The clinical application of Sermorelin, a synthetic peptide analog of Growth Hormone-Releasing Hormone (GHRH), to stimulate the pituitary gland’s pulsatile release of endogenous Growth Hormone (GH). Sermorelin Peptide Use is a therapeutic strategy aimed at correcting age-related or functional deficiencies in the GH-IGF-1 axis, often employed to improve body composition, enhance tissue repair, and support metabolic function. This approach utilizes the body’s own regulatory mechanisms rather than administering exogenous GH.
Origin
Sermorelin was developed based on the structure of the naturally occurring GHRH, which is secreted by the hypothalamus. Its clinical introduction provided a physiological means to boost GH levels, contrasting with the direct injection of recombinant human growth hormone. The “Peptide Use” designation underscores its role as a secretagogue, leveraging the body’s inherent feedback systems for a more natural release pattern.
Mechanism
As a GHRH analog, Sermorelin binds to the GHRH receptors on the somatotroph cells of the anterior pituitary gland. This binding triggers a second messenger cascade, primarily involving cyclic AMP, which stimulates the synthesis and release of GH in a pulsatile manner, mimicking the body’s natural rhythm. The released GH then acts on target tissues, stimulating the liver to produce Insulin-like Growth Factor 1 (IGF-1), which mediates most of the anabolic and growth-promoting effects.
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