— peptide / growth —
Selective pentapeptide ghrelin receptor agonist investigated as a growth hormone secretagogue with minimal effects on cortisol and prolactin.
Raun et al. Eur J Endocrinol 1998. Novo Nordisk research. Clean selectivity profile vs other ghrelin agonists. Read more →
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Research-grade material. Documentation summarizes published literature in third-person scientific context. Not medical advice; not for human consumption.
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— The literature —
Ipamorelin binds the growth hormone secretagogue receptor type 1a (GHSR-1a), a class A G-protein coupled receptor expressed on pituitary somatotrophs, hypothalamic arcuate nucleus neurons, and several peripheral tissues. Receptor activation couples primarily through Gq to phospholipase C-beta, generating inositol trisphosphate and mobilizing intracellular calcium. This calcium signal triggers exocytosis of stored growth hormone from somatotroph secretory granules.
The selective profile of ipamorelin compared with earlier GHRPs has been attributed to the specific conformational presentation of the pentapeptide at the GHSR-1a binding pocket, with reduced engagement of alternative signaling pathways or off-target receptors implicated in cortisol and prolactin release. When combined with GHRH receptor agonists such as sermorelin or modified GRF (1-29), ipamorelin produces synergistic growth hormone release, reflecting the complementary Gs and Gq signaling pathways activated by the two receptor systems in somatotrophs.
All compounds discussed are intended for research use only. Not for human consumption. Research-context information is educational and does not constitute medical advice.
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