MIF-1

Also known as: Melanocyte-Inhibiting Factor; Pro-Leu-Gly-NH2; Melanostatin

Overview

MIF-1 is an endogenous tripeptide neuromodulator that crosses the BBB and modulates dopamine receptors and neuropeptide release. It shows antidepressant, nootropic, and anti-Parkinsonian effects with rapid onset and minimal side effects in studies.

Benefits

- Antidepressant effects

- Cognitive enhancement

- Motor control support

- Addiction support

Consider This Peptide If You Want To

- Support mood regulation and mental well-being

- Enhance cognitive function and neuroprotection

Dosage & Administration

Dosage Guidelines

Recommended Dosage

• Amount:5 mg

• Frequency:weekdays

• Duration:1 week

• Rest Period:1 week

• Time of Day:morning

• Ingestion:subcutaneous

Administration Routes:SubcutaneousOral

Oral Administration:

• Standard Dosage: 60-75 mg daily

• Timing:

• Duration:

Research Findings on Dosage:

• Subcutaneous Injection:

◦ Commonly Reported Dosage: 10 mg once daily

◦ Duration: 5 days. Repeat cycles after a 1--2-week interval as needed.

• Oral Administration:

◦ Commonly Reported Dosage: 60--75 mg daily, divided into smaller doses or taken once per day.

Mechanism of Action

Mechanism of Action

How this peptide works in the body

Dopamine Receptor Modulation:

Acts as a positive allosteric modulator for D2 and D4 dopamine receptors, increasing their responsiveness to dopamine. This interaction stabilizes neurotransmission, promoting mood enhancement and cognitive function by increasing cAMP signaling and reducing excitotoxicity.

Opioid Receptor Interaction:

Inhibits opioid receptor activation by reducing receptor binding affinity for endogenous opioids, contributing to its anti-addictive and mood-regulating properties. This action involves interference with the G-protein coupled receptor pathways.

Inhibition of Alpha-MSH Release:

Modulates the hypothalamic-pituitary axis by decreasing melanocyte-stimulating hormone secretion, thus impacting neuropeptide balance and influencing stress and mood responses. The reduction occurs via direct inhibition of prohormone convertase enzymes.

Neurotransmitter Regulation:

Enhances norepinephrine and dopamine levels in specific brain regions such as the striatum and cortex, influencing mood and motivation. This regulation is achieved through altered reuptake transporter dynamics and enzyme inhibition, including monoamine oxidase.

Consider Stacking With

- Cerebrolysin (nootropic peptides)

- Anti-inflammatory agents

- Dopamine agonists

Side Effects & Cautions

Common Side Effects

- Generally well-tolerated; rare mild GI discomfort or headache

Cautions

- Avoid concurrent use with opioid medications (may negate effects)

Rare Side Effects

- Unusual sensitivity reactions in atypical peptide metabolism

Research & References

Research Highlights

Antidepressant Activity: Clinical trials demonstrate rapid and sustained relief from depressive symptoms, outperforming standard treatments like SSRIs in initial response times.

Cognitive Enhancement: Preclinical studies reveal improved spatial learning and memory retention in rodent models.

Neuroprotection: Research shows reduced neuroinflammation and protection against ischemic brain injury.

References

Kastin, A. J., et al., "Clinical Implications of MIF-1 in Depression Treatment," Journal of Neuroendocrinology, 1980

Bloom, J., "MIF-1 as a Dopaminergic Modulator: Applications in Neuropsychiatry," Neuroscience Reviews, 2014

Smith, R. et al., "Mechanistic Insights into MIF-1 Neuroprotection," Peptide Science Advances, 2023

Nycomed Data, "Therapeutic Peptides: MIF-1 and Beyond," 2022

Sundberg, P., "MIF-1 in Opioid Receptor Modulation," International Journal of Neuropharmacology, 2023