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Melanotan II
Mechanism, Dosing, Effects
Melanotan II is a synthetic analog of α-melanocyte-stimulating hormone (α-MSH). It is primarily studied for its ability to increase skin pigmentation (tanning) and is also known to stimulate libido and erectile activity as secondary effects. It activates melanocortin receptors, leading to melanin production in the skin.
Mechanism of Action
Melanotan II works by:
- Activating MC1R receptors in melanocytes
- Increasing melanin production
- Enhancing UV-independent tanning
- Stimulating MC3R & MC4R receptors (linked to libido & appetite control)
- Increasing cAMP signaling → pigment synthesis
This leads to progressive skin darkening even with minimal sun exposure.
Dosing Strategy
Route: Subcutaneous
Vial: 10 mg
Reconstitution
- Add 3.0 mL bacteriostatic water
- Concentration: 3.33 mg/mL
- Syringe reference:
- 1 unit = 33.3 mcg
Standard Titration Protocol
Loading Phase
Week 1
→ 250 mcg daily
→ 7.5 units (0.075 mL)
Week 2
→ 500 mcg daily
→ 15 units (0.15 mL)
Week 3
→ 750 mcg daily
→ 22.5 units (0.225 mL)
Weeks 4–8
→ 1000 mcg daily
→ 30 units (0.30 mL)
Maintenance Phase
After pigmentation achieved:
→ 500–1000 mcg
→ 1–2× per week
Cycle Length
- Loading: 6–8 weeks
- Maintenance: As needed
Effects and Outcomes
Commonly observed:
- Progressive skin tanning
- Reduced sunburn risk
- Increased libido
- Possible spontaneous erections
- Appetite suppression (mild)
- Freckle darkening
- Long-lasting pigmentation
Safety and Tolerability
Common side effects
- Nausea
- Facial flushing
- Yawning
- Mild fatigue
- Increased libido
Less common
- Temporary darkening of moles/freckles
- Injection-site irritation
Safety Notes
- Start low dose to reduce nausea
- Do NOT exceed recommended dosing
- Rotate injection sites
- Not FDA-approved
- Avoid excessive UV exposure
- Monitor moles for changes
