Hexarelin dose-dependently increased GH secretion in healthy humans.
Hexarelin
Potent growth hormone releasing peptide with cardioprotective effects

🛑 WADA BANNED - Prohibited in competitive sports as potent growth hormone releasing agent
Overview
Last reviewed: 2026-08-18
Identity & Aliases
Also known as
Status: Research compound - Growth hormone agonist
Full composition (formula, molecular weight, sequence) in Quick Facts →
Research Areas
Available Evidence
Clinical studies show hexarelin stimulates GH release in a dose-dependent manner in healthy subjects, including via intranasal and oral routes without short-term desensitization, and its blunted GH response in elderly subjects can be restored by arginine/GHRH priming. Cardiotropic studies reported GH-independent improvements in cardiac function measures in patients with dilated or ischemic cardiomyopathy.
Rodent studies identified CD36 as the cardiac binding site mediating GH-independent cardiovascular actions of growth hormone-releasing peptides such as hexarelin, supporting direct cardioprotective effects beyond GH release.
Hexarelin acts as an agonist at the ghrelin receptor GHS-R1a, and laboratory assays demonstrate CD36 binding in cardiac tissue.
Clinical evidence is largely from small, short-term studies from the 1990s-2000s; long-term efficacy for muscle, aging, or cardiac outcomes is unproven, and there is no approved indication.
Key Studies & Findings
GH-independent cardiotropic activity of hexarelin observed in normal subjects, GH-deficient patients, and patients with idiopathic or ischemic dilated cardiomyopathy.
Hexarelin improved cardiac function measures in patients with severe left ventricular dysfunction due to dilated or ischemic cardiomyopathy.
CD36 identified as the cardiac receptor site mediating the cardiovascular action of growth hormone-releasing peptides including hexarelin.
Benefits & Effects
Cardioprotective effects via cardiac CD36 receptor
Improved cardiac function post-myocardial infarction
Reduced visceral fat and liver triglycerides
Improved insulin sensitivity
Side Effects & Safety
Appetite increase
ACTH/cortisol stimulation
Blood glucose effects
Mild-Moderate side effect
Onset: Hours
Management: Monitor; more pronounced than other GHRPs
Dose-dependent
Limitations & Open Questions
Pharmacology
Reported Research Dosing
Reported values from research literature and community protocols. Educational reference only — not a dosing recommendation or medical advice.
100-300 mcg 2-3x/day
Research Protocols
GH Optimization
- Dose
- 100 mcg
- Frequency
- 3x daily (morning, midday, evening)
- Route
- SubQ
Cardioprotection Research
- Dose
- 100-200 mcg
- Frequency
- 2x daily
- Route
- SubQ
Recovery/Anti-Aging
- Dose
- 100 mcg
- Frequency
- 2x daily (morning and bedtime)
- Route
- SubQ
With GHRH (Synergistic)
- Dose
- 100 mcg hexarelin + 100 mcg CJC-1295
- Frequency
- 2-3x daily
- Route
- SubQ
Research protocols are for educational purposes only. Always consult qualified medical professionals.
Frequently Asked Questions
Is hexarelin approved for medical use?
No. It has been studied clinically for GH stimulation and cardiac function but has no approved indication and is sold only as a research compound.
How does hexarelin differ from GHRH or GH itself?
Hexarelin stimulates the ghrelin (GHS-R1a) pathway rather than the GHRH receptor, and it also has GH-independent effects such as direct cardiac actions.
Research Citations
Massoud AF, Hindmarsh PC, Brook CG (1997)
Mao Y, Tokudome T, Kishimoto I (2014)
Guan C, Li C, Shen X, Yang C, Liu Z, Zhang N, Xu L, Zhao L, Zhou B, Man X, Luo C, Luan H, Che L, Wang Y, Xu Y (2023)
Jiang B, Wang M, Li X, Ren P, Li G, Wang Y, Wang L, Li X, Yang D, Qin L, Xin S (2022)
+ 21 more citations
Related Resources
Quick Facts
Formula
C47H58N12O6
Molecular Weight
887.04
Sequence
His-D-2MeTrp-Ala-Trp-D-Phe-Lys-NH2
Mechanism
Synthetic hexapeptide with strong GH-releasing activity
Safety Information
Research compound only. Limited human safety data available.
Citations
26Massoud AF, Hindmarsh PC, Brook CG (1997)
Mao Y, Tokudome T, Kishimoto I (2014)
Guan C, Li C, Shen X, Yang C, Liu Z, Zhang N, Xu L, Zhao L, Zhou B, Man X, Luo C, Luan H, Che L, Wang Y, Xu Y (2023)
Jiang B, Wang M, Li X, Ren P, Li G, Wang Y, Wang L, Li X, Yang D, Qin L, Xin S (2022)
+ 21 more citations