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how might buserelin acetate treat androgenetic alopecia ?

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How might buserelin acetate treat androgenetic alopecia

Buserelin acetate is the generic name for the commercial brand name Suprefact. It comes in two forms as an intranasal spray: 100 mcg/spray (100 sprays/bottle), or depot for skin (sub cutaneous) injection: 1 mg/mL (multidose vial).

Buserelin acetate is a synthetic drug that has the equivalent properties of natural gonadotropin-releasing hormone (GnRH/LHRH) that we all produce in our bodies. However, buserelin acetate is far more powerful than the natural hormone. Buserelin acetate promotes follicle stimulating hormone (FSH) and luteinizing hormone (LH) release 20 to 170 times greater than observed with LHRH. Long term use of buserelin acetate suppresses production of steroid hormones and gonadotrophin. Consequently, there is a reduction in steroid hormone levels such as testosterone in the blood.

It is most frequently used to treat prostate cancer, but may also have potential for treating pattern baldness. Only a few studies examine buserelin acetate use for androgen dependant diseases other than prostate cancer and none look at using it for pattern baldness treatment. However, one study looked at the use of oral buserelin acetate for hirsutism in women. The results were favorable.


How might buserelin acetate treat androgenetic alopecia references

  • Bertoli A, Fusco A, Magnani A, Marini MA, Di Daniele N, Gatti S, Lauro R. Efficacy of low-dose GnRH analogue (Buserelin) in the treatment of hirsutism. Exp Clin Endocrinol Diabetes. 1995;103(1):15-20.
  • Faloia E, Filipponi S, Mancini V, Morosini P, De Pirro R. Treatment with a gonadotropin-releasing hormone agonist in acne or idiopathic hirsutism. J Endocrinol Invest. 1993 Oct;16(9):675-7.
  • Urbancsek J, Rabe T, Gor U, Schulte B, Grunwald K, Papp Z, Runnebaum B. Effect of the GnRH analog buserelin on sex hormone serum level in relation to treatment onset and duration. Geburtshilfe Frauenheilkd. 1991 Aug;51(8):617-25.
  • Faure N, Lemay A. Ovarian suppression in polycystic ovarian disease during 6 month administration of a luteinizing hormone-releasing hormone (LH-RH) agonist. Clin Endocrinol (Oxf). 1987 Dec;27(6):703-13.

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