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Sermorelin

GHRH (1-29), GRF 1-29 NH2, Sermorelin acetate

Quick Stats
Studies 223
Trials 41
Score 3
1993 pubmed 11 citations

Pharmacokinetics of growth hormone-releasing hormone(1-29)-NH2 and stimulation of growth hormone secretion in healthy subjects after intravenous or intranasal administration.

Wilton. P P; Chardet. Y Y; Danielson. K K; Widlund. L L; Gunnarsson. R R

Key Findings

  • IV sermorelin as low as 0.25 µg/kg triggers measurable GH release; peak GH (~90 mU/L) seen at 1‑2 µg/kg IV
  • Nasal absorption is poor (3‑5% bioavailability); a dose of ~50 µg/kg nasally matches the GH response of 1 µg/kg IV
  • Repeated nasal dosing maintains GH secretion without suppressing nighttime GH pulses

Practical Outcomes

  • For biohackers wanting a non‑injectable GH boost, intranasal sermorelin is possible but requires a relatively high dose due to low absorption. This makes it less cost‑effective than injections, but it could be useful for short‑term or experimental protocols where convenience outweighs efficiency. More data on long‑term safety and optimal dosing are needed before routine use.

Summary

The study shows that the growth‑hormone‑releasing peptide sermorelin can raise GH levels when given by IV or nasal spray. A tiny IV dose (0.25 µg/kg) works, but the nasal route only absorbs 3‑5% of the drug, so you need a much larger dose (about 50 µg/kg) to get a similar GH spike. Repeated nasal doses keep GH up without night‑time suppression, suggesting a convenient, injection‑free way to stimulate GH, though the high dose needed may limit practicality.

Abstract

The growth hormone-releasing hormone analogue GHRH(1-29)-NH2 was administered intravenously or intranasally to 30 healthy men aged 19-43 years. Intravenous injection of the lowest dose tested, 0.25 microgram/kg body weight, elicited significant release of growth hormone (GH). Maximal release (mean GH peaks of about 90 mU/l) was obtained with a dose of 1-2 micrograms/kg. Although GHRH(1-29)-NH2 was rapidly eliminated after intravenous injection, GH levels were elevated for about 3 hours. Absorption of GHRH(1-29)-NH2 through the nasal mucosa was found to be low, and the bioavailability was only 3-5%. There was a dose-dependent release of GH after intranasal administration of GHRH(1-29)-NH2, with the maximal response obtained with about 50 micrograms/kg; this dose was approximately as potent as 1 microgram/kg injected intravenously. The GH response after repeated intranasal administration of GHRH(1-29)-NH2 was sustained; there was no suppression of GH secretion during the night following a day when GHRH(1-29)-NH2 had been given three times intranasally. Based on these findings and the obvious convenience of intranasal administration compared with injections, it would be justified to test intranasal therapy for treatment of short stature in children with GH deficiency caused by hypothalamic damage.

Study Information

Provider

pubmed

Year

1993

Date

1993-06-01T00:00:00.000Z

DOI

10.1111/j.1651-2227.1993.tb12827.x

Citations

11

References

15