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Hexarelin

Examorelin, HEX

Quick Stats
Studies 233
Trials 61
Score 3
1994 pubmed

Growth hormone releasing activity by intranasal administration of a synthetic hexapeptide (hexarelin).

Laron. Z Z; Frenkel. J J; Gil-Ad. I I; Klinger. B B; Lubin. E E; Wuthrich. P P; Boutignon. F F; Lengerts. V V; Deghenghi. R R

Key Findings

  • Intranasal hexarelin (20 µg/kg) produced a strong GH increase, similar in size to an IV dose (1 µg/kg).
  • Peak GH after nasal dosing occurred later (30‑60 min) than after IV dosing (15‑30 min).
  • GH‑deficient adults showed no GH response, indicating the effect may depend on a functional pituitary.
  • TSH fell modestly during both tests but stayed within normal limits; free T4 and T3 were unchanged.

Practical Outcomes

  • For biohackers, intranasal hexarelin could be a non‑invasive way to spike GH, potentially aiding muscle growth or recovery, but the data are limited to children and short‑term hormone changes. The effective dose reported is 20 µg per kilogram body weight, and safety, long‑term effects, and efficacy in healthy adults remain untested. Use with caution and consider medical supervision.

Summary

A tiny synthetic peptide called hexarelin can boost growth hormone (GH) when sprayed into the nose, working almost as well as an IV injection. In a small study of 12 people (mostly kids with short stature), GH rose sharply, while thyroid hormone levels stayed normal. Adults who truly lack GH did not respond.

Abstract

Hexarelin is a new synthetic growth hormone releasing peptide. We have tested the efficacy of intranasal (i.n.) administration of hexarelin to stimulate plasma GH and have compared this to the intravenous (i.v.) administration of the peptide. Ten children with familial short stature (FSS) aged 5.5-15.5 years and two known GH deficient patients aged 24 and 28 years without GH treatment. All 12 subjects were submitted to i.v. (1 microgram/kg) and i.n. (20 micrograms/kg) hexarelin tests with a one-week interval between tests. Blood samples for GH, TSH, fT4 and T3 were obtained at 0, 15, 30, 60, 90 and 120 minutes. The hormone determinations were made by standard radio-immunoassays (RIA). Both the i.n. and i.v. administration of hexarelin induced a large GH response, the mean (+/- SD) being 72.2 +/- 35.5 mU/l for the i.n. test and 79.6 +/- 53.0 mU/l for the i.v. test. The peak GH in the i.v. test occurred at 15-30 minutes and in the i.n. test between 30 and 60 minutes. The GH deficient patients showed no GH response in either test. Plasma TSH decreased in the FSS children from a mean (+/- SD) of 1.0 +/- 0.26 to 0.64 +/- 0.2 mU/l (P < 0.005) during the i.n. test and from 1.0 +/- 0.3 to 0.7 +/- 0.3 mU/l (P < 0.05) during the i.v. test. In the isolated GH deficient patient, plasma TSH decreased from 1.06 +/- 0.38 mU/l to 0.86 +/- 0.17 during the i.v. test and from 1.60 +/- 0.01 to 1.11 +/- 0.06 mU/l during the i.n. test. There were no significant changes in plasma fT4 or T3 in any of the tests. The synthetic hexapeptide hexarelin is a potent pituitary GH stimulator when administered intranasally. The GH response was similar to that observed after intravenous hexarelin. Simultaneously, there was a significant decrease in plasma TSH but the concentrations remained in the normal range. These findings appear to be of theoretical and practical relevance to the investigation and management of short children.

Study Information

Provider

pubmed

Year

1994

DOI

10.1111/j.1365-2265.1994.tb02589.x