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Dual-5α-Reductase Inhibition Promotes Hepatic Lipid Accumulation in Man
Author(s) -
Jonathan Hazlehurst,
Andrei I. Oprescu,
Nikolaos Nikolaou,
Riccardo Di Guida,
Annabel Grinbergs,
Nigel P. Davies,
Robert Flintham,
Matthew J. Armstrong,
Angela E. Taylor,
Beverly Hughes,
Jinglei Yu,
Leanne Hodson,
Warwick B. Dunn,
Jeremy Tomlinson
Publication year - 2015
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2015-2928
Subject(s) - endocrinology , medicine , dyslipidemia , chemistry , dihydrotestosterone , lipid metabolism , dutasteride , metabolome , finasteride , adipose tissue , pharmacology , biology , metabolite , androgen , diabetes mellitus , prostate , cancer , hormone
5α-Reductase 1 and 2 (SRD5A1, SRD5A2) inactivate cortisol to 5α-dihydrocortisol in addition to their role in the generation of DHT. Dutasteride (dual SRD5A1 and SRD5A2 inhibitor) and finasteride (selective SRD5A2 inhibitor) are commonly prescribed, but their potential metabolic effects have only recently been identified.

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