Key result
Resistance training attenuated the decline in skeletal muscle function, including grip strength and maximal force, during incremental doxorubicin treatment in rats.
Why the study?
Resistance training prior to doxorubicin treatment attenuates skeletal muscle dysfunction, but the effect of resistance training during doxorubicin treatment is less known.
Does resistance training prevent skeletal muscle dysfunction during doxorubicin treatment in a rat model?
RCT (n=36)
randomly assigned
Does resistance training prevent skeletal muscle dysfunction during doxorubicin treatment in a rat model?
Low-intensity resistance training may attenuate the decline in skeletal muscle function during doxorubicin chemotherapy in a preclinical model.
RT during doxorubicin preserved muscle function in rats; hypothesis-generating for humans and requires clinical trials before any practice consideration.
Previous research has shown that resistance training (RT) before doxorubicin (DOX) treatment attenuates the decline in muscle dysfunction; however, the effect of RT during DOX treatment is less known. PURPOSE: Investigate the effects of RT before and during a 4-wk course of incremental DOX treatment on skeletal muscle function. METHODS: Male, Sprague-Dawley rats (N = 36) were randomly assigned to the following groups: sedentary+saline (SED + SAL), sedentary+DOX (SED + DOX), RT + SAL, or RT + DOX. The RT protocol utilized a raised cage model, which provided progressive hindlimb loading throughout the 14-wk study, whereas SED animals were kept in normal housing. Starting at week 10, DOX-treated animals received 3 mg·kg DOX weekly for 4 wk (12 mg·kg cumulative); whereas SAL-treated groups received 0.9% NaCl as a placebo. Grip strength was recorded at 0, 10, 12, and 14 wk. Ex vivo muscle function was performed on excised soleus (SOL) and extensor digitorum longus (EDL) from the right hind limb 5 d after the last injection and were analyzed for expression of creatine kinase (CK) and creatine transporters. RESULTS: SED + DOX-treated animals had significantly lower EDL mass compared with SED + SAL- and RT + DOX-treated animals. Grip strength, EDL maximal force, and EDL force development were significantly lower in SED + DOX-treated animals compared with RT + SAL and SED + SAL. No significant differences in EDL function were found between RT + DOX and RT + SAL animals. DOX treatment reduced expression of CK in the SOL, which abated with RT. CONCLUSIONS: Low-intensity RT may attenuate the decline in skeletal muscle function during incremental DOX treatment.
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Bredahl et al. (2020) conducted an RCT in doxorubicin-induced muscle dysfunction (n=36). Resistance training (RT) vs. Sedentary (SED) was evaluated on skeletal muscle function. Resistance training attenuated the decline in skeletal muscle function, including grip strength and maximal force, during incremental doxorubicin treatment in rats.
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