Ipamorelin Science refers to the clinical and pharmacological study of Ipamorelin, a synthetic pentapeptide that functions as a highly selective growth hormone secretagogue (GHS). This compound specifically mimics the action of ghrelin, the endogenous ligand for the Growth Hormone Secretagogue Receptor (GHSR), stimulating the pituitary gland to release Growth Hormone (GH). Its clinical utility lies in its ability to induce a natural, pulsatile release of GH without significantly impacting cortisol, prolactin, or ACTH levels.
Origin
Ipamorelin was developed in the late 20th century as part of research efforts to create potent, orally active, and highly specific secretagogues for the therapeutic management of Growth Hormone Deficiency. The Science component denotes the ongoing research into its efficacy, safety profile, and applications in body composition, tissue repair, and hormonal health.
Mechanism
Ipamorelin works by binding with high affinity to the GHSR, primarily located in the pituitary gland and hypothalamus. This binding activates the receptor, leading to a robust and natural pulsatile release of GH from the somatotroph cells of the anterior pituitary. Critically, its unique structure minimizes the stimulation of other pituitary hormones, offering a cleaner pharmacological profile compared to earlier GHS compounds.
We use cookies to personalize content and marketing, and to analyze our traffic. This helps us maintain the quality of our free resources. manage your preferences below.
Detailed Cookie Preferences
This helps support our free resources through personalized marketing efforts and promotions.
Analytics cookies help us understand how visitors interact with our website, improving user experience and website performance.
Personalization cookies enable us to customize the content and features of our site based on your interactions, offering a more tailored experience.