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GHRP-2

Pralmorelin, Growth Hormone Releasing Peptide-2, KP-102

Quick Stats
Studies 230
Trials 1
Score 4
1993 pubmed

GH releasing peptides--structure and kinetics.

Bowers. C Y CY

Key Findings

  • All three GHRPs (GHRP‑1, GHRP‑2, GHRP‑6) release GH more effectively than the standard GHRH‑1‑44 peptide in humans.
  • Oral administration of GHRP‑2 (and the other GHRPs) produces a robust GH surge, comparable to injectable routes.
  • A synergistic GH boost occurs when a low‑dose IV bolus of GHRP‑1 is given together with GHRH‑1‑44.

Practical Outcomes

  • For self‑experimenters, oral GHRP‑2 can be used as a convenient way to spike GH without injections, making it suitable for daily protocols aimed at muscle growth, fat loss, or recovery. Pairing a small dose of GHRP‑1 (or GHRP‑2) with a GHRH analogue could further amplify GH release, offering a potential strategy for maximal hormonal response. Dosing appears effective at microgram per kilogram levels, but users should start low and monitor side effects.

Summary

GHRP-2 (and its siblings GHRP-1 and GHRP-6) are tiny synthetic peptides that reliably boost growth hormone (GH) when taken by injection or even by mouth. They work in both animals and humans, and the oral form can produce near‑maximal GH spikes. Combining a tiny dose of GHRP‑1 with the natural GH‑releasing hormone (GHRH) makes the effect even stronger.

Abstract

A new class of small synthetic peptides has been developed which specifically release GH. They consist of 6-7 amino acids and release GH in animals as well as humans. So far 3 of these peptides have been administered to humans, i.e., GHRP-6, GHRP-1 and GHRP-2. As in rats, these 3 peptides have been found to be increasingly more effective in releasing GH in humans. All 3 GHRPs release GH more efficaciously than GHRH 1-44 NH2 in humans. Particularly note-worthy is that GHRP-6, GHRP-1 AND GHRP-2 all release GH after oral administration. Near maximal amounts of GH can be released after GHRP-1 and GHRP-2 oral administration. In the present studies, the GH responses and serum irGHRP levels after i.v., s.c. and oral administration have been determined in normal younger men and/or women. By each route of administration GH was very effectively released. Additionally, GH release was induced by oral GHRP-6 in children with various degrees of GH deficiency. Noteworthy is the synergistic release of GH induced by the combined i.v. bolus administration of 1 microgram/kg of GHRP-1 + GHRH 1-44NH2. Thus, these results demonstrate GHRPs' potential importance at the theoretical as well as pharmaceutical level.

Study Information

Provider

pubmed

Year

1993

DOI

10.1515/jpem.1993.6.1.21