4.4 Article

PROGRESSIVE RESISTANCE VOLUNTARY WHEEL RUNNING IN THE mdx MOUSE

期刊

MUSCLE & NERVE
卷 42, 期 6, 页码 871-880

出版社

WILEY
DOI: 10.1002/mus.21764

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cytoskeletal proteins; Duchenne muscular dystrophy; exercise; physical activity; skeletal muscle function

资金

  1. Muscular Dystrophy Association [MDA4143]

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Exercise training has been minimally explored as a therapy to mitigate the loss of muscle strength for individuals with Duchenne muscular dystrophy (DMD). Voluntary wheel running is known to elicit beneficial adaptations in the mdx mouse model for DMD. The aim of this study was to examine progressive resistance wheel running in mdx mice by comprehensively testing muscle function before, during, and after a 12-week training period. Male mdx mice at similar to 4 weeks age were randomized into three groups: Sedentary, Free Wheel, and Resist Wheel. Muscle strength was assessed via in vivo dorsiflexion torque, grip strength, and whole body tension intermittently throughout the training period. Contractility of isolated soleus muscles was analyzed at the study's conclusion. Both Free and Resist Wheel mice had greater grip strength (similar to 22%) and soleus muscle specific tetanic force (26%) compared with Sedentary mice. This study demonstrates that two modalities of voluntary exercise are beneficial to dystrophic muscle and may help establish parameters for an exercise prescription for DMD. Muscle Nerve 42: 871-880, 2010

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