At a glance
- Mechanism of action
- GHRP-2 acts as a synthetic agonist at the ghrelin receptor (GHS-R1a) in the anterior pituitary and hypothalamus, inducing a pulsatile GH surge via cAMP/PKC signaling while suppressing somatostatin tone; it also mildly elevates ACTH, cortisol and prolactin.
- Benefits & use
- Acutely increases GH secretion, dose-dependently raises appetite (ghrelin-like) and is used clinically as a diagnostic GH-stimulation test; off-label research interest centers on body composition, sleep quality and recovery.
- Study status
- Several human RCTs exist (Laferrère 2005/2006 on appetite, Haruta 2015 intranasal in anorexia, Veldhuis 2007 on GH-pulse waveform), the foundational work of Bowers on the GHRP class, plus Phase III diagnostic data that supported PMDA approval of pralmorelin in Japan in 2004.
- Dosing note
- No dosing instruction - clinical protocols used subcutaneous infusions (e.g. 1 µg/kg/h) and a diagnostic single-dose IV bolus; research/off-label protocols vary widely and should not be self-applied without medical supervision.
Use in the injection calculator
GHRP-2 (Pralmorelin) is a synthetic peptide hormone and ghrelin-receptor agonist from the growth-hormone secretagogue (GHS) class: the hexapeptide (D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2, ~818 Da) binds GHS-R1a and triggers pulsatile release of endogenous growth hormone (GH) from the pituitary - it does not deliver GH itself. In Japan it is approved as pralmorelin for the diagnosis of GH deficiency in adults and children aged 4 and over.
How does GHRP-2 work?
GHRP-2 acts on a different receptor than classical GHRH analogs such as tesamorelin or sermorelin. It activates the ghrelin receptor (GHS-R1a) in the anterior pituitary and hypothalamus. Downstream signaling runs primarily via cAMP, PLC and protein kinase C, producing:
- a sharp, short GH pulse (peak ~15-60 min),
- suppression of somatostatin tone,
- moderate co-stimulation of ACTH, cortisol and prolactin (weaker than GHRP-6, stronger than ipamorelin),
- increased appetite (ghrelin-like, but milder than GHRP-6).
What does the evidence say?
Compared with GHRP-6, GHRP-2 is the most potent classical GHRP by peak GH output while producing less appetite stimulation. The human evidence includes several small RCTs:
- Laferrère et al. (2005) showed that a subcutaneous GHRP-2 infusion increased ad-libitum food intake by ~36% in healthy lean men - a clear ghrelin-mimetic effect.
- Laferrère et al. (2006) confirmed that obese subjects also respond with increased food intake to the ghrelin agonist GHRP-2.
- Haruta et al. (2015) reported one year of intranasal GHRP-2 in a severely emaciated anorexia-nervosa patient, with improvements in body weight and hypoglycemia symptoms.
- Veldhuis et al. (2007) dissected how peripheral signals (e.g. estrogen receptor-α) modulate the waveform of GHRP-2-induced GH secretory bursts.
The Japanese diagnostic approval rests on Phase III data showing that a single IV bolus reliably separates GH-sufficient subjects (peak GH ≥ 15 µg/L) from those with severe adult GH deficiency (clearly below this cut-off).
What is GHRP-2 used for?
- Approved (Japan): diagnostic GH-stimulation test in adults and children ≥ 4 years (pralmorelin, Kaken Pharmaceutical).
- Clinically investigated: appetite stimulation in cachexia/anorexia, acute GH-pulse studies, combined provocation tests with GHRH/TRH.
- Off-label research: body composition, sleep architecture, recovery and tissue repair - none of these are FDA-approved indications.
In research protocols GHRP-2 is often combined with a GHRH analog such as CJC-1295 (without DAC) because the two receptor pathways are complementary and produce a stronger, more physiological GH pulse - a principle we also describe in the CJC-1295/Ipamorelin entry.
How safe is GHRP-2?
Published trial data show a generally favorable safety profile, but with the characteristic class effects of GHRPs:
- Increased appetite - sometimes desired, sometimes not.
- Moderate rises in cortisol and prolactin, clinically relevant with repeated high dosing.
- Flushing, water retention, tingling after bolus injection, usually transient.
- Possible glucose effects (transient insulin resistance, since GH is anti-insulinergic).
Long-term data on repeated use in healthy adults are sparse; diagnostic single doses are considered well tolerated.
Regulatory status
- Japan (PMDA, 10/2004): approved as pralmorelin for GH-deficiency diagnosis in adults and children ≥ 4 years.
- US / EU: no FDA or EMA approval; North American rights were once sublicensed to Wyeth but never progressed.
- Sport: GHRP-2 is on the WADA Prohibited List at all times (class S2: peptide hormones and growth factors).
How does GHRP-2 compare to GHRP-6 and ipamorelin?
- GHRP-2 vs GHRP-6: higher GH peak, less hunger, somewhat lower cortisol/prolactin rise.
- GHRP-2 vs ipamorelin: ipamorelin is far more selective (almost no cortisol/prolactin effect); GHRP-2 delivers a stronger raw GH pulse.
- GHRP-2 vs GHRH analogs such as tesamorelin: completely different receptor pathway (GHS-R1a vs GHRH-R), so the two are additive when combined.
Frequently asked questions about GHRP-2
Is GHRP-2 legal to buy?
Outside Japan there is no approved pharmaceutical form of GHRP-2. Depending on the country and formulation, it falls under different rules for peptide hormones; self-use without a medical indication and supervision is not recommended.
How long does a dose of GHRP-2 last?
Plasma half-life is very short (~15-60 min) and the GH pulse lasts roughly 1-2 hours. Research protocols therefore use multiple daily doses or combine GHRP-2 with a long-acting GHRH analog such as CJC-1295 with DAC for sustained GH-axis stimulation.
Is GHRP-2 the same as pralmorelin?
Yes. Pramlomrelin is the INN (International Nonproprietary Name) of GHRP-2 as a drug substance. In Japan it is marketed as GHRP Kaken by Kaken Pharmaceutical.
Disclaimer: Peptipedia provides general information on peptides - not medical advice and no dosing or sourcing recommendations. Talk to a clinician you trust before using any peptide.
Related peptides
Sources
- Bowers CY. History to the discovery of ghrelin. Methods Enzymol 2012 (PMID 22975043)
- Laferrère B et al. Growth hormone releasing peptide-2 (GHRP-2), like ghrelin, increases food intake in healthy men. J Clin Endocrinol Metab 2005 (PMID 15699539)
- Laferrère B et al. Obese subjects respond to the stimulatory effect of the ghrelin agonist growth hormone-releasing peptide-2 on food intake. Obesity 2006 (PMID 16861611)
- Haruta I et al. One-year intranasal application of growth hormone releasing peptide-2 improves body weight and hypoglycemia in a severely emaciated anorexia nervosa patient. J Cachexia Sarcopenia Muscle 2015 (PMID 26401470)
- Veldhuis JD et al. Peripheral estrogen receptor-alpha selectively modulates the waveform of GH secretory bursts in healthy women. Am J Physiol 2007 (PMID 17686882)
- Pralmorelin drug profile (PMID 15230633)