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Dutasteride


Mechanism of action:

Dutasteride is an antiandrogenic agent that inhibits 5-alpha reductase. In humans, there are two major 5-alpha reductase isoenzymes: type I is distributed in the skin, liver, and sebaceous glands of the scalp, while type II is found in the prostate, seminal vesicles, hair follicles, and genital tissues. Dutasteride inhibits both type I and type II enzymes, thereby suppressing the synthesis of dihydrotestosterone (DHT), reducing DHT-mediated stimulation and proliferative signaling in prostatic tissue, and influencing physiological features associated with lower urinary tract obstruction.

Reference(s):

1. Keam SJ et al. (2008). Dutasteride: a review of its use in the management of prostate disorders. Drugs. 


2. Shah SK et al. (2009). Phase II study of dutasteride for recurrent prostate cancer during androgen deprivation therapy. J Urol. 


3. Arif T et al. (2017). Dutasteride in androgenetic alopecia: an update. Curr Clin Pharmacol.

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