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Key findings: Ipamorelin produced dose-dependent GH release comparable to GHRP-6 Unlike GHRP-6, ipamorelin did not stimulate ACTH or cortisol release, even at doses up to 200 times higher than the effective GH-releasing dose Ipamorelin did not significantly increase prolactin levels The GH response was specific and consistent, supporting its classification as the most selective GHRP identified at the time This study established the foundation for all subsequent ipamorelin research and remains one of the most frequently cited papers in the field

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Reactive sulfur species-mediated activation of the Keap1-Nrf2 pathway by 1,2-naphthoquinone through sulfenic acids formation under oxidative stress