Reduced mitochondrial ROS, enhanced antioxidant defense, and distinct age-related changes in oxidative damage in muscles of long-lived Peromyscus leucopus

被引:33
作者
Shi, Yun [1 ,2 ]
Pulliam, Daniel A. [1 ,2 ]
Liu, Yuhong [1 ,2 ]
Hamilton, Ryan T. [1 ,2 ]
Jernigan, Amanda L. [1 ,2 ]
Bhattacharya, Arunabh [1 ,2 ]
Sloane, Lauren B. [1 ]
Qi, Wenbo [1 ,2 ]
Chaudhuri, Asish [1 ,3 ,5 ]
Buffenstein, Rochelle [1 ,4 ]
Ungvari, Zoltan [6 ]
Austad, Steven N. [1 ,2 ]
Van Remmen, Holly [1 ,2 ,4 ,5 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Sam & Ann Barshop Inst Longev & Aging Studies, San Antonio, TX 78245 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Cell & Struct Biol, San Antonio, TX 78245 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Biochem, San Antonio, TX 78245 USA
[4] Univ Texas Hlth Sci Ctr San Antonio, Dept Physiol, San Antonio, TX 78245 USA
[5] South Texas Vet Hlth Care Syst, San Antonio, TX USA
[6] Univ Oklahoma, Hlth Sci Ctr, Dept Geriatr Med, Reynolds Oklahoma Ctr Aging, Oklahoma City, OK USA
关键词
Peromyscus leucopus; mitochondria; reactive oxygen species; skeletal muscle; oxidative damage; comparative biology of aging; HYDROGEN-PEROXIDE PRODUCTION; SKELETAL-MUSCLE; UNCOUPLING PROTEIN-3; SUPEROXIDE-DISMUTASE; ELECTRON-TRANSPORT; STRESS RESISTANCE; MOUSE HINDLIMB; FIBER TYPES; LONGEVITY; MICE;
D O I
10.1152/ajpregu.00139.2012
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Shi Y, Pulliam DA, Liu Y, Hamilton RT, Jernigan AL, Bhattacharya A, Sloane LB, Qi W, Chaudhuri A, Buffenstein R, Ungvari Z, Austad SN, Van Remmen H. Reduced mitochondrial ROS, enhanced antioxidant defense, and distinct age-related changes in oxidative damage in muscles of long-lived Peromyscus leucopus. Am J Physiol Regul Integr Comp Physiol 304: R343-R355, 2013. First published January 16, 2013; doi:10.1152/ajpregu.00139.2012.-Comparing biological processes in closely related species with divergent life spans is a powerful approach to study mechanisms of aging. The oxidative stress hypothesis of aging predicts that longer-lived species would have lower reactive oxygen species (ROS) generation and/or an increased antioxidant capacity, resulting in reduced oxidative damage with age than in shorter-lived species. In this study, we measured ROS generation in the young adult animals of the long-lived white-footed mouse, Peromyscus leucopus (maximal life span potential, MLSP = 8 yr) and the common laboratory mouse, Mus musculus (C57BL/6J strain; MLSP = 3.5 yr). Consistent with the hypothesis, our results show that skeletal muscle mitochondria from adult P. leucopus produce less ROS (superoxide and hydrogen peroxide) compared with M. musculus. Additionally, P. leucopus has an increase in the activity of antioxidant enzymes superoxide dismutase 1, catalase, and glutathione peroxidase 1 at young age. P. leucopus compared with M. musculus display low levels of lipid peroxidation (isoprostanes) throughout life; however, P. leucopus although having elevated protein carbonyls at a young age, the accrual of protein oxidation with age is minimal in contrast to the linear increase in M. musculus. Altogether, the results from young animals are in agreement with the predictions of the oxidative stress hypothesis of aging with the exception of protein carbonyls. Nonetheless, the age-dependent increase in protein carbonyls is more pronounced in short-lived M. musculus, which supports enhanced protein homeostasis in long-lived P. leucopus.
引用
收藏
页码:R343 / R355
页数:13
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