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Melanotan-1 Be Cycled Like Other Research Compounds: Comparison

Growth Hormone Secretagogues (MK-677, GHRP-2) Suppression of endogenous GH pulsatility; ghrelin receptor desensitisation 8–12 weeks on, 4–8 weeks off No endocrine suppression; no receptor desensitisation MT-1 requires no washout for receptor or hormonal recove

This comparison does not assign a generated winner or score.

  • Growth Hormone Secretagogues (MK-677, GHRP-2)
  • Suppression of endogenous GH pulsatility; ghrelin receptor desensitisation
  • 8–12 weeks on, 4–8 weeks off
  • No endocrine suppression; no receptor desensitisation
  • MT-1 requires no washout for receptor or hormonal recovery
  • Beta-2 Agonists (Clenbuterol, Albuterol)
  • Rapid beta-adrenergic receptor downregulation
  • 2 weeks on, 2 weeks off (or continuous with ketotifen)
  • MC1R remains fully responsive under continuous agonism
  • Standard cycling rationale does not apply to melanocortin receptors
  • SARMs (RAD-140, LGD-4033)
  • HPG axis suppression; potential hepatotoxicity
  • 8–12 weeks on, 4–8 weeks off + PCT
  • No suppression of testosterone or gonadotropins
  • MT-1 has no impact on reproductive hormone axis
  • Melanotan-1 (Afamelanotide)
  • Cumulative melanogenesis; no receptor tolerance
  • Front-load 10–20 days, maintenance or cessation for months
  • Effect persists 45–60 days after stopping
  • Cycling is optional and protocol-dependent, not pharmacologically mandated
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