GHRP-6
Growth Hormone Releasing Peptide-6, Growth hormone-releasing hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2
Do growth hormone-releasing peptides act as ghrelin secretagogues?
Ahnfelt-Rønne. I I; Nowak. J J; Olsen. U B UB
Key Findings
- GHRP‑6 and a related compound accumulate in the glandular part of the stomach, the main site of ghrelin synthesis.
- Removing the gastrointestinal tract cuts the GH‑releasing response to GHRP‑6 by about 60‑70%, while GH‑releasing hormone is unaffected.
- These results suggest that ghrelin released from the stomach mediates a significant portion of GHRP‑6’s growth‑hormone‑stimulating effect.
Practical Outcomes
- For biohackers, the takeaway is that gut health and timing matter: taking GHRP‑6 on an empty stomach or ensuring a healthy stomach lining may maximize GH release. It also hints that conditions that impair ghrelin production (e.g., chronic gastritis, certain surgeries) could blunt GHRP‑6 effectiveness.
Summary
The study shows that GHRP‑6 gathers in the stomach where ghrelin (the body’s natural growth‑hormone‑releasing hormone) is made, and that cutting out the gut dramatically reduces GHRP‑6’s ability to boost growth hormone. This means part of GHRP‑6’s effect depends on a healthy stomach and its ghrelin production.
Abstract
NN703 is an orally active and selective growth hormone secretagogue (GHS) that was derived from growth hormone-releasing peptide-1(GHRP-1) via ipamorelin by a peptidomimetic approach and has now entered into phase II clinical trials. When the disposition in rats of NN703 and GHRP-6 was studied using whole-body autoradiography following administration of an iv dose of radiolabeled material, we found that a substantial amount of these secretagogues accumulate in the glandular part of the stomach. Because this is the site of synthesis and secretion of ghrelin, the endogenous GHS, we investigated the effect of resection of the gastrointestinal (GI) tract on growth hormone (GH) release induced by GHRP-6. This procedure significantly attenuated the GH secretion response by 60-70%. By contrast, the effect of GH-releasing hormone on GH release was not inhibited. The binding of GHRPs to the glandular part of the stomach and the blunted GH response to GHRP-6 following resection of the GI tract suggest a role for ghrelin as a mediator of part of the GH-releasing effect of GHRPs.
Study Information
pubmed
2001
10.1385/endo:14:1:133