Rapid actions of androgens
Abstract
The biological activity of androgens is thought to occur predominantly through binding to intracellular androgen-receptors, a member of the nuclear receptor family, that interact with specific nucleotide sequences to alter gene expression. This genomic-androgen effect typically takes at least more than half an hour. In contrast, the rapid or non-genomic actions of androgens are manifested within in seconds to few minutes. This rapid effect of androgens are manifold, ranging from activation of G-protein coupled membrane androgen-receptors or sex hormone-binding globulin receptors, stimulation of different protein kinases, to direct modulation of voltage- and ligand gated ion-channels and transporters. The physiological relevance of these non-genomic androgen actions has not yet been determined in detail. However, it may contribute to modulate several second messenger systems or transcription factors, which suggests a cross-talk between the fast non-genomic and the slow genomic pathway of androgens. This review will focus on the rapid effects of androgens on cell surface and cytoplasmic level.
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Androgen transmits signals via cell membrane receptors that are distinct from the androgen nuclear receptors.
“Androgen transmits signals via cell membrane receptors [19], which are distinct from the androgen nuclear receptors [20].”
From G protein-coupled receptors function as cell membrane receptors for the steroid hormone 20-hydroxyecdysone (2020) · cites this paper as [19]
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References 228 · Cited by 198
- Authors
- Michels, G., & Hoppe, U. C.
- Affiliations
- University of Cologne (DE)
- ORCID
- Hoppe, Uta C.
- Venue
- Frontiers in Neuroendocrinology
- Publisher
- Elsevier BV
- Published
- 2008-05
- Volume
- 29
- Issue
- 2
- Pages
- 182-198
- ISSN
- 0091-3022 (ISSN-L)
- OpenAlex
- W2011203985
- Cited by
- 198
- References
- 228
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 2 · 2023: 8 · 2022: 9 · 2021: 11 · 2020: 9 · 2019: 8 · 2018: 4 · 2017: 9 · 2016: 12 · 2015: 11 · 2014: 11 · 2013: 15 · 2012: 17
- FWCI
- 1.39
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Frontiers in Neuroendocrinology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Prostate Cancer Treatment and Research
- Keywords
- androgens, androgen receptor, G protein-coupled receptors, sex hormone-binding globulin, protein kinases, ion channels, second messengers, transcription factors
- MeSH terms
- Androgens, Animals, Calcium, Homeostasis, Humans, Ion Channels, Membrane Lipids, Models, Biological, Protein Kinase C, Receptors, Androgen, Sex Hormone-Binding Globulin, Testosterone, Time Factors, Transcription Factors, Second Messenger Systems, Ion Transport, Cyclic AMP-Dependent Protein Kinases, Phosphatidylinositol 3-Kinases, Mitogen-Activated Protein Kinases, Heterotrimeric GTP-Binding Proteins
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