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Hexarelin

Examorelin, HEX

Quick Stats
Studies 233
Trials 61
Score 3
1999 pubmed

The growth hormone secretagogue hexarelin stimulates the hypothalamo-pituitary-adrenal axis via arginine vasopressin.

Korbonits. M M; Kaltsas. G G; Perry. L A LA; Putignano. P P; Grossman. A B AB; Besser. G M GM; Trainer. P J PJ

Key Findings

  • Hexarelin significantly raises ACTH and cortisol levels in healthy young males.
  • The cortisol increase is likely mediated by arginine vasopressin (AVP) rather than CRH.
  • Hexarelin also causes a clear rise in GH and prolactin, with a small acute increase in appetite.

Practical Outcomes

  • If you’re using hexarelin to boost GH for muscle or anti‑aging benefits, expect a concurrent rise in cortisol, which could affect stress, sleep, and muscle‑protein balance. Timing doses (e.g., early in the day) and monitoring cortisol or stress markers may help mitigate unwanted effects. The modest appetite boost might be useful if you’re aiming for a slight increase in caloric intake.

Summary

Hexarelin, a growth‑hormone‑releasing peptide, not only spikes GH but also triggers the stress‑hormone system (ACTH and cortisol) in healthy men. The cortisol boost seems to come from stimulating the brain’s vasopressin pathway rather than the usual CRH route, and the peptide also nudges appetite a bit higher.

Abstract

GH secretagogues (GHSs) act via specific receptors in the hypothalamus and the pituitary gland to release GH. GHSs also stimulate the hypothalamo-pituitary-adrenal (HPA) axis via central mechanisms probably involving CRH or arginine vasopressin (AVP). We studied the effects of hexarelin, CRH, and desmopressin, an AVP analog, on the stimulation of the HPA axis in 15 healthy young male volunteers. Circulating ACTH, cortisol, GH and PRL concentrations were measured for 2 h after the injection of hexarelin, CRH, or desmopressin alone and the combination of hexarelin plus CRH or hexarelin plus desmopressin. Symptoms during the tests were assessed by visual analog scales. Hexarelin significantly increased ACTH and cortisol release (area under the curve, 3,444+/-696 ng/L x 125 min and 45,844+/-2,925 nmol/L x 125 min, respectively), and this effect was augmented by the addition of CRH in a dose that on its own produces maximal stimulation (6,580+/-1,572 ng/mL x 125 min and 63,170+/-2,616 nmol/L x 125 min; P = 0.01 and 0.001, respectively), but was not influenced by the addition of desmopressin (3,540+/-852 ng/mL x 125 min and 35,319+/-3,252 nmol/L x 125 min; not significant). CRH on its own caused similar or slightly higher ACTH and cortisol release than hexarelin alone. Desmopressin given alone elicited a rapid rise in circulating ACTH and cortisol, but its effects were less than those of any other treatment and were not augmented by hexarelin. Hexarelin also caused significant GH and PRL release, but these effects were not influenced by the coadministration of CRH or desmopressin. Visual analog scales showed an acute small increment in appetite with hexarelin. Our data suggest that the effect of GHSs on the HPA axis involve at least in part the stimulation of AVP release. In summary, we have shown that in healthy male volunteers, the effect of hexarelin on the HPA axis does not involve CRH, but may occur through the stimulation of AVP release.

Study Information

Provider

pubmed

Year

1999

DOI

10.1210/jcem.84.7.5811