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In Tiermodellen wirkt Ipamorelin als selektiver Agonist am GHS-R1a-Rezeptor (Ghrelin-Rezeptor) und löst eine pulsatile Wachstumshormon-Freisetzung aus, ohne die Cortisol- oder Prolaktinspiegel signifikant zu erhöhen — diese Selektivität unterscheidet es in der Literatur von älteren GHRPs wie GHRP-6 oder GHRP-2

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