitochondria-derived peptide family. Its coding region lies within mitochondrial 12S rRNA, making it one of the small number of proteins encoded by mitochondrial DNA. Animal experiments and early human investigations link it to AMPK activation, better insulin sensitivity, increased exercise capacity and less metabolic deterioration with age. It remains a research compound.
Research schedules name a low starting amount and a titrated standard amount without numeric doses. Frequency depends on the protocol, and the route varies.
Responses differ between individuals. Begin with the lowest dose and observe your response carefully. Speak with your clinician before use and report unexpected symptoms. Human adverse effects are not fully characterized for every compound.
Mechanism of action
MOTS-c activates AMPK through an AICAR-independent pathway and modulates the endothelin A receptor, ETAR. It improves coupling of mitochondrial energy processes. Movement into the nucleus allows it to influence expression of genes involved in responses to stress.
Targets: AMPK · ETAR (endothelin A receptor)
Research indications
Energy Metabolism
EffectiveInvestigations indicate improved mitochondrial energy handling and production of ATP.
Metabolic Health
EffectivePotential metabolic effects include increased insulin sensitivity and better glucose handling.
Longevity Markers
ModeratePreliminary work indicates possible changes in markers associated with cellular aging.
Interactions
Medications
CautionAsk your prescriber to review any medication before combining treatments.
BPC-157
CompatibleNAD+
CompatibleVitamin D
Compatible
How to reconstitute and inject
Diluent: Use bacteriostatic water; avoid saline because precipitation may occur.
- Let the refrigerated vial stand at room temperature for 15–20 minutes before preparation.
- Disinfect the stopper using an alcohol swab, then wait until it has dried fully in the air.
- Measure the calculated quantity of bacteriostatic water with a sterile syringe. Use only this diluent; avoid saline because precipitation may occur.
- Add the water gradually against the inner vial wall. Keep the stream away from the powder itself.
- Rotate the vial with a gentle swirling motion. Do not shake forcefully, because this can degrade the contents.
- Wait 2–3 minutes for the powder to dissolve completely, and check that the liquid is transparent and has no color.
- Use an insulin syringe to withdraw the calculated amount for injection beneath the skin.
- Inject in the thigh, abdomen or upper arm. Change the injection location each time to help prevent lipodystrophy.
- Refrigerate the mixed solution at 2–8°C. Use it within a maximum of 28 days after preparation.
What to expect
- Week 1–2
- During the first 1–2 weeks, early effects may accompany an adjustment period. Watch for adverse reactions.
- Week 2–4
- By weeks 2–4, the main effects may start becoming apparent. Make dose changes only according to your clinician’s guidance.
- Week 4–8
- During weeks 4–8, the principal effects are expected to be established. Review your progress with your clinician.
- Week 8+
- From week 8 onward, review the results and decide with your clinician whether to continue, cycle or change the dose.
Side effects and safety
- Mild pain, bruising or redness around the injection location
- Possible allergic reaction; stop use if hives or a rash develops
MOTS-c: not approved in the US.
Regulatory status
US
Not approvedFDA: no approval for human treatment; research use only. No 503A ban is identified; compounding authorization remains unknown. Telehealth is available.
- Rx required
- No
- Telehealth
- Available
Frequently asked questions
What is MOTS-c?
This mitochondria-derived peptide participates in metabolic signaling. Early human work and animal studies examine insulin sensitivity, exercise performance and aging-related metabolic change, without establishing an approved therapy.
Which benefits are being investigated?
Investigations indicate improved mitochondrial energy handling and production of ATP. Potential metabolic effects include increased insulin sensitivity and better glucose handling. Preliminary work indicates possible changes in markers associated with cellular aging. Evidence strength differs by outcome; these areas of investigation do not guarantee benefit for an individual.
Which dosing schedules are discussed?
Injectable research discussions include 5–10 mg weekly. The estimated half-life for injectable administration is around 1 hour. These figures do not establish a human treatment regimen.
What safety issues matter?
Adverse effects vary with dose, administration route and individual response. Injection reactions may occur. Discuss unusual symptoms and any proposed combination of medications with your clinician before continuing.
References
The mitochondrial-derived peptide MOTS-c promotes metabolic homeostasis and reduces obesity and insulin resistance. (2015)
MOTS-c: A mitochondrial-encoded peptide regulating muscle function (2021)
MOTS-c improves insulin sensitivity in mice and humans (2019)
MOTS-c: A promising mitochondrial-derived peptide for therapeutic exploitation. (2023)
MOTS-c: A novel mitochondrial-derived peptide regulating muscle and fat metabolism. (2016)
MOTS-c metabolic studies on ClinicalTrials.gov (2024)