Cited by 57Sexual Differentiation and DisordersHormonal and reproductive studiesProstate Cancer Treatment and Research

5α-Reductases in human physiology: an unfolding story

Traish, Abdulmaged M.·2012·Endocrine Practice

Abstract

Objective 5α-reductases are a family of isozymes expressed in a wide host of tissues including the central nervous system (CNS) and play a pivotal role in male sexual differentiation, development and physiology.Methods A comprehensive literature search from 1970 to 2011 was made through PubMed and the relevant information was summarized.Results 5α reductases convert testosterone, progesterone, deoxycorticosterone, aldosterone and corticosterone into their respective 5α-dihydro-derivatives, which serve as substrates for 3α-hydroxysteroid dehydrogenase enzymes. The latter transforms these 5α-reduced metabolites into a subclass of neuroactive steroid hormones with distinct physiological functions. The neuroactive steroid hormones modulate a multitude of functions in human physiology encompassing regulation of sexual differentiation, neuroprotection, memory enhancement, anxiety, sleep and stress, among others. In addition, 5α -reductase type 3 is also implicated in the N-glycosylation of proteins via formation of dolichol phosphate. The family of 5α-reductases was targeted for drug development to treat pathophysiological conditions, such as benign prostatic hyperplasia and androgenetic alopecia. While the clinical use of 5α-reductase inhibitors was well established, the scope and the magnitude of the adverse side effects of such drugs, especially on the CNS, is still unrecognized due to lack of knowledge of the various physiological functions of this family of enzymes, especially in the CNS.Conclusion There is an urgent need to better understand the function of 5α-reductases and the role of neuroactive steroids in human physiology in order to minimize the potential adverse side effects of inhibitors targeting 5α-reductases to treat benign prostatic hyperplasia and androgenic alopecia.

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Crossref · 10.4158/ep12108.ra

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  • In liver and some peripheral tissues such as placenta and myometrium, AKR1D1 reduces progesterone to 5β-DHP, while SRD5A1 and SRD5A2 form 5α-DHP.

    “In liver and some peripheral tissues (e.g. placenta and myometrium) AKR1D1 catalyzes reduction of progesterone to 5β-dihydroprogesterone (5β-DHP) while the 5α-reductases SRD5A1 and SRD5A2 form 5α-dihydroprogesterone (5α-DHP)”

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References 109 · Cited by 57

Authors
Traish, A. M.
Affiliations
Boston University (US)
Corresponding author
Traish, Abdulmaged M.
Venue
Endocrine Practice
Publisher
Elsevier BV
Published
2012-11
Volume
18
Issue
6
Pages
965-975
ISSN
1530-891X (ISSN-L)
OpenAlex
W2078924933
Cited by
57
References
109
Citations by year
2026: 3 · 2025: 7 · 2024: 1 · 2023: 2 · 2022: 2 · 2021: 3 · 2020: 4 · 2019: 1 · 2018: 7 · 2017: 5 · 2016: 2 · 2015: 6 · 2014: 9 · 2013: 4
FWCI
2.44
Type
journal article
Language
en
Open access
closed
Locations
  • Endocrine Practice (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Prostate Cancer Treatment and Research
Keywords
5α-reductase, neurosteroids, 3α-hydroxysteroid dehydrogenase, male sexual differentiation, central nervous system, neuroprotection, memory enhancement, anxiety, sleep, stress, N-glycosylation, dolichol phosphate, 5-alpha reductase inhibitors, benign prostatic hyperplasia, androgenetic alopecia
MeSH terms
Alopecia, Animals, Central Nervous System, Enzyme Inhibitors, Female, Humans, Isoenzymes, Male, Memory, Prostatic Hyperplasia, Sex Differentiation, Mice, Knockout, Models, Animal, Cholestenone 5 alpha-Reductase, Mice

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