Mitochondrial oxidative stress and the metabolic syndrome

被引:121
|
作者
James, Andrew M. [1 ]
Collins, Yvonne [1 ]
Logan, Angela [1 ]
Murphy, Michael P. [1 ]
机构
[1] MRC, Mitochondrial Biol Unit, Cambridge CB2 0XY, England
来源
TRENDS IN ENDOCRINOLOGY AND METABOLISM | 2012年 / 23卷 / 09期
基金
英国生物技术与生命科学研究理事会;
关键词
INSULIN-RESISTANCE; SUPEROXIDE-DISMUTASE; ANTIOXIDANT DEFENSE; SIGNAL-TRANSDUCTION; SKELETAL-MUSCLE; MECHANISMS; CELLS; H2O2; ACONITASE; PROTEINS;
D O I
10.1016/j.tem.2012.06.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The current epidemic of the metabolic syndrome in the developed world is largely due to overnutrition and lack of physical activity. However, the underlying causes by which chronic overnutrition interacts with genotype and physical inactivity to generate the metabolic syndrome phenotype are complex, and include multiple metabolic and physiological alterations. Mitochondrial oxidative stress has been suggested to contribute to the metabolic syndrome, but the mechanisms and significance are unclear. Here we review how disruption of mitochondrial metabolism and increased oxidative stress may occur during overnutrition coupled with limited physical activity. From this we suggest a unifying hypothesis to integrate what is known about mitochondrial involvement in the metabolic syndrome that points to testable hypotheses and novel therapeutic approaches.
引用
收藏
页码:429 / 434
页数:6
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