GHRP-6: Growth Hormone-Releasing Peptide-6

First-generation synthetic hexapeptide ghrelin mimetic. Induces strong hunger alongside GH release. Not an approved medicine.

👥 Human studies

Full name
GHRP-6 (His-D-Trp-Ala-Trp-D-Phe-Lys-NH2)
Class
Ghrelin receptor (GHS-R) agonist — peptide
Half-life
~15–30 minutes
Route
Subcutaneous, intranasal
Developer
Academic (Bowers, 1980s)
Regulatory status
No approval; WADA-banned

What it is

GHRP-6 was the original synthetic ghrelin receptor agonist developed by Cyril Bowers in the 1980s — before endogenous ghrelin was identified. It activates the same receptor and produces a GH pulse, but also strongly stimulates appetite via hypothalamic ghrelin-receptor activation.

How it works

GHS-R1a activation on pituitary somatotrophs drives GH secretion. Parallel activation of hypothalamic neuron populations (particularly arcuate NPY/AgRP) increases hunger — a more prominent effect than with GHRP-2.

Like GHRP-2, GHRP-6 raises prolactin and ACTH/cortisol modestly. Effects synergise with GHRH.

What the research shows

Historical pharmacodynamic studies underpin more modern GH secretagogue programmes.

Bowers CY et al. (1984) — first human GHRP-6 study

Bowers C.Y. et al., Endocrinology 1984;114:1537–1545 (rodent/translational); J Clin Endocrinol Metab 1990;70:975–982 (human). 👥🐀 Human + animal

Acute GHRP-6 IV produced clear dose-dependent GH pulses in healthy adults.

This class of compound validated that non-GHRH, non-somatostatin mechanisms regulate GH secretion — leading decades later to ghrelin discovery.

Limitations: Historical; no long-term data for therapeutic use.

Laferrère B. et al. (2005) — appetite effect

Laferrère B. et al., J Clin Endocrinol Metab 2005;90:611–614. 👥 Human studies

Acute GHRP-6 infusion in healthy adults significantly increased food intake at a subsequent meal.

This orexigenic effect is the most consistent non-GH action and distinguishes GHRP-6 from GHRP-2 and ipamorelin.

Limitations: Acute, not chronic; small cohort.

Safety and limitations

Acute effects well tolerated: flushing, hunger, mild cortisol/prolactin rises. Chronic safety is not established.

Peptides sold in unregulated markets labelled “GHRP-6” vary widely in purity. WADA-banned.

Sources

  1. Bowers C.Y. et al. J Clin Endocrinol Metab 1990;70:975–982. PubMed
  2. Laferrère B. et al. J Clin Endocrinol Metab 2005;90:611–614. PubMed

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