Human Type 3 5α-Reductase Is Expressed in Peripheral Tissues at Higher Levels Than Types 1 and 2 and Its Activity Is Potently Inhibited by Finasteride and Dutasteride

    Kazutoshi Yamana, Fernand Labrie, Van Luu-The
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    Finasteride →

    Frontline, gold standard treatment for combatting androgenic alopecia

    Dutasteride →

    Heavy duty finasteride that comes with higher risks

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    Studysummary This study found that SRD5a-3 is a highly efficient enzyme for converting hormones into androgens, with dutasteride being a much more potent inhibitor of SRD5a-3 than SRD5a-2.
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    This 12-year-old study found that human type 3 5α-reductase is expressed at higher levels than types 1 and 2 in peripheral tissues, and its activity is potently inhibited by finasteride and dutasteride. The enzyme may play an important role in androgen metabolism and could be a potential target for treating androgen-related disorders. The study used human tissues from various organs and included enzymatic assays to measure 5α-reductase activity.
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