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GHRP-6

Growth Hormone Releasing Peptide-6, Growth hormone-releasing hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2

Quick Stats
Studies 702
Trials 0
Score 4
1993 pubmed

Massive growth hormone (GH) discharge in obese subjects after the combined administration of GH-releasing hormone and GHRP-6: evidence for a marked somatotroph secretory capability in obesity.

Cordido. F F; Peñalva. A A; Dieguez. C C; Casanueva. F F FF

Key Findings

  • GHRP‑6 alone caused a higher GH peak (≈15.7 ”g/L) than GHRH alone (≈6.8 ”g/L) in obese subjects.
  • Pre‑treating with pyridostigmine (a cholinesterase inhibitor) roughly doubled the GH response to GHRP‑6.
  • Combining GHRP‑6 with GHRH produced a massive GH release (average peak ≈42 ”g/L), far above any single stimulus.
  • The impaired GH secretion in obesity appears functional and reversible when these agents are used.

Practical Outcomes

  • For biohackers, using GHRP‑6 can robustly raise GH levels, and pairing it with a GHRH analogue may give an even larger spike. Adding a cholinergic enhancer like pyridostigmine could further amplify the effect, though the study used IV dosing, so sub‑Q routes should be tested cautiously. This protocol suggests a way to overcome the GH‑deficit seen in obesity, but safety and medical supervision remain essential.

Summary

In obese people, a synthetic peptide called GHRP‑6 makes the body release a lot of growth hormone, even more than the usual hormone‑releasing signal (GHRH). When GHRP‑6 is taken together with GHRH, the GH surge is huge, and a drug that boosts nerve signaling (pyridostigmine) can double the effect of GHRP‑6 alone. This shows that the low GH seen in obesity isn’t permanent and can be turned on again with the right mix of compounds.

Abstract

GH secretion in response to all provocative stimuli is decreased in patients with obesity. However, the precise mechanism causing this impairment in GH release is unknown. His-DTrp-Ala-Trp-DPhe-Lys-NH2 (GHRP-6) is a synthetic compound that releases GH in a dose-related and specific manner in several species, including man. To gain further insight into disrupted GH secretion in obesity, GHRP-6 and GH-releasing hormone (GHRH) at a dose of 100 micrograms, i.v., were administered either alone or in combination in a group of 19 obese subjects. In a group of obese patients, GHRP-6 induced GH secretion, with a GH peak (mean +/- SEM) of 15.7 +/- 4.4 micrograms/L and an area under the curve (AUC) of 674 +/- 187, which were larger than those after GHRH stimulation (6.8 +/- 1.1 and 412 +/- 71, respectively). Enhancement of the endogenous cholinergic tone was obtained in another group of obese subjects by means of pyridostigmine (120 mg, orally). Pyridostigmine administered 60 min before GHRP-6, increased both the mean GH peak (32.2 +/- 6.9) and the AUC (1413 +/- 537) after GHRP-6 administration. In a separate group of subjects, the combined administration of GHRP-6 and GHRH induced a massive discharge of GH, with individual responses ranging from 14-86 micrograms/L. GHRP-6 plus GHRH induced a mean GH peak of 42.2 +/- 10.9 and an AUC of 1894 +/- 784 (P < 0.05), clearly indicating a potentiating (synergic) action when the two compounds were administered together. These data show that GH responses to GHRP-6 were almost twice those to GHRH in obese patients. The stimulatory effect exerted by pyridostigmine on GHRP-6-induced GH secretion supported the view of increased somatostatinergic tone in obesity. Finally, the massive GH discharge that followed the administration of GHRH plus GHRP-6 was not observed after any stimulus in obesity, clearly indicating that the impaired GH secretion is a functional and potentially reversible state.

Study Information

Provider

pubmed

Year

1993

DOI

10.1210/jcem.76.4.8473389