A Sermorelin Injection Protocol details the prescribed schedule, dosage, and route of administration for Sermorelin Acetate, a synthetic GHRH analog, to stimulate the pulsatile release of endogenous Growth Hormone (GH) from the anterior pituitary gland. This protocol is clinically designed to enhance anabolic signaling, improve body composition, and support tissue repair by leveraging the body’s natural GH secretion mechanism. The injections are typically timed to coincide with the body’s natural nocturnal GH peak.
Origin
Sermorelin is derived from the first 29 amino acids of native Growth Hormone-Releasing Hormone (GHRH), placing its origin firmly within hypothalamic hormone research and peptide therapeutics. The “protocol” aspect emphasizes the structured, clinical application necessary to achieve physiological stimulation without receptor downregulation or adverse effects. It is a pharmaceutical strategy to support the somatotropic axis.
Mechanism
Sermorelin acts by binding to the GHRH receptor on the anterior pituitary somatotrophs, activating the adenylate cyclase system, which increases intracellular cAMP and calcium influx. This cascade results in the synthesis and secretion of stored GH into the systemic circulation. When administered subcutaneously, usually before sleep, it capitalizes on the natural pulsatile release pattern, leading to sustained, yet physiologic, elevations in circulating IGF-1. This elevated IGF-1 then mediates the desired anabolic and lipolytic effects throughout the body.
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