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GHRP-2

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

Quick Stats
Studies 230
Trials 1
Score 3
2006 pubmed 12 citations

Effects of combined long-term treatment with a growth hormone-releasing hormone analogue and a growth hormone secretagogue in the growth hormone-releasing hormone knock out mouse.

Fintini. Danilo D; Alba. Maria M; Schally. Andrew V AV; Bowers. Cyril Y CY; Parlow. A F AF; Salvatori. Roberto R

Key Findings

  • GHRP‑2 alone does not stimulate GH release in the absence of any GHRH signaling.
  • Combining a GHRH analogue (JI‑38) with GHRP‑2 produces greater growth (body length and weight) than GHRH alone in GHRH‑deficient mice.
  • Both treatment groups (GHRH alone or GHRH + GHRP‑2) corrected the under‑development of pituitary somatotrope cells.

Practical Outcomes

  • For biohackers, the study suggests that pairing a GHRH‑type peptide (e.g., CJC‑1295, Tesamorelin) with GHRP‑2 could boost growth‑hormone effects more than using GHRP‑2 alone. In people who already have normal GHRH, the added benefit may be modest, but the data support a synergistic approach for those seeking maximal GH output.

Summary

In mice that lack the natural hormone that tells the pituitary to release growth hormone, giving a synthetic GHRH drug (JI-38) helped the pituitary grow, and adding the GHRP‑2 peptide on top made the animals taller and heavier than GHRH alone. However, GHRP‑2 by itself could not trigger a growth‑hormone spike unless some GHRH was present.

Abstract

GH secretagogues (GHS) are synthetic ghrelin receptor agonists that stimulate GH secretion. It is not clear whether they act predominantly by stimulating the secretion of hypothalamic growth hormone-releasing hormone (GHRH), or directly on the somatotrope cells. In addition, it is not known whether combined treatment with GHRH and GHS has synergistic effects on growth. To address these questions, we used the GH-deficient GHRH knock out (GHRHKO) mouse model, which has severe somatotrope cell hypoplasia. We treated GHRHKO mice for 5 weeks (from week 1 to week 6 of age) with the GHRH analogue JI-38 alone, or in combination with a GHS (GHRP-2), and at the end of the treatment we examined their response to an acute stimulus with GHRP-2 or GHRP-2 plus JI-38. We used placebo-treated GHRHKO mice and animals heterozygous for the GHRHKO allele as controls. Animals treated with JI-38+GHRP-2 reached higher body length and weight than animals treated with JI-38 alone. All the animals receiving JI-38 (with or without GHRP-2) showed similar correction of somatotrope cell hypoplasia. None of the GHRHKO animals showed a serum GH response to the acute stimulation with GHRP-2 alone, while both treated groups responded to the combined test with JI-38 + GHRP-2. These data demonstrate that in GHRHKO mice, GHRP-2 has a growth-stimulating effect that augments the response induced by JI-38. In addition, the presence of GHRH seems necessary for the stimulation of GH secretion by GHRP-2.

Study Information

Provider

pubmed

Year

2006

Date

2006-04-03T00:00:00.000Z

DOI

10.1159/000092520

Citations

12

References

32