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铜锌超氧化物歧化酶的缺失会导致氧化应激增加以及与年龄相关的骨骼肌萎缩加速。

Absence of CuZn superoxide dismutase leads to elevated oxidative stress and acceleration of age-dependent skeletal muscle atrophy.

作者信息

Muller Florian L, Song Wook, Liu Yuhong, Chaudhuri Asish, Pieke-Dahl Sandra, Strong Randy, Huang Ting-Ting, Epstein Charles J, Roberts L Jackson, Csete Marie, Faulkner John A, Van Remmen Holly

机构信息

Department of Cellular and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229-3900, USA.

出版信息

Free Radic Biol Med. 2006 Jun 1;40(11):1993-2004. doi: 10.1016/j.freeradbiomed.2006.01.036. Epub 2006 Feb 17.

Abstract

We describe a novel phenotype in mice lacking the major antioxidant enzyme, CuZn-superoxide dismutase (Sod1(-/-) mice), namely a dramatic acceleration of age-related loss of skeletal muscle mass. Sod1(-/-) mice are 17 to 20% smaller and have a significantly lower muscle mass than wild-type mice as early as 3 to 4 months of age. Muscle mass in the Sod1(-/-) mice is further reduced with age and by 20 months, the hind-limb muscle mass in Sod1(-/-) mice is nearly 50% lower than in age-matched wild-type mice. Skeletal muscle tissue from young Sod1(-/-) mice has elevated oxidative damage to proteins, lipids, and DNA compared to muscle from young wild-type mice. The reduction in muscle mass and elevated oxidative damage are accompanied by a 40% decrease in voluntary wheel running by 6 months of age and decreased performance on the Rota-rod test at 13 months of age, but are not associated with a decline in overall spontaneous activity. In some of the old Sod1(-/-) mice, the loss in muscle mass is also associated with the presence of tremors and gait disturbances. Thus, the absence of CuZnSOD imposes elevated oxidative stress, loss of muscle mass, and physiological consequences that resemble an acceleration of normal age-related sarcopenia.

摘要

我们描述了一种在缺乏主要抗氧化酶铜锌超氧化物歧化酶的小鼠(Sod1(-/-)小鼠)中出现的新表型,即与年龄相关的骨骼肌质量损失显著加速。早在3至4个月大时,Sod1(-/-)小鼠就比野生型小鼠小17%至20%,且肌肉质量明显更低。随着年龄增长,Sod1(-/-)小鼠的肌肉质量进一步下降,到20个月时,Sod1(-/-)小鼠的后肢肌肉质量比年龄匹配的野生型小鼠低近50%。与年轻野生型小鼠的肌肉相比,年轻Sod1(-/-)小鼠的骨骼肌组织对蛋白质、脂质和DNA的氧化损伤增加。肌肉质量的减少和氧化损伤的增加伴随着6个月大时自愿轮转运动减少40%以及13个月大时在转棒试验中的表现下降,但与总体自发活动的下降无关。在一些老年Sod1(-/-)小鼠中,肌肉质量的损失还与震颤和步态障碍的出现有关。因此,缺乏铜锌超氧化物歧化酶会导致氧化应激增加、肌肉质量损失以及类似于正常年龄相关肌肉减少症加速的生理后果。

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