Humanin vs MOTS-c

Mitochondrial-derived peptide vs Mitochondrial-derived peptide · Head-to-head comparison

Two peptides encoded in mitochondrial DNA rather than the nuclear genome, and the two compounds on this site with the most similar evidence profile: real human observational data about endogenous levels, and nothing at all about administering them.

Side by side

 HumaninMOTS-c
ClassMitochondrial-derived peptideMitochondrial-derived peptide
StatusResearch compoundResearch compound
RouteSubcutaneous injectionSubcutaneous injection
Typical vials10 mg5 mg, 10 mg
Dose range1 mg to 2 mg5 mg to 10 mg
FrequencyDaily or a few times weeklyWeekly, often split
Half-lifeNo human dataNo human data
Dosing unitmilligramsmilligrams

Pharmacokinetics

No curves are shown, on purpose.

No published human pharmacokinetics for Humanin or MOTS-c. Drawing one curve against an absent one would imply a comparison that cannot be made.

What the evidence supports

These grade how well each outcome has been studied in humans, never how well either compound works. A strong grade can sit on a negative result.

Both top out at the same tier of evidence: Human, observational. Where they differ is in which outcomes have been asked about, not in how well either has been studied overall.

Humanin

OutcomeEvidence
Endogenous levels decline with ageHuman, observational
NeuroprotectionAnimal only
Cytoprotective signalingMechanistic only
Any outcome from administration in humansNo data

MOTS-c

OutcomeEvidence
Endogenous levels correlate with fitnessHuman, observational
Exercise capacityAnimal only
Metabolic homeostasisAnimal only
Any outcome from administration in humansNo data
Human, observationalReported in people without randomization: open-label, single-arm, retrospective, or case series.
Animal onlyShown in animals. No published human trial reports it.
Mechanistic onlySupported only by cell, tissue or biochemical work, or by reasoning from a related molecule.
No dataNo published evidence at any level that we could find.

How to choose

The distinction that matters is endogenous versus administered

Both have human data showing levels decline with age or associate with outcomes. Neither has a trial of anyone being dosed.

Humanin is cytoprotective, MOTS-c is metabolic

Humanin binds IGFBP-3 and formyl peptide receptors and was found in neurons surviving Alzheimer-affected tissue. MOTS-c acts on AMPK.

Observational levels are not a dosing rationale

That a molecule declines with age does not establish that supplying more of it helps, which is the untested step in both.

At the syringe

At the default setup on each compound's own page, a 10 mg vial in 2 mL puts 50 mcg on every insulin unit, while a 10 mg vial in 2 mL puts 50 mcg on every unit. That is the number that decides whether a dose lands on a readable mark, and it is set by how much water goes in, not by the compound.

Full references