GHRP-6
Growth Hormone Releasing Peptide-6, Growth hormone-releasing hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2
Effects of growth hormone secretagogues on the release of adenohypophyseal hormones in young and old healthy dogs.
Bhatti. Sofie F M SF; Duchateau. Luc L; Van Ham. Luc M L LM; De Vliegher. Sarne P SP; Mol. Jan A JA; Rijnberk. Ad A; Kooistra. Hans S HS
Key Findings
- Ghrelin triggers the biggest GH surge in young dogs, more than GHRP-6 or GHRH.
- In older dogs, GHRH produces the highest GH levels; GHRP-6 still works but is less potent.
- All three growth‑hormone secretagogues (including GHRP-6) do not significantly raise ACTH, cortisol, TSH, LH, or prolactin.
Practical Outcomes
- For biohackers, the data suggest GHRP-6 can still be used to boost GH in older individuals, though the effect may be modest compared to younger users or other secretagogues. It appears hormone‑specific, so major side‑effects on other pituitary axes are unlikely, but human studies are needed to confirm dosing and age‑related efficacy.
Summary
In a study on young and old dogs, the peptide GHRP-6 did raise growth hormone (GH) levels, but it wasn’t as strong as ghrelin in young dogs or GHRH in older dogs. Importantly, GHRP-6 didn’t cause spikes in other hormones like ACTH, cortisol, or prolactin, suggesting a fairly specific GH effect. The age‑related drop in GH response was biggest for ghrelin, while GHRP-6’s drop was smaller.
Abstract
The effects of three growth hormone secretagogues (GHSs), ghrelin, growth hormone-releasing peptide-6 (GHRP-6), and growth hormone-releasing hormone (GHRH), on the release of adenohypophyseal hormones, growth hormone (GH), adrenocorticotropic hormone (ACTH), thyroid-stimulating hormone (TSH), luteinising hormone (LH), prolactin (PRL) and on cortisol were investigated in young and old healthy Beagle dogs. Ghrelin proved to be the most potent GHS in young dogs, whereas in old dogs GHRH administration was associated with the highest plasma GH concentrations. The mean plasma GH response after administration of ghrelin was significantly lower in the old dogs compared with the young dogs. The mean plasma GH concentration after GHRH and GHRP-6 administration was lower in the old dogs compared with the young dogs, but this difference did not reach statistical significance. In both age groups, the GHSs were specific for GH release as they did not cause significant elevations in the plasma concentrations of ACTH, cortisol, TSH, LH, and PRL. It is concluded that in young dogs, ghrelin is a more powerful stimulator of GH release than either GHRH or GHRP-6. Ageing is associated with a decrease in GH-releasing capacity of ghrelin, whereas this decline is considerably lower for GHRH or GHRP-6.
Study Information
pubmed
2005
2005-06-13T00:00:00.000Z
10.1016/j.tvjl.2005.04.025