GHRP-6
Growth Hormone Releasing Peptide-6, Growth hormone-releasing hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2
Effect of combined administration of growth hormone (GH)-releasing hormone, GH-releasing peptide-6, and pyridostigmine in normal and obese subjects.
Cordido. F F; Peñalva. A A; Peino. R R; Casanueva. F F FF; Dieguez. C C
Key Findings
- Combined GHRH + GHRPâ6 produces a strong, rapid GH surge in both normal and obese subjects.
- Pyridostigmine (a somatostatinâtone blocker) does not increase the GH response beyond GHRH + GHRPâ6 alone.
- Obese individuals have a significantly smaller GH peak and total GH output compared to lean controls.
Practical Outcomes
- For biohackers aiming to raise GH, using GHRPâ6 together with a GHRH analogue is effective without needing additional drugs like pyridostigmine. Expect the GH peak about 30âŻminutes after injection in lean people and around 15âŻminutes in obese people, but the overall response will be lower in obesity. This protocol can be used for shortâterm GH spikes to support recovery, muscle growth, or fat loss, keeping in mind the reduced efficacy in higher body fat.
Summary
Giving the peptide GHRPâ6 together with a growthâhormoneâreleasing hormone (GHRH) shot makes the body release a big burst of growth hormone, and this works even if you block somatostatin with pyridostigmine. In lean people the peak GH is about 75âŻÂ”g/L at 30âŻmin, while in obese people the peak is roughly half that (â42âŻÂ”g/L) and the overall GH exposure is lower. Adding pyridostigmine doesnât boost the response any further.
Abstract
Growth hormone (GH) secretion in response to all provocative stimuli is decreased in patients with obesity. Recently, we found that the combined administration of GH-releasing hormone (GHRH) and the hexapeptide GH-releasing peptide-6 (GHRP-6) induced a large increase in plasma GH levels. To gain further insight into the disrupted mechanism of GH regulation in obesity, we investigated whether the inhibition of somatostatinergic tone with pyridostigmine could further increase the GH response to combined administration of GHRH and GHRP-6. In normal subjects, administration of GHRH plus GHRP-6 induced a marked increase in plasma GH with a peak at 30 minutes (mean +/- SEM, 76.7 +/- 9.7 micrograms/L), which was similar to that obtained after pretreatment with pyridostigmine (74.7 +/- 9.4 micrograms/L). In obese patients, combined administration of GHRH plus GHRP-6 induced a clear increase in GH secretion with a peak at 15 minutes of 42.2 +/- 10.0 micrograms/L, which was also unaffected after pretreatment with pyridostigmine (38.4 +/- 5.8 micrograms/L). The GH response was lower in obese patients than in controls as assessed by the area under the curve after administration of both GHRH plus GHRP-6 (1,846 +/- 396 v 4,773 +/- 653, P < .01) and pyridostigmine plus GHRH plus GHRP-6 (1,989 +/- 372 v 5,098 +/- 679, P < .005). In conclusion, these data suggest that GHRP-6 can behave as a functional somatostatin antagonist, and that somatotrope responsiveness to the combined administration of GHRH plus GHRP-6 is largely independent of somatostatinergic tone.(ABSTRACT TRUNCATED AT 250 WORDS)
Study Information
pubmed
1995
1995-06-01T00:00:00.000Z
10.1016/0026-0495(95)90187-6
36
28