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Continuous testosterone administration prevents skeletal muscle atrophy and enhances resistance to fatigue in orchidectomized male mice
Abstract
Androgens promote anabolism in skeletal muscle; however, effects on subsequent muscle function are less well defined because of a lack of reliable experimental models. We established a rigorous model of androgen withdrawal and administration in male mice and assessed androgen regulation of muscle mass, structure, and function. Adult C57Bl/6J male mice were orchidectomized (Orx) or sham-operated (Sham) and received 10 wk of continuous testosterone (T) or control treatment (C) via intraperitoneal implants. Mass, fiber cross-sectional area (CSA), and in vitro contractile function were assessed for fast-twitch extensor digitorum longus (EDL) and slow-twitch soleus (SOL) muscles. After 10 wk, Orx+C mice had reduced body weight gain ( P < 0.05), seminal vesicle mass ( P < 0.01), and levator ani muscle mass ( P < 0.001) compared with Sham+C mice, and these effects were prevented with testosterone treatment. Orx+T mice had greater EDL ( P < 0.01) and SOL ( P < 0.01) muscle mass compared with Orx+C mice; however, median fiber CSA was not significantly altered in these muscles. EDL and SOL muscle force was greater in Sham+T compared with Orx+C mice ( P < 0.05) in proportion to muscle mass. Unexpectedly, Orx+T mice had increased fatigue resistance of SOL muscle compared with Orx+C mice ( P < 0.001). We used a rigorous model of androgen withdrawal and administration in male mice to demonstrate an essential role of androgens in the maintenance of muscle mass and force. In addition, we showed that testosterone treatment increases resistance to fatigue of slow- but not fast-twitch muscle.
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“In mice, castration produces a decrease in body weight, which is attenuated with testosterone supplementation, and although overall muscle weight increases, the fiber CSA of the soleus and TA do not significantly change (6).”
From Sex-Based Differences in Skeletal Muscle Kinetics and Fiber-Type Composition (2015) · cites this paper as [6]
In the citing paper
“In mice, castration produces a decrease in body weight, which is attenuated with testosterone supplementation, and although overall muscle weight increases, the fiber CSA of the soleus and TA do not significantly change (6).”
From Sex-Based Differences in Skeletal Muscle Kinetics and Fiber-Type Composition (2015) · cites this paper as [6]
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Cites
The effects of supraphysiologic doses of testosterone on muscle size and strength in normal men
Bhasin, S., Storer, T. W., Berman, N., Callegari, C., Clevenger, B., Phillips, J., Bunnell, T. J., Tricker, R., Shirazi, A., & Casaburi, R. (1996) · New England Journal of Medicine · doi:10.1056/nejm199607043350101 · Cited by 1,659
Biological Actions of Androgens
MOORADIAN, A. D., MORLEY, J. E., & KORENMAN, S. G. (1987) · Endocrine Reviews · doi:10.1210/edrv-8-1-1 · Cited by 1,080
Testosterone dose-response relationships in healthy young men
Bhasin, S., Woodhouse, L., Casaburi, R., Singh, A. B., Bhasin, D., Berman, N., Chen, X., Yarasheski, K. E., Magliano, L., Dzekov, C., et al. (2001) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2001.281.6.e1172 · Cited by 967
Katznelson, L., Finkelstein, J. S., Schoenfeld, D. A., Rosenthal, D. I., Anderson, E. J., & Klibanski, A. (1996) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.81.12.8954042 · Cited by 791 · cited 1×
“Testosterone replacement therapy has been effectively used to counteract loss of lean body mass in hypogonadal men (4, 11, 32), older men with normal or low serum testosterone (21, 54), and HIV-infected men with low serum testosterone (2).”
BackgroundFiring patterns of motor units in normal rats
Hennig, R. O., & Lømo, T. (1985) · Nature · doi:10.1038/314164a0 · Cited by 725
Wang, C., Cunningham, G., Dobs, A., Iranmanesh, A., Matsumoto, A. M., Snyder, P. J., Weber, T., Berman, N., Hull, L., & Swerdloff, R. S. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-032006 · Cited by 656
Effects of Testosterone Replacement in Hypogonadal Men1
Snyder, P. J., Peachey, H., Berlin, J. A., Hannoush, P., Haddad, G., Dlewati, A., Santanna, J., Loh, L., Lenrow, D. A., Holmes, J. H., et al. (2000) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.85.8.6731 · Cited by 610
Testosterone Replacement Increases Fat-Free Mass and Muscle Size in Hypogonadal Men
Bhasin, S., Storer, T. W., Berman, N., Yarasheski, K. E., Clevenger, B., Phillips, J., Lee, W. P., Bunnell, T. J., & Casaburi, R. H. (1997) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.82.2.3733 · Cited by 596
Page, S. T., Amory, J. K., Bowman, F. D., Anawalt, B. D., Matsumoto, A. M., Bremner, W. J., & Tenover, J. L. (2005) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-1933 · Cited by 566
Singh, R., Artaza, J. N., Taylor, W. E., Gonzalez-Cadavid, N. F., & Bhasin, S. (2003) · Endocrinology · doi:10.1210/en.2003-0741 · Cited by 555
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Health State EstimationPreprint
Nag, N. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2003.09312 · Cited by 19
Pintana, H., Pongkan, W., Pratchayasakul, W., Chattipakorn, N., & Chattipakorn, S. C. (2015) · Journal of Endocrinology · doi:10.1530/joe-15-0099 · Cited by 16
Castration induces satellite cell activation that contributes to skeletal muscle maintenance
Klose, A. M., Liu, W., Paris, N. D., Forman, S., Krolewski, J. J., Nastiuk, K. L., & Chakkalakal, J. V. (2018) · JCSM Rapid Communications · doi:10.1002/j.2617-1619.2018.tb00004.x · Cited by 16
Selective Loss of Levator Ani and Leg Muscle Volumes in Men Undergoing Androgen Deprivation Therapy
Cheung, A. S., Cunningham, C., Ko, D., Ly, V., Gray, H. A., Hoermann, R., Strauss, B. J., Hassan, E. B., Duque, G., Ebeling, P. R., et al. (2018) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2018-01954 · Cited by 16
Self-citationNeto, W. K., Silva, W. D. A., Ciena, A. P., Bocalini, D. S., Nucci, R. A. B., Anaruma, C. A., & Gama, E. F. (2017) · The Aging Male · doi:10.1080/13685538.2017.1365832 · Cited by 16
Regulation of murine skeletal muscle growth by STAT5B is age- and sex-specific
Paul, R. G., Hennebry, A., Elston, M. S., Conaglen, J. V., & McMahon, C. D. (2019) · Skeletal Muscle · doi:10.1186/s13395-019-0204-3 · Cited by 17
McManus, J. F., Nguyen, N. N., Davey, R. A., MacLean, H. E., Pomilio, G., McCormack, M. P., Chiu, W. S. M., Wei, A. H., Zajac, J. D., & Curtis, D. J. (2020) · European Journal Of Haematology · doi:10.1111/ejh.13431 · Cited by 15
Self-citationLara‐García, M., Alvarado-Olivarez, M., Cuevas‐Romero, E., Cortés-Sol, A., Domínguez, A., Tovar, A., & Pacheco, P. (2011) · The Anatomical Record · doi:10.1002/ar.21414 · Cited by 14
miR-23b-3p acts as a counter-response against skeletal muscle atrophy
Okamura, T., Hashimoto, Y., Osaka, T., Senmaru, T., Fukuda, T., Hamaguchi, M., & Fukui, M. (2020) · Journal of Endocrinology · doi:10.1530/joe-19-0425 · Cited by 15
Transcriptomic profiling as a screening tool to detect trenbolone treatment in beef cattle
Pegolo, S., Cannizzo, F. T., BIOLATTI, B., Castagnaro, M., & Bargelloni, L. (2014) · Research in Veterinary Science · doi:10.1016/j.rvsc.2014.03.020 · Cited by 13
Clarke, M. V., Russell, P. K., Zajac, J. D., & Davey, R. A. (2019) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2019.02.018 · Cited by 13
Self-citationTranslational Strategies to Target Metastatic Bone Disease
Pagnotti, G. M., Trivedi, T., & Mohammad, K. S. (2022) · Cells · doi:10.3390/cells11081309 · Cited by 13
Sinnesael, M., Callewaert, F., Morreels, M., Kumar, N., Sitruk-Ware, R. L., Proeyen, K. V., Hespel, P., Boonen, S., Claessens, F., & Vanderschueren, D. (2011) · International Journal of Andrology · doi:10.1111/j.1365-2605.2011.01198.x · Cited by 11
Ung, R., Rouleau, P., & Guertin, P. A. (2010) · Journal of Neurotrauma · doi:10.1089/neu.2009.1211 · Cited by 12
Cypriano, M. L., Ramos, G. H. A. D. S., de Oliveira, A. C. F., dos Santos, D. R., Fiais, G. A., de Oliveira, A. P., Antoniali, C., Dornelles, R. C. M., Nakamune, A. C. D. M. S., & Chaves-Neto, A. H. (2021) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2021.105289 · Cited by 11
Chronological Molecular Changes in Neuronal Communication in Androgen-Deficient Rats
Fainanta, T., Jaroenporn, S., Wititsuwankul, P., & Malaivijitnond, S. (2019) · Journal of Molecular Neuroscience · doi:10.1007/s12031-019-01335-7 · Cited by 11
Toxic effects of methyl methacrylate monomer on male genital tissues. In vitro study in rats.
Fakhouri, J., Sarkis, R., Chababi‐Atallah, M., & Aftimos, G. (2008) · PubMed · Cited by 11
Guo, K. X., Zhu, J., Quan, X., Zhang, D., Chen, X., Yang, C., Li, X., Shi, J., Hu, W., & Zhu, Q. (2015) · Acupuncture in Medicine · doi:10.1136/acupmed-2014-010686 · Cited by 10
Influence of gonadectomy on muscle health in micro- and partial-gravity environments in rats
Rosa‐Caldwell, M. E., Mortreux, M., Wadhwa, A., Kaiser, U. B., Sung, D., Bouxsein, M., & Rutkove, S. B. (2023) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00023.2023 · Cited by 9
de Souza, T. P., Yamada, A. K., Junior, R. F. S., Polotow, T. G., Curi, R., Pope, Z. K., Willardson, J. M., & Barros, M. P. (2012) · European Journal of Applied Physiology · doi:10.1007/s00421-012-2538-y · Cited by 7
mTORC1 in the Control of Myogenesis and Adult Skeletal Muscle Mass
Wallace, M. A., Hughes, D. C., & Baar, K. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802733-2.00025-6 · Cited by 9
Sabbouri, H. E. K. E., Hallal, N., Darwiche, W., Gay‐Queheillard, J., Bach, V., Ramadan, W., & Joumaa, W. H. (2022) · Toxicology and Environmental Health Sciences · doi:10.1007/s13530-021-00121-6 · Cited by 6
Effects of tail suspension on serum testosterone and molecular targets regulating muscle mass
Naeyer, H. D., Lamon, S., Russell, A. P., Everaert, I., Spaey, A. D., Jamart, C., Vanheel, B., Taes, Y., & Derave, W. (2014) · Muscle & Nerve · doi:10.1002/mus.24542 · Cited by 6
The Effect of Severe Androgen Deficiency on Physical Function in Male Patients With Cancer
Gagnon, B., Murphy, J., Jelowicki, M., & Morris, D. V. (2012) · Journal of Pain and Symptom Management · doi:10.1016/j.jpainsymman.2012.05.010 · Cited by 6
Żylicz, Z. (2009) · Via Medica Journals · Cited by 5
Metadata
- Authors
- Axell, A.-M., MacLean, H. E., Plant, D. R., Harcourt, L. J., Davis, J. A., Jimenez, M., Handelsman, D. J., Lynch, G. S., & Zajac, J. D.
- Affiliations
- The University of Melbourne (AU)
- Venue
- American Journal of Physiology-Endocrinology and Metabolism
- Publisher
- American Physiological Society
- Published
- 2006-09
- Volume
- 291
- Issue
- 3
- Pages
- E506-E516
- ISSN
- 0193-1849 (ISSN-L)
- 1522-1555
- OpenAlex
- W2119647215
- Cited by
- 125
- References
- 73
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 3 · 2023: 6 · 2022: 4 · 2021: 6 · 2020: 7 · 2019: 6 · 2018: 6 · 2017: 7 · 2016: 9 · 2015: 9 · 2014: 7 · 2013: 4 · 2012: 11
- FWCI
- 2.94
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Physiology (medical) › Nutrition and Health in Aging
- Keywords
- testosterone, androgens, skeletal muscle atrophy, androgen withdrawal, orchiectomy, muscle fatigue resistance, muscle mass, muscle fiber cross-sectional area, slow-twitch muscle, fast-twitch muscle, extensor digitorum longus, soleus muscle, muscle force, male mice
- MeSH terms
- Animals, Body Weight, Male, Mice, Inbred C57BL, Muscle Contraction, Muscular Atrophy, Orchiectomy, Seminal Vesicles, Testis, Testosterone, Muscle, Skeletal, Muscle Fibers, Fast-Twitch, Muscle Fibers, Slow-Twitch, Muscle Fatigue, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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