Effect of caloric restriction on mitochondrial reactive oxygen species production and bioenergetics: reversal by insulin

被引:100
作者
Lambert, AJ [1 ]
Merry, BJ [1 ]
机构
[1] Univ Liverpool, Sch Biol Sci, Liverpool L69 7ZB, Merseyside, England
关键词
control analysis; aging;
D O I
10.1152/ajpregu.00341.2003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
To gain insight into the antiaging mechanisms of caloric restriction (CR), mitochondria from liver tissue of male Brown Norway rats were used to study the effects of CR and insulin on mitochondrial reactive oxygen species production and bioenergetics. As assessed by hydrogen peroxide measurement, CR resulted in a decrease in the production rate of reactive oxygen species. This decrease was attributed to a decrease in protonmotive force in mitochondria from the CR animals. The decrease in protonmotive force resulted from an increase in proton leak activity and a concomitant decrease in substrate oxidation activity. Each of these effects of CR was reversed by subjecting CR animals to 2 wk of insulin treatment. To achieve continuous and stable insulin delivery, animals were placed under temporary halothane anesthesia and miniosmotic pumps were implanted subcutaneously. To gain further insight into how CR and insulin exerted its effects on mitochondrial bioenergetics, the effects of CR and insulin were quantified using modular metabolic control analysis. This analysis revealed that the effects of CR were transmitted through different reaction branches of the bioenergetic system, and insulin reversed the effects of CR by acting through the same branches. These results provide a plausible mechanism by which mitochondrial reactive oxygen species production is lowered by CR and a complete description of the effects of CR on mitochondrial bioenergetics. They also indicate that these changes may be due to lowered insulin concentrations and altered insulin signaling in the CR animal.
引用
收藏
页码:R71 / R79
页数:9
相关论文
共 48 条
[1]   Internal regulation of ATP turnover, glycolysis and oxidative phosphorylation in rat hepatocytes [J].
Ainscow, EK ;
Brand, MD .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 266 (03) :737-749
[2]   The responses of rat hepatocytes to glucagon and adrenaline - Application of quantified elasticity analysis [J].
Ainscow, EK ;
Brand, MD .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 265 (03) :1043-1055
[3]   Top-down control analysis of ATP turnover, glycolysis and oxidative phosphorylation in rat hepatocytes [J].
Ainscow, EK ;
Brand, MD .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 263 (03) :671-685
[4]   Longevity - Extending the lifespan of long-lived mice [J].
Bartke, A ;
Wright, JC ;
Mattison, JA ;
Ingram, DK ;
Miller, RA ;
Roth, GS .
NATURE, 2001, 414 (6862) :412-412
[5]   Extended longevity in mice lacking the insulin receptor in adipose tissue [J].
Blüher, M ;
Kahn, BB ;
Kahn, CR .
SCIENCE, 2003, 299 (5606) :572-574
[6]   Top down metabolic control analysis [J].
Brand, MD .
JOURNAL OF THEORETICAL BIOLOGY, 1996, 182 (03) :351-360
[7]  
BRAND MD, 1995, BIOENERGETICS PRACTI, P39
[8]   Caloric restriction promotes genomic stability by induction of base excision, repair and reversal of its age-related decline [J].
Cabelof, DC ;
Yanamadala, S ;
Raffoul, JJ ;
Guo, ZM ;
Soofi, A ;
Heydari, AR .
DNA REPAIR, 2003, 2 (03) :295-307
[9]   Mitochondrial free radical generation, oxidative stress, and aging [J].
Cadenas, E ;
Davies, KJA .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (3-4) :222-230
[10]   Extension of life-span by loss of CHICO, a Drosophila insulin receptor substrate protein [J].
Clancy, DJ ;
Gems, D ;
Harshman, LG ;
Oldham, S ;
Stocker, H ;
Hafen, E ;
Leevers, SJ ;
Partridge, L .
SCIENCE, 2001, 292 (5514) :104-106