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5α-reductase inhibitors

5α-Reductase inhibitor
Drug class
Dutasteride.svg
Dutasteride, one of the most widely used 5α-reductase inhibitors.
Class identifiers
Synonyms Dihydrotestosterone antagonists; Dihydrotestosterone blockers
Use Benign prostatic hyperplasia, androgenic alopecia, hirsutism, transgender women
ATC code G04CB
Biological target 5α-Reductase
Chemical class Azasteroids

5α-Reductase inhibitors (5-ARIs) are a class of drugs with anti-androgen effects, used primarily in the treatment of benign prostatic hyperplasia (BPH, enlarged prostate) and androgenic alopecia (pattern hair loss). They are also used less commonly to treat hirsutism (excessive hair growth) in women. These are two types of 5-ARIs, categorized as steroidal and non-steroidal 5α-recuctase inhibitors.

These agents inhibit the enzyme 5α-reductase, which is involved in the metabolic transformations of a variety of endogenous steroids. 5α-reductase inhibition is most known for preventing conversion of testosterone, the major androgen sex hormone, to the more potent dihydrotestosterone (DHT), in androgen-associated disorders.

5-ARIs are clinically used in the treatment of conditions that are exacerbated by DHT:

They have also been explored in the treatment and prevention of prostate cancer. While the 5-ARI finasteride reduces the cancer risk by about a third, it also increases the fraction of aggressive forms of prostate cancer. Overall, there does not seem to be a survival benefit for prostate cancer patients under finasteride.

5-ARIs can be used in the treatment of hirsutism in women.

5-ARIs are also sometimes employed as supplementary antiandrogens in hormone replacement therapy for trans women.


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