Low subcutaneous doses of MIF-1 produced significant improvement in patients with major depression in a small trial.
Melanostatin DM (MIF-1)
MIF-1 peptide for mood regulation and dopamine modulation

Overview
Last reviewed: 2026-08-18
Identity & Aliases
Also known as
Full composition (formula, molecular weight, sequence) in Quick Facts →
Research Areas
Available Evidence
Early clinical studies reported improvement in major depression after low subcutaneous doses of MIF-1 (1994, PMID 7989637), while trials in Parkinson's disease showed no behavioral benefit over L-dopa (1979, PMID 39308). Overall human evidence is old, small, and mixed.
Rodent studies show MIF-1/PLG and its peptidomimetic PAOPA attenuate haloperidol-induced vacuous chewing movements (a tardive-dyskinesia model) and modulate dopamine and opioid systems.
The '-DM' suffix in the product name (melanostatin-dm) does not correspond to a standard published designation; many modern claims about mood/neuroprotection extrapolate from dated 1970s-1990s literature and lack contemporary replication.
Key Studies & Findings
MIF-I failed to affect behavioral responses in patients with Parkinson's disease under L-dopa therapy.
PLG and peptidomimetic PAOPA attenuated haloperidol-induced vacuous chewing movements in rats, a model of human tardive dyskinesia.
Benefits & Effects
Side Effects & Safety
Limitations & Open Questions
Pharmacology
Reported Research Dosing
Reported values from research literature and community protocols. Educational reference only — not a dosing recommendation or medical advice.
dosage not established
Frequently Asked Questions
What is the 'DM' in melanostatin-dm?
No standard published definition was found; it appears to be a vendor/product-specific designation, and the underlying compound literature refers to MIF-1 (Pro-Leu-Gly-NH2).
Is there modern evidence for melanostatin in depression?
The positive human signal dates to a 1994 small trial; no contemporary large or replicated trials support current use.
Related Resources
Quick Facts
Formula
C13H24N4O3
Molecular Weight
284.0
Sequence
PLG
Mechanism
Dopamine modulator for mood regulation and cognitive enhancement
Safety Information
Research compound. Limited human data. D2 receptor allosteric modulator.