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Cited by 125Hormonal and reproductive studiesMuscle Physiology and DisordersNutrition and Health in Aging

The DOI matches its Crossref record; 71 of the 73 references it cites were found in a registry or an index.

Continuous testosterone administration prevents skeletal muscle atrophy and enhances resistance to fatigue in orchidectomized male mice

Axell, Anna-Maree, MacLean, Helen E., Plant, David R., Harcourt, Leah J., Davis, Jennifer A., Jimenez, Mark, Handelsman, David J., Lynch, Gordon S., Zajac, Jeffrey D.·2006·American Journal of Physiology-Endocrinology and Metabolism
DOI 10.1152/ajpendo.00058.2006
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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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Crossref · 10.1152/ajpendo.00058.2006

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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)
ORCID
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
DOI
10.1152/ajpendo.00058.2006
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

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