5α-Reductases in human physiology: an unfolding story
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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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)”
From Role of aldo-keto reductase family 1 (AKR1) enzymes in human steroid metabolism (2014) · cites this paper as [38]
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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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