Colin J Quinn1,2, David S Hydock2,3. 1. Aerospace and Operational Physiology, United State Air Force, Tyndall AFB, USA. 2. School of Sport and Exercise Science, University of Northern Colorado, USA. 3. Cancer Rehabilitation Institute, University of Northern Colorado, USA.
Abstract
BACKGROUND: The skeletal muscle toxicity that accompanies the chemotherapy drug doxorubicin (DOX) may lead to cancer patient weakness and fatigue. This myotoxicity involves myogenic regulatory factor (MRF) disruption which alters muscle integrity and regeneration. Endurance exercise enhances MRF expression and thereby may mitigate DOX-induced MRF disruptions. This study examined the effects of endurance training and DOX treatment on myogenic regulatory factor (MRF) expression. METHODS: Male rats were exercise trained (EXER) or remained sedentary (SED) for two weeks. EXER and SED then received either DOX (15 mg/kg) or saline (SAL). Soleus, extensor digitorum longus (EDL), and diaphragm were excised 24 hours post injection, and MRF expression was analyzed. RESULTS: Significant Myf5 drug and activity effects were observed in the soleus with EXER+DOX expressing higher Myf5 than SED+DOX. A significant drug effect was detected in soleus MyoD, and a significant activity effect was detected in soleus Mrf4. No main effects or interactions were observed in the EDL, but in the diaphragm, a significant activity effect was observed for Myf5 with EXER+DOX expressing higher levels than SED+DOX. CONCLUSION: Doxorubicin treatment increased soleus MRFs and exercise boosted MRF response in soleus and diaphragm suggesting that exercise may enhance regenerative signaling with DOX treatment. LEVEL OF EVIDENCE: I b, individual randomized controlled trial.
BACKGROUND: The skeletal muscle toxicity that accompanies the chemotherapy drug doxorubicin (DOX) may lead to cancer patient weakness and fatigue. This myotoxicity involves myogenic regulatory factor (MRF) disruption which alters muscle integrity and regeneration. Endurance exercise enhances MRF expression and thereby may mitigate DOX-induced MRF disruptions. This study examined the effects of endurance training and DOX treatment on myogenic regulatory factor (MRF) expression. METHODS: Male rats were exercise trained (EXER) or remained sedentary (SED) for two weeks. EXER and SED then received either DOX (15 mg/kg) or saline (SAL). Soleus, extensor digitorum longus (EDL), and diaphragm were excised 24 hours post injection, and MRF expression was analyzed. RESULTS: Significant Myf5 drug and activity effects were observed in the soleus with EXER+DOX expressing higher Myf5 than SED+DOX. A significant drug effect was detected in soleus MyoD, and a significant activity effect was detected in soleus Mrf4. No main effects or interactions were observed in the EDL, but in the diaphragm, a significant activity effect was observed for Myf5 with EXER+DOX expressing higher levels than SED+DOX. CONCLUSION: Doxorubicin treatment increased soleus MRFs and exercise boosted MRF response in soleus and diaphragm suggesting that exercise may enhance regenerative signaling with DOX treatment. LEVEL OF EVIDENCE: I b, individual randomized controlled trial.
Entities:
Keywords:
anthracycline; diaphragm; fast muscle; slow muscle
Authors: S M DeAtley; M Y Aksenov; M V Aksenova; B Harris; R Hadley; P Cole Harper; J M Carney; D A Butterfield Journal: Cancer Lett Date: 1999-02-08 Impact factor: 8.679
Authors: Eric C Bredahl; Keith B Pfannenstiel; Colin J Quinn; Reid Hayward; David S Hydock Journal: Med Sci Sports Exerc Date: 2016-08 Impact factor: 5.411