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Updated: Mar 11, 2026

Induction and Assessment of Exertional Skeletal Muscle Damage in Humans
Published on: December 11, 2016
Doxorubicin inhibits muscle inflammation after eccentric exercise
Sheng-Chih Huang1, Jin-Fu Wu1, Suchada Saovieng1
1Laboratory of Exercise Biochemistry, University of Taipei, Taipei, Taiwan.
Doxorubicin treatment impairs skeletal muscle inflammation by depleting M1 macrophages during exercise. Long-term doxorubicin use causes significant muscle loss and accelerated death, which coenzyme Q10 cannot reverse.
Area of Science:
- Oncology
- Exercise Physiology
- Immunology
Background:
- Doxorubicin is a vital anti-cancer drug but causes muscle wasting in patients.
- Understanding doxorubicin's impact on skeletal muscle is crucial for patient care.
Purpose of the Study:
- To investigate doxorubicin's effects on macrophage distribution in exercised skeletal muscle.
- To evaluate the impact of long-term doxorubicin treatment on muscle mass and survival.
- To assess the potential of coenzyme Q10 supplementation to mitigate doxorubicin-induced effects.
Main Methods:
- Rats received acute or long-term doxorubicin injections.
- Soleus muscles were analyzed for macrophage infiltration (M1 and M2) after eccentric exercise.
- Muscle mass, survival rates, and inflammatory markers were assessed.
- Coenzyme Q10 supplementation was administered in some groups.
Main Results:
- Doxorubicin treatment altered inflammatory markers (TNF-alpha, IL-10) in non-exercised muscle.
- Exercise-induced M1 macrophage infiltration and inflammation were reduced in doxorubicin-treated rats.
- Long-term doxorubicin administration led to significant muscle loss and reduced survival.
- Coenzyme Q10 did not reverse muscle loss or improve survival in long-term treatment.
Conclusions:
- Doxorubicin impairs the inflammatory response in exercised skeletal muscle by depleting M1 macrophages.
- Prolonged doxorubicin treatment results in irreversible muscle loss and decreased survival, unaffected by coenzyme Q10.
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