Androgen-mediated regulation of skeletal muscle protein balance
Open accessAbstract
Androgens significantly alter muscle mass in part by shifting protein balance in favor of net protein accretion. During various atrophic conditions, the clinical impact of decreased production or bioavailability of androgens (termed hypogonadism) is important as a loss of muscle mass is intimately linked with survival outcome. While androgen replacement therapy increases muscle mass in part by restoring protein balance, this is not a comprehensive treatment option due to potential side effects. Therefore, an understanding of the mechanisms by which androgens alter protein balance is needed for the development of androgen-independent therapies. While the data in humans suggest androgens alter protein balance (both synthesis and breakdown) in the fasted metabolic state, a predominant molecular mechanism(s) behind this observation is still lacking. This failure is likely due in part to inconsistent experimental design between studies including failure to control nutrient/feeding status, the method of altering androgens, and the model systems utilized.
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Testosterone plays a crucial role in increasing protein synthesis and inhibiting muscle proteolysis in skeletal muscle.
“As a principal anabolic hormone, testosterone plays a crucial role in increasing protein synthesis and inhibiting muscle proteolysis in skeletal muscle (140, 141).”
From From mitochondria to sarcopenia: role of 17β-estradiol and testosterone (2023) · cites this paper as [140]
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References 89 · Cited by 95
Research works printed but not linked: 1
- Milan G Romanello V Pescatore F Armani A Paik JH Frasson L Seydel A Zhao JH Abraham R Goldberg AL Blaauw B DePinho RA Sandri M 2015 Regulation of autophagy and the ubiquitin-proteasome system by the FoxO transcriptional network during muscle atrophy Nat Commun 6 PMC4403316 25858807
- Authors
- Rossetti, M. L., Steiner, J. L., & Gordon, B. S.
- Affiliations
- University of Central Florida (US)
- Pennsylvania State University (US)
- Corresponding author
- Gordon, Bradley S.
- Venue
- Molecular and Cellular Endocrinology
- Publisher
- Elsevier BV
- Published
- 2017-05
- Volume
- 447
- Pages
- 35-44
- ISSN
- 0303-7207 (ISSN-L)
- PMC
- PMC5407187
- OpenAlex
- W2590733966
- Cited by
- 95
- References
- 89
- Citations by year
- 2026: 5 · 2025: 12 · 2024: 8 · 2023: 17 · 2022: 12 · 2021: 5 · 2020: 5 · 2019: 15 · 2018: 11 · 2017: 4 · 2016: 1
- FWCI
- 1.12
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular and Cellular Endocrinology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Journal of International Crisis and Risk Communication Research (submittedVersion)
- Funders
- National Institute on Alcohol Abuse and Alcoholism (F32AA023422)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Keywords
- androgens, skeletal muscle, protein balance, muscle mass, hypogonadism, testosterone replacement therapy, muscle atrophy, protein synthesis, protein degradation
- MeSH terms
- Androgens, Animals, Humans, Models, Biological, Muscle Proteins, Protein Biosynthesis, Muscle, Skeletal, Proteolysis
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