— peptide / growth —
Synthetic hexapeptide ghrelin receptor agonist investigated for potent growth hormone-releasing activity with characterized cortisol and prolactin effects.
Bowers et al. 1980s-90s. Pralmorelin (Japanese diagnostic agent) clinical reports. 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 —
GHRP-2 binds the growth hormone secretagogue receptor type 1a (GHSR-1a) on pituitary somatotrophs, activating Gq-mediated phospholipase C signaling, elevating intracellular calcium, and triggering exocytosis of stored growth hormone. The hexapeptide also engages central nervous system GHSR-1a, contributing to the appetite-stimulating effects observed in preclinical models and to modest activation of the hypothalamic-pituitary-adrenal axis.
Mechanistic comparisons with ipamorelin have attributed the greater cortisol and prolactin response of GHRP-2 to broader engagement of central neuropeptide systems and possibly to activity at additional receptors beyond GHSR-1a. The downstream cortisol elevation appears to result from activation of corticotropin-releasing hormone neurons in the paraventricular nucleus rather than direct adrenocortical stimulation. Prolactin release likely reflects engagement of lactotrophs through indirect hypothalamic mechanisms.
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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