Study summary · research use only
Hexarelin, a novel GHRP-6 analog, counteracts the inhibitory effect of hydrocortisone on growth hormone secretion in acromegaly
Plain-language summary
Paraphrased from the published abstract below — not a verdict on whether anything works.
This human study in ten patients (5 males, 5 females; age range 27-71 years) with active acromegaly examined whether hexarelin (His-D-2-Methyl-Trp-Ala-Trp-D-Phe-Lys-NH2), a GHRP-6 analog, counteracts hydrocortisone's inhibitory effect on GH secretion. Patients underwent hydrocortisone alone, hexarelin plus hydrocortisone, and hexarelin alone protocols with defined IV dosing. The mean GH peak (percent change from baseline) after hexarelin (1750 +/- 1157%) did not differ significantly from hexarelin plus hydrocortisone (1120 +/- 770%), while hydrocortisone alone was associated with a mean GH decrease of 47 +/- 7% from baseline. The authors reported the GH response to hexarelin in acromegaly was resistant to acute and sustained cortisol elevation, and suggested this supports hexarelin-induced reduction in endogenous somatostatin tone.
Abstract
Hexarelin (His-D-2-Methyl-Trp-Ala-Trp-D-Phe-Lys-NH2) is a GHRP-6 analog with the substitution of D-tryptophan with its 2-methyl derivative. The aim of our study was to ascertain whether hexarelin was able to counteract the glucocorticoid-mediated increase in hypothalamic somatostatin tone and consequent inhibition on serum GH levels in acromegalic patients. Ten patients (5 males, 5 females; age range 27-71 years; BMI range 23.3-35 kg/m2) with active acromegaly underwent: 1) hydrocortisone alone: a bolus iv injection of 100 mg hydrocortisone succinate in 2 mL saline, at time -60 followed by a 120 min iv infusion of 250 mg hydrocortisone succinate in 250 mL saline, from -60 to 60 min; 2) hexarelin+hydrocortisone: a bolus iv injection of hexarelin 100 micrograms, 60 min after initiation of a 2-hour hydrocortisone infusion; 3) hexarelin alone: a bolus iv injection of hexarelin at time 0, 60 min after initiation of a 2-hour saline infusion. The mean GH peak, expressed as percent change with respect to baseline level (mean of -75 and -60 minute samples), after hexarelin (1750 +/- 1157%) did not differ significantly with respect to that observed after hexarelin+hydrocortisone (1120 +/- 770%). After hydrocortisone alone the patients showed a mean decrease in GH levels as compared to baseline levels, of 47 +/- 7%. Our data show that the GH response to hexarelin in acromegaly is resistant to the inhibitor action of an acute and sustained elevation of serum cortisol levels. That hexarelin counteracts the glucocorticoid-mediated inhibition of GH secretion supports the hypothesis of an hexarelin-induced decrease in endogenous somatostatin tone.
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