Caloric restriction improves thermotolerance and reduces hyperthermia-induced cellular damage in old rats

被引:80
作者
Hall, DM
Oberley, TD
Moseley, PM
Buettner, GR
Oberley, LW
Weindruch, R
Kregel, KC
机构
[1] Univ Iowa, Integrat Physiol Lab, Dept Exercise Sci, Iowa City, IA 52242 USA
[2] Univ Iowa, Free Rad Res Inst, Iowa City, IA 52242 USA
[3] Univ Iowa, Radiat Res Lab, Iowa City, IA 52242 USA
[4] Univ New Mexico, Dept Internal Med, Albuquerque, NM 87131 USA
[5] VA Hosp, Pathol & Lab Med Serv, Madison, WI 53705 USA
[6] Univ Wisconsin, Sch Med, Dept Pathol, Madison, WI 53705 USA
[7] Univ Wisconsin, Dept Med, Madison, WI 53705 USA
[8] Vet Adm Geriat Res, Educ & Clin Ctr, Madison, WI 53705 USA
关键词
free radicals; oxidative stress; stress proteins; HSP70; aging; antioxidant enzymes;
D O I
10.1096/fasebj.14.1.78
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adult-onset, long-term caloric restriction (CR) prolongs maximum life span in laboratory rodents. However, the effect of this intervention on an organism's ability to cope with a physical challenge has not been explored. We investigates the influence of CR and aging on stress tolerance in old rats exposed to an environmental heating protocol on two consecutive days. We hypothesized that CR would increase heat tolerance by reducing cellular stress and subsequent accrual of oxidative injury. All calorically restricted rats survived both heat exposures compared with only 50% of their control-fed counterparts. CR also decreased heat-induced radical generation, stress protein accumulation, and cellular injury in the liver. In addition, heat stress stimulated marked induction of the antioxidant enzymes manganese-containing superoxide dismutase and catalase, along with strong nuclear catalase expression in liver samples from samples from rats subjected to CR. In contrast, stress-related induction of antioxidant enzymes was blunted, and nuclear catalase expression was unchanged from euthermic conditions in the control-fed group. These data suggest that CR reduces cellular injury and improves heat tolerance of old animals by lowering radical production and preserving cellular ability to adapt to stress through antioxidant enzyme induction and translocation of these proteins to the nucleus.
引用
收藏
页码:78 / 86
页数:9
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