Biological Actions of Androgens
Abstract
Though unnecessary for life itself, androgens are essential for the propagation of the species and for establishment and maintenance of the quality of life of males through their support of sexual behavior and function, muscle strength, and sense of well-being. In carrying out its many functions, T acts both as hormone and prohormone. It is an outstanding example of the diverse evolutionary utilization of a primitive informational molecule both among and within species. Not only does T act through the androgen receptor both unchanged and via 5 alpha-reduction, but it acts in tissues with a high aromatase level as an estrogen via the estrogen receptor. Furthermore, DHT, binding to the estrogen receptor, can act as an inhibitor of estrogen action. The products of androgen metabolism may also play active regulatory roles in hematopoiesis and in the regulation of certain hepatic enzymes. Table 3 summarizes the actions of secreted T in males indicating the probable effector hormone. While gross hypogonadism is uncommon, mild androgen insufficiency may be much more frequent, especially in older men, and in those receiving treatment for chronic medical conditions. It is quite possible that such individuals would benefit from appropriate androgen therapy were it available, but the current forms of replacement therapy are not very satisfactory. Better approaches are required. With the exception of a small number of secreted proteins, the products of transcription induced by androgens are not, as yet, known. When the androgen receptor gene is cloned it will be possible to identify androgen-regulated genes and their products. It will then be possible to design agents selectively producing specific desired androgenic effects.
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Testosterone is a highly studied androgen that is associated with an increase in muscle mass.
“Testosterone is a highly studied androgen that is associated with an increase in muscle mass (66, 83).”
From Sex-Based Differences in Skeletal Muscle Kinetics and Fiber-Type Composition (2015) · cites this paper as [66]
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- Authors
- MOORADIAN, A. D., MORLEY, J. E., & KORENMAN, S. G.
- Affiliations
- United States Department of Veterans Affairs (US)
- Corresponding author
- KORENMAN, S. G.
- ORCID
- MORLEY, J. E.
- Venue
- Endocrine Reviews
- Publisher
- The Endocrine Society
- Published
- 1987-02
- Volume
- 8
- Issue
- 1
- Pages
- 1-28
- ISSN
- 0163-769X (ISSN-L)
- 1945-7189
- OpenAlex
- W2027586930
- Cited by
- 1,080
- References
- 3
- Citations by year
- 2026: 10 · 2025: 7 · 2024: 19 · 2023: 27 · 2022: 27 · 2021: 41 · 2020: 41 · 2019: 26 · 2018: 31 · 2017: 35 · 2016: 40 · 2015: 29 · 2014: 29 · 2013: 33 · 2012: 39
- FWCI
- 16.17
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrine Reviews (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Prostate Cancer Treatment and Research
- Keywords
- androgens, testosterone, dihydrotestosterone, androgen receptor, aromatase, estrogen receptor, 5α-reduction, androgen metabolism, hematopoiesis, hepatic enzyme regulation, androgen deficiency, testosterone replacement therapy, androgen-regulated genes, male sexual function, muscle strength
- MeSH terms
- Androgens, Animals, Brain, Breast, Genitalia, Male, Heart, Hematopoiesis, Humans, Hypothalamo-Hypophyseal System, Immune System, Kidney, Libido, Male, Mammary Glands, Animal, Sexual Behavior, Animal, Sex Characteristics, Testis, Muscle Development
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