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Updated: Jun 7, 2026

Tibial Nerve Transection - A Standardized Model for Denervation-induced Skeletal Muscle Atrophy in Mice
Published on: November 3, 2013
Differential alterations in gene expression profiles contribute to time-dependent effects of nandrolone to prevent
Weiping Qin1, Jiangping Pan, William A Bauman
1Center of Excellence for the Medical Consequences of Spinal Cord Injury, James J, Peters VA Medical Center, 130 West Kingsbridge Road, Bronx, New York 10468, USA.
Background:
Anabolic steroids, such as nandrolone, slow muscle atrophy, but the mechanisms responsible for this effect are largely unknown. Their effects on muscle size and gene expression depend upon time, and the cause of muscle atrophy. Administration of nandrolone for 7 days beginning either concomitantly with sciatic nerve transection (7 days) or 29 days later (35 days) attenuated denervation atrophy at 35 but not 7 days. We reasoned that this model could be used to identify genes that are regulated by nandrolone and slow denervation atrophy, as well as genes that might explain the time-dependence of nandrolone effects on such atrophy. Affymetrix microarrays were used to profile gene expression changes due to nandrolone at 7 and 35 days and to identify major gene expression changes in denervated muscle between 7 and 35 days.
Results:
Nandrolone selectively altered expression of 124 genes at 7 days and 122 genes at 35 days, with only 20 genes being regulated at both time points. Marked differences in biological function of genes regulated by nandrolone at 7 and 35 days were observed. At 35, but not 7 days, nandrolone reduced mRNA and protein levels for FOXO1, the mTOR inhibitor REDD2, and the calcineurin inhibitor RCAN2 and increased those for ApoD. At 35 days, correlations between mRNA levels and the size of denervated muscle were negative for RCAN2, and positive for ApoD. Nandrolone also regulated genes for Wnt signaling molecules. Comparison of gene expression at 7 and 35 days after denervation revealed marked alterations in the expression of 9 transcriptional coregulators, including Ankrd1 and 2, and many transcription factors and kinases.
Conclusions:
Genes regulated in denervated muscle after 7 days administration of nandrolone are almost entirely different at 7 versus 35 days. Alterations in levels of FOXO1, and of genes involved in signaling through calcineurin, mTOR and Wnt may be linked to the favorable action of nandrolone on denervated muscle. Marked changes in the expression of genes regulating transcription and intracellular signaling may contribute to the time-dependent effects of nandrolone on gene expression.
Insights
Nandrolone protects against muscle atrophy, but its effects on gene expression change over time. This study identified specific genes regulated by nandrolone at different time points, revealing mechanisms behind its muscle-preserving actions.
Area of Science:
- Muscle atrophy research
- Molecular biology
- Pharmacology
Background:
- Anabolic steroids like nandrolone can slow muscle atrophy, but the underlying mechanisms and time-dependent effects remain unclear.
- Understanding these mechanisms is crucial for developing effective therapeutic strategies for muscle wasting conditions.
Purpose of the Study:
- To investigate the time-dependent effects of nandrolone on gene expression in denervated muscle.
- To identify specific genes regulated by nandrolone that contribute to its muscle-protective effects.
- To elucidate the molecular pathways involved in nandrolone's action on muscle atrophy.
Main Methods:
- Utilized Affymetrix microarrays to profile gene expression in denervated muscle treated with nandrolone at 7 and 35 days.
- Compared gene expression profiles between different time points to identify nandrolone-regulated genes and changes in denervated muscle.
- Analyzed the correlation between mRNA levels and muscle size.
Main Results:
- Nandrolone differentially regulated 124 genes at 7 days and 122 genes at 35 days, with only 20 common genes.
- At 35 days, nandrolone reduced FOXO1, REDD2, and RCAN2, while increasing ApoD, correlating with muscle size.
- Nandrolone also modulated Wnt signaling pathway genes and altered expression of transcriptional coregulators, transcription factors, and kinases.
Conclusions:
- Gene expression changes induced by nandrolone in denervated muscle are distinct at 7 and 35 days.
- Regulated genes, including FOXO1 and those in calcineurin, mTOR, and Wnt signaling pathways, may mediate nandrolone's beneficial effects on muscle.
- Time-dependent alterations in transcription and intracellular signaling genes likely contribute to nandrolone's complex effects on muscle atrophy.
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