Peptides

Sermorelin

Evidence: strong_human

Mechanism of Action

Sermorelin is a synthetic 29-amino acid peptide representing the biologically active fragment of GHRH (amino acids 1-29) with full functional activity. It activates GHRH receptors on pituitary somatotrophs, stimulating cAMP production via Gs protein/adenylate cyclase and MAP kinase pathways. Due to the interactive effects of sermorelin and endogenous somatostatin, GH release is episodic rather than continuous. Sermorelin also stimulates pituitary gene transcription of GH mRNA, increasing and preserving pituitary GH reserve.

Dosing Protocol

Standard: Research indicates 200-300 mcg administered once daily at bedtime via subcutaneous injection.

Maintenance: Research indicates 100-200 mcg at bedtime for maintenance.

Administration: subcutaneous

Timing: Bedtime administration (aligns with natural nocturnal GH release). On empty stomach.

Duration: 12-24 week cycles. Some protocols use continuous treatment.

Notes

Sermorelin was FDA-approved in 1997 for pediatric GH deficiency diagnosis and treatment, giving it one of the strongest safety profiles in the GHRH category. Discontinued in 2008 due to manufacturing issues (not safety). Short half-life (11-12 minutes) means it produces physiological GH pulses. Commonly considered the safest entry point for GH optimization. Stacking with a GHRP (Ipamorelin preferred) provides synergistic amplification of GH release.

Stacking

  • Ipamorelin
  • GHRP-2
  • GHRP-6

Interactions

  • Insulin [HIGH] — GH elevation antagonizes insulin sensitivity.
  • Glucocorticoids [MEDIUM] — May blunt GH response.
  • Thyroid hormones [LOW] — Hypothyroidism reduces GH response to sermorelin; ensure thyroid is optimized.

Contraindications

  • Active cancer
  • Pregnancy and breastfeeding
  • Intracranial hypertension

Side Effects

  • Injection site reactions
  • Facial flushing
  • Headache
  • Dizziness
  • Transient taste changes

Key Papers

  • 10.2165/00003495-200767180-00005
  • 10.1177/1557988317718662

Source Quality

Compounding pharmacy (503A/503B). Was previously FDA-approved (1997) but discontinued in 2008 due to manufacturing difficulties, not safety concerns.

Disclaimer: This information is for educational purposes only and is not medical advice. BioAccelera Labs does not diagnose, treat, or prescribe. Consult a licensed healthcare provider before using any compound.

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