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GHRP-6

Growth Hormone Releasing Peptide-6, Growth hormone-releasing hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2

Quick Stats
Studies 702
Trials 0
Score 3
1996 pubmed 10 citations

Hypothalamic control of growth hormone (GH) secretion in type I diabetic men: effect of the combined administration of GH-releasing hormone and hexarelin, a novel GHRP-6 analog.

Giustina. A A; Desenzani. P P; Perini. P P; Deghenghi. R R; Bugari. G G; Wehrenberg. W B WB; Giustina. G G

Key Findings

  • Hexarelin (a GHRP‑6 analog) produced a larger GH response than GHRH alone in both diabetic and normal men.
  • Combining hexarelin with GHRH raised GH levels higher than either peptide given by itself.
  • The interaction was synergistic in healthy subjects but only additive in type‑I diabetic subjects.

Practical Outcomes

  • For biohackers, the data support using a GHRP‑6 peptide together with a GHRH peptide (e.g., CJC‑1295) to achieve stronger GH pulses than either alone. While the study used IV dosing, typical sub‑Q doses (100‑300 µg hexarelin/GHRP‑6 and 100‑200 µg GHRH) are likely sufficient to see a similar additive effect. Expect greater GH spikes, but remember the sample size is tiny and the population was diabetic, so individual responses may vary.

Summary

In a small study of men with type‑I diabetes and healthy controls, giving the GHRP‑6‑like peptide hexarelin boosted growth hormone (GH) more than giving GHRH alone, and the two together pushed GH even higher. The combo worked best in healthy people (synergistic) and still helped diabetics (additive). This suggests that stacking a GHRP‑6 peptide with a GHRH peptide can amplify GH spikes.

Abstract

Insulin dependent (type I) diabetic patients show abnormal growth hormone (GH) secretion. Hexarelin is an analog of GHRP-6 which releases GH in part via somatostatin inhibition. The aim of our study was to evaluate the effects of hexarelin and GHRH, administered either alone or in combination, on GH secretion in 10 type I diabetic and 7 normal men. All the subjects were administered: 1) human GHRH (1-29) NH2 100 micrograms i.v. bolus at 0 min; 2) hexarelin 100 micrograms i.v. bolus at 0 min; 3) hexarelin 100 micrograms + hGHRH 100 micrograms i.v. bolus at 0 min. In type I diabetic patients significantly greater GH responses to GHRH and hexarelin have been observed with normal subjects. Hexarelin caused a significantly (p < 0.05) greater GH response as compared to GHRH in both diabetic and control subjects. After the administration of hexarelin+GHRH, a significant increase in both GH absolute and peak levels as compared to hexarelin or GHRH alone was found in all the subjects. However, the GH responses to the combined stimuli were not significantly different in diabetics as compared to normals; moreover, the interaction of GHRH and hexarelin was synergistic in controls and additive in diabetics. We hypothesize that a reduction in the hypothalamic somatostatin inhibitory tone combined with increased pituitary GH production may be responsible for the pattern of the GH responses to hexarelin and GHRH observed in our type I diabetic patients.

Study Information

Provider

pubmed

Year

1996

Date

1996-05-01T00:00:00.000Z

DOI

10.1080/07435809609030505

Citations

10

References

33