The GH-releasing effect of Hexarelin, a synthetic hexapeptide, in newborns is lower than in young adults.
Bartolotta. E E; Bellone. J J; Aimaretti. G G; Arvat. E E; Benso. L L; Deghenghi. R R; Camanni. F F; Ghigo. E E
Key Findings
- Newborns have very high baseline GH but low IGF‑1 compared to older groups.
- Hexarelin raises GH less in newborns than in pre‑pubertal children or young adults.
- In pre‑pubertal children and adults, hexarelin induces a larger GH surge than GHRH, indicating an age‑dependent response.
- The GH‑releasing action of hexarelin does not appear to be mediated by endogenous GHRH release.
Practical Outcomes
- For biohackers, hexarelin can be considered an effective GH‑secretagogue in adolescents and adults, but its potency may vary with age. It’s not useful for infants, and its mechanism is independent of GHRH, so combining it with GHRH‑based strategies may not be synergistic. Standard dosing used in research (≈2 µg/kg IV) may need adjustment for subcutaneous use, and safety data remain limited.
Summary
Hexarelin, a synthetic peptide, can raise growth hormone (GH) levels in adults, but it works less well in newborns. In kids and adults, it actually triggers more GH than the natural hormone GHRH, while newborns respond better to GHRH than to hexarelin. This shows the peptide’s effect changes with age and isn’t just causing the body to release its own GHRH.
Abstract
The aim of the present study was to verify the GH-releasing effect of Hexarelin, a synthetic hexapeptide, in newborns who are known to have GH hypersecretion likely due to hyperactivity of GHRH-secreting neurons while somatostatinergic activity seems not fully operative. We studied in 6 newborns (NB, 2.5 +/- 2.1 days), 12 prepubertal children (PC, 9.8 +/- 0.45 yr) and 12 young adults (YA, 28.2 +/- 0.2 yr) the GH response to Hexarelin (HEX, 2 micrograms/kg i.v.) compared to that observed after GHRH (1 microgram/kg i.v.) in 6 NB (4.2 +/- 0.4 days), 12 PC (9.9 +/- 0.6 yr) and 12 YA (31.0 +/- 1.3 yr). GH levels were assayed basally and 30 and 60 min after drug administration. In NB, mean (+/- SEM) basal GH levels were higher while IGF-I levels were lower than those recorded in PC and YA (GH: 34.8 +/- 1.9 vs 2.8 +/- 0.4 vs 1.4 +/- 0.4 micrograms/l, p < 0.0006; IGF-I: 36.3 +/- 1.9 vs 152.0 +/- 11.5 vs 175.8 +/- 15.3 micrograms/l, p < 0.0007); in the last two groups GH and IGF-I levels were similar. The mean delta GH peak after HEX in NB (32.8 +/- 4.7 micrograms/l) was similar to that in PC (34.6 +/- 4.3 micrograms/l) and lower (p < 0.01) than that in YA (56.2 +/- 7.4 micrograms/l). Delta GH peak after GHRH in NB (60.1 +/- 1.5) was higher than those in PC and YA (20.8 +/- 4.8 and 22.8 +/- 3.4 micrograms/l) (p < 0.005 and < 0.002, respectively). In NB, the GH response to HEX was lower (p < 0.005) than to GHRH while in PC and YA the somatotrope response to HEX was higher (p < 0.03 and 0.0004, respectively) than to GHRH. These data demonstrate that the GH-releasing effect of Hexarelin undergoes age-dependent variation being lower in newborns than in young adults, opposite to that observed after GHRH administration. The evidence that Hexarelin releases less GH than GHRH in newborns but not in prepubertal children and in young adults makes unlikely the hypothesis that the GH-releasing effect of this hexapeptide is mediated via endogenous GHRH release.
Study Information
pubmed
1997
10.1515/jpem.1997.10.5.491