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Peptide Library / Detail
Half-life
Sustained release over 6-12 months from implant formulation
Delivery
Subcutaneous implant (slow-release formulation)
Dosage
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Research Use Only
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Deslorelin is a synthetic gonadotropin-releasing hormone (GnRH) agonist peptide used primarily in veterinary medicine for reproductive control and hormonal manipulation. It works by initially stimulating and then suppressing the hypothalamic-pituitary-gonadal axis, leading to reversible suppression of reproductive function. The peptide is commonly administered as a slow-release subcutaneous implant for temporary contraception and management of hormone-dependent conditions in various animal species.
Typically administered as subcutaneous implants in doses ranging from 4.7 mg to 9.4 mg depending on species and body weight. In dogs, 4.7 mg implants are standard for males and females. In cats (queens), 9.4 mg implants are used. Duration of effect varies by species: approximately 6-12 months in dogs, with suppression beginning 4-6 weeks post-implantation. Implant location can affect efficacy, with interscapular placement commonly used.
Deslorelin acts as a potent GnRH agonist that initially causes a surge in follicle-stimulating hormone (FSH) and luteinizing hormone (LH), followed by receptor desensitization and downregulation of the pituitary-gonadal axis. This results in decreased testosterone production in males and suppression of estrous cycles in females. The peptide influences androgen receptor expression and prostaglandin metabolism in reproductive tissues, leading to reversible suppression of spermatogenesis, testicular function, and ovarian activity (PMID: 41349370). In females, it can also be used at lower doses to induce ovulation before suppression occurs.