Intracrine and Myotrophic Roles of 5α-Reductase and Androgens

    Joshua F. Yarrow, Sean C. McCoy, Stephen E. Borst
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    Finasteride →

    Frontline, gold standard treatment for combatting androgenic alopecia

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    Heavy duty finasteride that comes with higher risks

    Studysummary This review discusses the role of skeletal muscle in synthesizing bioactive androgens, highlighting that intramuscular androgens may influence muscle via intracrine action, but their precise function remains unclear.
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    The document reviewed the roles of 5α-reductase and androgens in muscle development and maintenance, emphasizing that skeletal muscle can synthesize bioactive androgens like testosterone and DHT from DHEA, and that exercise increases the expression of androgen-biosynthesizing enzymes in muscle. It highlighted that testosterone increases muscle mass and strength dose-dependently, while DHT has a lesser effect despite its higher affinity for androgen receptors. The review discussed the impact of 5α-reductase inhibitors, noting that finasteride did not impede muscle development, but dutasteride did, suggesting a critical role for DHT in muscle growth. The potential of selective androgen receptor modulators (SARMs) to provide anabolic effects in muscle and bone while minimizing adverse effects in non-target tissues was also noted. The document concluded that further research is needed to understand the specific roles of 5α-reductase isozymes and locally produced androgens in muscle.
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