期刊
NEUROMUSCULAR DISORDERS
卷 12, 期 2, 页码 174-182出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0960-8966(01)00273-5
关键词
calcium; creatine; creatine kinase; Duchenne muscular dystrophy; mdx mouse; mitochondria; muscle; muscular disease; permeability transition; respiration
The mdx mouse serves as animal model for Duchenne muscular dystrophy. Energy status in muscles of mdx mice is impaired and we have demonstrated recently that the energy precursor creatine exerts beneficial effects on mdx skeletal muscle cells in culture. Here we show that feeding a creatine-enriched diet to new-born mdx mice strongly reduced the first wave of muscle necrosis four weeks after birth. Necrosis of the fast-twitch muscle extensor digitorum longus was inhibited by 63 +/- 14% (P<0.0001) while necrosis of the slow-switch soleus muscle was not significantly decreased. In addition, using chemically skinned muscle fibres,, we found that mitochondrial respiration capacity was decreased by about 25% in mdx-derived fibres and that long-term creatine-feeding restored respiration to wild, type levels. These results provide evidence that creatine supplementation in mdx mice improves muscle health and may provide a scientific basis for its use as adjuvant therapy in Duchenne muscular dystrophy. (C) 2002 Elsevier Science B.V. All rights reserved.
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