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Nafarelin


Mechanism of action:

Nafarelin is a gonadotropin-releasing hormone analog. In the initial phase, nafarelin continuously stimulates gonadotropin-releasing hormone receptors in the anterior pituitary, causing a transient rise in luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which temporarily increases sex hormone levels such as testosterone or estrogen. With continued administration, gonadotropin-releasing hormone receptors become desensitized and downregulated due to prolonged stimulation, markedly weakening pituitary responsiveness to gonadotropin-releasing hormone. As a result, luteinizing hormone and follicle-stimulating hormone begin to decrease, leading to reduced sex hormone production.

Reference(s):

1. Hugues JN et al. (1998). Revisiting gonadotrophin-releasing hormone agonist protocols and management of poor ovarian responses to gonadotrophins. Hum Reprod Update. 


2. Garner C et al. (1994). Uses of GnRH agonists. J Obstet Gynecol Neonatal Nurs. 


3. Henzl MR et al. (1992). Gonadotropin-releasing hormone analogs: update on new findings. Am J Obstet Gynecol.

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