Ascorbic acid protects the diaphragm muscle against myonecrosis in mdx mice

被引:29
|
作者
Tonon, Erika [1 ]
Ferretti, Renato [1 ]
Shiratori, Jean Hideki [1 ]
Santo Neto, Humberto [1 ]
Marques, Maria Julia [1 ]
Minatel, Elaine [1 ]
机构
[1] Univ Estadual Campinas, Dept Anat Biol Celular Fisiol & Biofis, Inst Biol, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Mdx mice; Diaphragm muscle; Ascorbic acid; Oxidative stress; Tumor necrosis factor-alpha; KAPPA-B ACTIVATION; TUMOR-NECROSIS-FACTOR; GREEN TEA EXTRACT; SKELETAL-MUSCLE; VITAMIN-C; OXIDATIVE STRESS; NEUROMUSCULAR-JUNCTION; DYSTROPHIC MUSCLE; EVANS BLUE; IN-VIVO;
D O I
10.1016/j.nut.2011.09.013
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Objective: Oxidative stress contributes to myonecrosis in the dystrophin-deficient fibers of mdx mice and in Duchenne's muscular dystrophy. We examined the effects of ascorbic acid (AA), an antioxidant and free radical scavenger, on the dystrophic diaphragm muscle. Methods: Mdx mice (14 d old) received AA for 14 d. Control mdx mice received saline. The muscle damage was visualized by the penetration of Evans blue dye into myofibers and the extent of inflammation was assessed by histologic analysis. Creatine kinase levels were measured for the biochemical evaluation of muscle fiber degeneration. The levels of tumor necrosis factor-alpha (a proinflammatory cytokine) and 4-hydroxynonenal (a marker of lipid peroxidation) were analyzed by immunoblotting. Results: Ascorbic acid decreased creatine kinase levels, myonecrosis, inflammation, and the levels of tumor necrosis factor-alpha and 4-hydroxynonenal. Conclusion: The present results suggest that AA plays a protective role in dystrophic muscle degeneration, possibly by decreasing reactive oxygen species, and support further investigations of AA as a potential therapy for dystrophinopathies. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:686 / 690
页数:5
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