Caloric restriction protects mitochondrial function with aging in skeletal and cardiac muscles

被引:76
作者
Hepple, RT
Baker, DJ
McConkey, M
Murynka, T
Norris, R
机构
[1] Univ Calgary, Fac Kinesiol, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Fac Med, Calgary, AB T2N 1N4, Canada
关键词
D O I
10.1089/rej.2006.9.219
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
In skeletal muscles and heart in vitro complex IV activity is lower in young adult caloric restricted (CR) animals despite normal aerobic function in situ and in vivo. On the other hand, whereas markers of oxidative capacity decline 25% to 46% between 8 and 10 months and 35 months in ad libitum fed (AL) animals, in most muscles there is no decline in CR across the same absolute age (35 mo old) or relative age (35% survival rate) span and PGC-1 alpha gene expression in gastrocnemius muscle declines more slowly with aging. The present results show that CR largely prevents the age-associated decline in mitochondrial function in heart and skeletal muscles, and suggest that this is secondary to a better-maintained drive on mitochondrial biogenesis.
引用
收藏
页码:219 / 222
页数:4
相关论文
共 20 条
[1]  
BEVILACQUA L, 2004, AM J PHYSIOL-ENDOC M, V286, pE582
[2]   Modulation of Lon protease activity and aconitase turnover during aging and oxidative stress [J].
Bota, DA ;
Van Remmen, H ;
Davies, KJA .
FEBS LETTERS, 2002, 532 (1-2) :103-106
[3]  
COGGAN AR, 1992, J GERONTOL, V47, P71
[4]   Oxidative capacity and ageing in human muscle [J].
Conley, KE ;
Jubrias, SA ;
Esselman, PC .
JOURNAL OF PHYSIOLOGY-LONDON, 2000, 526 (01) :203-210
[5]   Influences of age and dietary restriction on gastrocnemius electron transport system activities in mice [J].
Desai, VG ;
Weindruch, R ;
Hart, RW ;
Feuers, RJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1996, 333 (01) :145-151
[6]   HISTOCHEMICAL AND METABOLIC CHARACTERISTICS OF HUMAN SKELETAL-MUSCLE IN RELATION TO AGE [J].
ESSENGUSTAVSSON, B ;
BORGES, O .
ACTA PHYSIOLOGICA SCANDINAVICA, 1986, 126 (01) :107-114
[7]   Aging selectively decreases oxidative capacity in rat heart interfibrillar mitochondria [J].
Fannin, SW ;
Lesnefsky, EJ ;
Slabe, TJ ;
Hassan, MO ;
Hoppel, CL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1999, 372 (02) :399-407
[8]   Caloric restriction decreases mitochondrial free radical generation at complex I and lowers oxidative damage to mitochondrial DNA in the rat heart [J].
Gredilla, R ;
Sanz, A ;
Lopez-Torres, M ;
Barja, G .
FASEB JOURNAL, 2001, 15 (07) :1589-+
[9]   Skeletal muscle aging in F344BNF1-hybrid rats:: I.: Mitochondrial dysfunction contributes to the age-associated reduction in VO2max [J].
Hagen, JL ;
Krause, DJ ;
Baker, DJ ;
Fu, MH ;
Tarnopolsky, MA ;
Hepple, RT .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2004, 59 (11) :1099-1110
[10]   Long-term caloric restriction abrogates the age-related decline in skeletal muscle aerobic function [J].
Hepple, RT ;
Baker, DJ ;
Kaczor, JJ ;
Krause, DJ .
FASEB JOURNAL, 2005, 19 (08) :1320-+