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Hexarelin

Examorelin, HEX

Quick Stats
Studies 233
Trials 61
Score 3
1996 pubmed

Desensitization from long-term intranasal treatment with hexarelin does not interfere with the biological effects of this growth hormone-releasing peptide in short children.

Klinger. B B; Silbergeld. A A; Deghenghi. R R; Frenkel. J J; Laron. Z Z

Key Findings

  • Long‑term daily intranasal hexarelin causes partial desensitization, lowering the acute GH spike to both nasal and IV doses.
  • Despite the reduced GH spikes, growth velocity increased significantly during treatment.
  • GH responsiveness partially recovers a few months after stopping the peptide.

Practical Outcomes

  • Continuous daily dosing of hexarelin may blunt its ability to trigger big GH releases, so biohackers might use intermittent or cycled schedules to keep the response strong. Even with some desensitization, the peptide can still boost growth or lean‑mass related outcomes, but watch for diminishing hormone spikes over time.

Summary

A study gave short kids a nasal peptide called hexarelin every day for up to 10 months. Over time their bodies got used to it and released less growth hormone when given a dose, but they still grew taller faster than before. After stopping the peptide, the hormone response started to come back.

Abstract

A clinical, prospective experiment was carried out to determine whether long-term intranasal administration of the growth hormone-releasing peptide hexarelin (His-D-2-methyl-Trp-Ala-Trp-D-Phe -Lys-NH2) affects pituitary growth hormone secretion. Hexarelin (60 micrograms/kg t.i.d.) was administered to seven prepubertal constitutionally short children (mean age +/- SD = 7.6 +/- 2.4 years). Serum human growth hormone (hGH) response to an intranasal (20 micrograms/kg) and i.v. (1 mircogram/kg) bolus of hexarelin before, during and after 6-10 months of treatment was measured. The mean ( +/- SD) peak rise of hGH to the intranasal bolus before treatment was 70.6 +/- 28.2 mU/l. After 7 days of hexarelin treatment, mean peak values dropped to 34.1 +/- 15.7 mU/l (p < 0.002) and thereafter remained constant for 6 months of treatment at 37.5 +/- 10.3 mU/l (p < 0.03). The pretreatment peak to th i.v. hexarelin bolus was 84.8 +/- 52.5 mU/l, and at the end of the treatment period it was 19.8 +/- 10.9 mU/l (p < 0.05). Three months after stopping treatment the mean ( +/- SD) hGH response rose to 42.1 +/- 4.7 mU/l (p < 0.005). Growth velocity increased from 5.3 +/- 0.9 cm/year (before treatment) to 7.4 +/- 1.6 cm/year at 6-10 months of treatment (p < 0.005). In conclusion, teh partial suppression of pituitary hGH responsiveness to long-term intranasal hexarelin treatment, probably due to desensitization, does not affect the observed increase in growth velocity.

Study Information

Provider

pubmed

Year

1996

DOI

10.1530/eje.0.1340716