GHRP-6 (10 mg Vial) Dosage Protocol

Educational resource for reconstitution and administration of GHRP-6, a synthetic hexapeptide investigated for its capacity to trigger pulsatile growth hormone secretion via ghrelin receptor activation and support anabolic outcomes through IGF-1 elevation.

Quickstart Highlights

GHRP-6 represents a synthetic hexapeptide that operates as a robust growth hormone secretagogue through its binding to the ghrelin receptor (GHS-R1a). This mechanism initiates pulsatile GH discharge from the pituitary gland while preserving natural feedback regulation, boosting IGF-1 concentrations and facilitating anabolic advantages via a thrice-daily subcutaneous regimen.

  • Reconstitute: Add 3.0 mL bacteriostatic water to yield approximately 3.33 mg/mL concentration
  • Standard range: 100–300 mcg per dose, administered three times daily (subcutaneous)
  • Easy measuring: At 3.33 mg/mL, 1 unit = 0.01 mL = 33.3 mcg on a U-100 insulin syringe
  • Storage: Lyophilized powder: freeze at −20 °C (−4 °F); reconstituted solution: refrigerate at 2–8 °C (35.6–46.4 °F) and consume within 7 days

Dosing & Reconstitution Guide

Educational reference for reconstitution procedures and daily administration

Subcutaneous Protocol (3 mL = ~3.33 mg/mL)

Week/Phase Dose per Injection Units (per injection) mL
Weeks 1–2 100 mcg 3 units 0.03 mL
Weeks 3–4 200 mcg 6 units 0.06 mL
Weeks 5–12 300 mcg 9 units 0.09 mL

Frequency: Three times daily subcutaneously, spaced at least 4 hours apart (morning, midday, bedtime). On empty stomach (2–3 hours after meals, 30 minutes before eating).

Reconstitution Steps

  1. Draw 3.0 mL bacteriostatic water with sterile syringe
  2. Inject slowly down vial wall to avoid foaming; do not shake
  3. Gently swirl or roll until powder completely dissolves
  4. Label with date and concentration; refrigerate at 2–8 °C (35.6–46.4 °F), protected from light
  5. Use within 7 days of reconstitution for optimal potency

How This Works

GHRP-6 operates as a synthetic ghrelin mimetic through its binding affinity to the growth hormone secretagogue receptor (GHS-R1a) located in both pituitary and hypothalamic tissues. This interaction precipitates acute pulsatile GH discharge while simultaneously diminishing somatostatin's suppressive influence. Unlike continuous GH administration, GHRP-6 upholds physiological feedback mechanisms—as GH and IGF-1 concentrations increase, endogenous somatostatin production rises to prevent excessive elevation, maintaining pulses within normal physiological boundaries.

Furthermore, GHRP-6 demonstrates cytoprotective characteristics through engagement with the CD36 receptor present on immune and muscle cells, triggering cell-survival signaling cascades (PI3K/Akt) that shield tissues from oxidative damage and inflammatory processes.

Potential Benefits & Side Effects

Observations derived from preclinical and early clinical research literature.

Potential Benefits

Potential Side Effects

Injection Technique

General subcutaneous administration guidance based on clinical best-practice protocols.

Important Notes

Practical considerations for consistency and safety protocols.

Storage Instructions

Supplies Needed (12-Week Protocol)

Item Quantity
GHRP-6 vials (10 mg each) ~7 vials
Insulin syringes (U-100) 252 syringes (3 × 100-count boxes)
Bacteriostatic water (10 mL bottles) 3 bottles (~21 mL total)
Alcohol swabs 504 swabs (6 × 100-count boxes)

Important Disclaimer: This content is intended for educational purposes only and does not constitute medical advice, diagnosis, or treatment. GHRP-6 is intended for research purposes only. Always consult with a qualified healthcare professional before starting any new research protocol.

References

European Journal of Endocrinology
GHRP mechanisms and pulsatile GH secretion
Clinical Medicine Insights: Cardiology
Cytoprotective effects and CD36 receptor signaling
European Journal of Pharmaceutical Sciences
Pharmacokinetics and ~2.5 hour half-life