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GHRP-2

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

Quick Stats
Studies 230
Trials 1
Score 2
1998 pubmed

Effects of eight months treatment with graded doses of a growth hormone (GH)-releasing peptide in GH-deficient children.

Mericq. V V; Cassorla. F F; Salazar. T T; Avila. A A; Iñiguez. G G; Bowers. C Y CY; Merriam. G R GR

Key Findings

  • GHRP‑2 caused a dose‑dependent increase in overnight GH secretion in GH‑deficient children.
  • The GH surge was brief, with little effect later in the night, and IGF‑I and IGFBP‑3 levels did not rise.
  • Growth velocity improved during treatment, and no toxicity or side effects were observed.

Practical Outcomes

  • For biohackers, this study confirms that GHRP‑2 can safely trigger a short GH pulse, but it likely won’t sustain IGF‑1‑mediated growth or long‑term anabolic effects in healthy adults. To be useful for performance or anti‑aging, formulations that extend the GH‑release window would be needed.

Summary

In a small study of six GH‑deficient kids, daily injections of GHRP‑2 raised nighttime GH levels in a dose‑dependent way, but the boost was short‑lived and didn’t raise IGF‑1. The kids grew a bit faster while on the peptide and showed no side effects.

Abstract

Stimulation of pituitary GH secretion with administered GHRH can be effective therapy for those GH deficient (GHD) patients whose disorder results from insufficient endogenous GHRH secretion. We have previously shown that most such patients also respond acutely to the GH-releasing peptides (GHRP's), which have a different mechanism of action from GHRH, with release of GH. In this study we tested whether the GH response to a newer GHRP, GHRP-2, would be sustained over time. Six prepubertal children with GHD and growth failure received stepwise increasing s.c. doses of GHRP-2, at 0.3, 1.0, and 3.0 micrograms/kg/day, in successive 2-month treatment periods, with monitoring of overnight 12 h episodic GH secretion and toxicity measures at the end of each period. During a fourth 2-month period, they received 3 micrograms/kg GHRP-2 together with 3 micrograms/kg s.c. GHRH. Serum levels of IGF-I and IGFBP-3 were also measured, and stadiometer height measurements were recorded. GHRP-2 administration produced a dosewise increase in overnight GH secretion. GH profiles showed that the effect of GHRP-2 injections was relatively brief, with little effect upon GH secretion later in the night. Serum levels of IGF-I and of IGFBP-3 did not increase. Growth velocity was higher during GHRP-2 treatment than during pretreatment and post-treatment evaluations. There were no side effects or toxicities observed. Thus GHRP-2 is well tolerated and is able to stimulate GH secretion. Formulations or routes of administration that allow for a longer duration of action will likely be needed to use GHRP-2 in therapy.

Study Information

Provider

pubmed

Year

1998

DOI

10.1210/jcem.83.7.4969