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Gonadotropin-releasing hormone agonist

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Title: Gonadotropin-releasing hormone agonist  
Author: World Heritage Encyclopedia
Language: English
Subject: Assisted reproductive technology, Danazol, Cyanoketone, Hormone replacement therapy, Cyproterone acetate
Collection: Antiandrogens, Antiestrogens, Antigonadotropins, Fertility Medicine, Gonadotropin-Releasing Hormone and Gonadotropins, Hormonal Agents
Publisher: World Heritage Encyclopedia

Gonadotropin-releasing hormone agonist

A gonadotropin-releasing hormone agonist (GnRH agonist, GnRH–A) is a synthetic peptide modeled after the hypothalamic neurohormone GnRH that interacts with the gonadotropin-releasing hormone receptor to elicit its biologic response, the release of the pituitary hormones FSH and LH.

GnRH agonists are pregnancy category X drugs.


  • Medical uses 1
  • Side effects 2
  • Flare effect and downregulation 3
  • Agonists with double and single substitutions 4
  • Administration 5
  • See also 6
  • External links 7
  • References 8

Medical uses

GnRH agonists are useful in:

Women of reproductive age who undergo cytotoxic chemotherapy have been pretreated with GnRH agonists to reduce the risk of oocyte loss during such therapy and preserve ovarian function. Further studies are necessary to prove that this approach is useful.

Side effects

Side effects of the GnRH agonists are signs and symptoms of hypoestrogenism, including hot flushes, headaches, and osteoporosis. In patients under long-term therapy, small amounts of estrogens could be given back (“add-back regimen”) to combat such side effects and to prevent bone wastage. Generally, long-term patients, both male and female, tend to undergo annual DEXA scans to appraise bone density.

There is also a report that GnRH agonists used in the treatment of advanced prostate cancer may increase the risk of heart problems by 30%.[2]

Flare effect and downregulation

Agonists do not quickly dissociate from the GnRH receptor. As a result initially there is an increase in FSH and LH secretion (so-called "flare effect").

However after about ten days, a profound hypogonadal effect (i.e. decrease in FSH and LH) is achieved through receptor downregulation by internalization of receptors. Generally this induced and reversible hypogonadism is the therapeutic goal.

Agonists with double and single substitutions

GnRH agonists are synthetically modeled after the natural GnRH decapeptide with specific modifications, typically in position 6 (amino acid substitution), 9 (alkylation) and 10 (deletion). These substitutions inhibit rapid degradation. Agonists with two substitutions include: leuprolide (Lupron, Eligard), buserelin (Suprefact, Suprecor), histrelin (Supprelin LA, Vantas), goserelin (Zoladex), and deslorelin (Suprelorin, Ovuplant). The agents nafarelin (Synarel) and triptorelin are agonists with single substitutions at position 6.


These medications can be administered intranasally, by injection, or by implant. Injectables have been formulated for daily, monthly, and quarterly use; and implants can last from 1 to 12 months.

See also

External links

  • Buserelin website
  • Use of agonists in endometriosis
  • Lupron, by manufacturer
  • Lupron victims hub, website against use of this drug.
  • 10th International Symposium on GnRH
  • SupprelinLA, by Endo Pharmaceuticals, Inc.
  • Information of use of Zoladex in prostate cancer


  1. ^ van Loenen AC, Huirne JA, Schats R, Hompes PG, Lambalk CB (November 2002). "GnRH agonists, antagonists, and assisted conception". Semin. Reprod. Med. 20 (4): 349–64.  
  2. ^ "Researchers Suggest Hormone Therapy for Prostate Cancer Can Cause Serious Heart Problems and Death"

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