Departamento de Anatomia, Biologia Celular, Fisiologia e Biofísica, Instituto de Biologia, Universidade Estadual de Campinas, Campinas, São Paulo, Brazil.
Nutrition. 2012 Jun;28(6):686-90. doi: 10.1016/j.nut.2011.09.013. Epub 2011 Dec 20.
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.
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-α (a proinflammatory cytokine) and 4-hydroxynonenal (a marker of lipid peroxidation) were analyzed by immunoblotting.
Ascorbic acid decreased creatine kinase levels, myonecrosis, inflammation, and the levels of tumor necrosis factor-α and 4-hydroxynonenal.
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.
氧化应激导致 mdx 小鼠和杜氏肌营养不良症中缺乏 dystrophin 的纤维发生肌坏死。我们研究了抗氧化剂和自由基清除剂抗坏血酸 (AA) 对营养不良性膈肌肌肉的影响。
14 天大的 mdx 小鼠接受 AA 治疗 14 天。对照 mdx 小鼠接受生理盐水。通过 Evans 蓝染料渗透到肌纤维来可视化肌肉损伤,并通过组织学分析评估炎症程度。通过免疫印迹分析肿瘤坏死因子-α(一种促炎细胞因子)和 4-羟壬烯醛(脂质过氧化的标志物)的水平。
抗坏血酸降低了肌酸激酶水平、肌坏死、炎症以及肿瘤坏死因子-α和 4-羟壬烯醛的水平。
目前的结果表明,AA 通过减少活性氧发挥对营养不良性肌肉变性的保护作用,并支持进一步研究 AA 作为治疗肌营养不良症的潜在疗法。