Study summary · research use only
Ipamorelin, the first selective growth hormone secretagogue
Plain-language summary
Paraphrased from the published abstract below — not a verdict on whether anything works.
This study describes ipamorelin, a pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH2) GH secretagogue, characterized in vitro and in vivo. The abstract reports ipamorelin released GH from primary rat pituitary cells with potency and maximal effect similar to GHRP-6 (EC50 1.3+/-0.4 nmol/l, Emax 85+/-5% vs 2.2+/-0.3 nmol/l and 100%), and antagonist profiling indicated it acts via a GHRP-like receptor. In anaesthetized rats, ipamorelin released GH comparably to GHRP-6 (ED50 80+/-42 nmol/kg), and in conscious swine with ED50 2.3+/-0.03 nmol/kg. In swine, none of the secretagogues affected FSH, LH, PRL or TSH; GHRP-6 and GHRP-2 raised ACTH and cortisol, whereas ipamorelin did not raise these even at doses more than 200-fold higher than the GH ED50. The authors describe ipamorelin as selective for GH release.
Abstract
The development and pharmacology of a new potent growth hormone (GH) secretagogue, ipamorelin, is described. Ipamorelin is a pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH2), which displays high GH releasing potency and efficacy in vitro and in vivo. As an outcome of a major chemistry programme, ipamorelin was identified within a series of compounds lacking the central dipeptide Ala-Trp of growth hormone-releasing peptide (GHRP)-1. In vitro, ipamorelin released GH from primary rat pituitary cells with a potency and efficacy similar to GHRP-6 (ECs) = 1.3+/-0.4nmol/l and Emax = 85+/-5% vs 2.2+/-0.3nmol/l and 100%). A pharmacological profiling using GHRP and growth hormone-releasing hormone (GHRH) antagonists clearly demonstrated that ipamorelin, like GHRP-6, stimulates GH release via a GHRP-like receptor. In pentobarbital anaesthetised rats, ipamorelin released GH with a potency and efficacy comparable to GHRP-6 (ED50 = 80+/-42nmol/kg and Emax = 1545+/-250ng GH/ml vs 115+/-36nmol/kg and 1167+/-120ng GH/ml). In conscious swine, ipamorelin released GH with an ED50 = 2.3+/-0.03 nmol/kg and an Emax = 65+/-0.2 ng GH/ml plasma. Again, this was very similar to GHRP-6 (ED50 = 3.9+/-1.4 nmol/kg and Emax = 74+/-7ng GH/ml plasma). GHRP-2 displayed higher potency but lower efficacy (ED50 = 0.6 nmol/kg and Emax = 56+/-6 ng GH/ml plasma). The specificity for GH release was studied in swine. None of the GH secretagogues tested affected FSH, LH, PRL or TSH plasma levels. Administration of both GHRP-6 and GHRP-2 resulted in increased plasma levels of ACTH and cortisol. Very surprisingly, ipamorelin did not release ACTH or cortisol in levels significantly different from those observed following GHRH stimulation. This lack of effect on ACTH and cortisol plasma levels was evident even at doses more than 200-fold higher than the ED50 for GH release. In conclusion, ipamorelin is the first GHRP-receptor agonist with a selectivity for GH release similar to that displayed by GHRH. The specificity of ipamorelin makes this compound a very interesting candidate for future clinical development.
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