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Updated: Jul 2, 2025

Skeletal Muscle Gender Dimorphism from Proteomics
Published on: December 14, 2011
Early Life Androgen Administration Attenuates Aging Related Declines in Muscle Protein Synthesis
David D Church1, Amit Zamir2, Guillermo Escalante3
1Donald W. Reynolds Institute on Aging, Center for Translational Research in Aging & Longevity, University of Arkansas for Medical Sciences, Little Rock, AR.
Purpose:
This study examined the acute and long-term effects of nandrolone decanoate (ND) on fractional synthetic rates (FSR).
Methods:
Male C57BL/6 mice were randomized into ND ( n = 20) or sham ( n = 20) groups. ND injections (10 g·kg -1 ·wk -1 ) started at 7 months of ages and continued for 6 wk. Ten animals from each group were randomly separated and examined 1 wk following drug cessation. The remaining animals were examined at 16 months of age. Animals were injected IP with 1.5 mL of deuterated water 24 h before euthanasia. The kidney, liver, heart, gastrocnemius, and soleus were extracted. Samples were analyzed for deuterated alanine enrichment in the bound protein and intracellular fraction by liquid chromatography tandem mass spectrometry to measure estimated FSR (fraction/day (F/D)) of mixed tissue.
Results:
One-way ANOVA, with treatment and age as fixed factors, indicated that kidney FSR was greater ( P = 0.027) in ND (0.41 ± 0.02 F/D) than sham (0.36 ± 0.014F/D) and higher ( P = 0.003) in young (0.42 ± 0.2 F/D) than old (0.35 ± 0.01 F/D). Liver and heart FSR values were greater ( P ≤ 0.001) in young (0.79 ± 0.06 F/D and 0.13 ± 0.01 F/D, respectively) compared with old (0.40 ± 0.01 F/D and 0.09 ± 0.01 F/D, respectively), but not between ND and sham. Gastrocnemius FSR was ( P ≤ 0.001) greater in young (0.06 ± 0.01 F/D) compared with old (0.03 ± 0.002 F/D), and greater ( P = 0.006) in ND (0.05 ± 0.01 F/D) compared with sham (0.04 ± 0.003 F/D). Soleus FSR rates were greater ( P = 0.050) in young (0.13 ± 0.01 F/D) compared with old (0.11 ± 0.003 F/D), but not between ND (0.12 ± 0.01 F/D) and sham (0.12 ± 0.01 F/D). Old animals who had received ND displayed elevated FSR in the gastrocnemius ( P = 0.054) and soleus ( P = 0.024).
Conclusions:
ND use in young adult animals appeared to maintain long-term elevations in FSR in muscle during aging.
Insights
Nandrolone decanoate (ND) increased kidney and muscle fractional synthetic rates (FSR) in mice. Long-term use of ND appeared to maintain elevated muscle FSR during aging.
Area of Science:
- Physiology
- Pharmacology
- Biochemistry
Background:
- Anabolic-androgenic steroids (AAS) like nandrolone decanoate (ND) are performance-enhancing drugs.
- Understanding the long-term effects of AAS on tissue synthesis is crucial for health and performance research.
Purpose of the Study:
- To investigate the acute and long-term impacts of nandrolone decanoate (ND) on fractional synthetic rates (FSR) in various tissues.
- To determine if ND administration influences tissue FSR during aging.
Main Methods:
- Male C57BL/6 mice were administered ND or a sham treatment for 6 weeks, starting at 7 months of age.
- Tissue samples (kidney, liver, heart, gastrocnemius, soleus) were analyzed for FSR using deuterated water labeling and liquid chromatography-tandem mass spectrometry.
- Animals were assessed at 1 week post-cessation and at 16 months of age to evaluate acute and long-term effects.
Main Results:
- Kidney FSR was elevated in ND-treated mice compared to sham and higher in younger compared to older mice.
- Liver and heart FSR were significantly higher in younger mice than in older mice, with no difference between ND and sham groups.
- Gastrocnemius FSR was higher in younger than older mice and also greater in ND-treated mice compared to sham.
- Soleus FSR was higher in younger mice, and old animals receiving ND showed elevated FSR in gastrocnemius and soleus muscles.
Conclusions:
- Nandrolone decanoate (ND) administration resulted in increased kidney and muscle fractional synthetic rates.
- Long-term ND use in young adult mice appeared to sustain elevated muscle FSR during the aging process.
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