Caloric restriction reduces fiber loss and mitochondrial abnormalities in aged rat muscle

被引:125
作者
Aspnes, LE
Lee, CM
Weindruch, R
Chung, SS
Roecker, EB
Aiken, JM
机构
[1] UNIV WISCONSIN,DEPT NUTR SCI,MADISON,WI 53706
[2] UNIV WISCONSIN,DEPT MED,MADISON,WI 53706
[3] UNIV WISCONSIN,DEPT BIOSTAT,MADISON,WI 53706
[4] WILLIAM S MIDDLETON MEM VET ADM MED CTR,CTR GERIATR RES EDUC & CLIN,MADISON,WI 53706
关键词
aging; sarcopenia; mitochondria; skeletal muscle;
D O I
10.1096/fasebj.11.7.9212081
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
The influence of caloric restriction (CR) initiated at 17 months of age was investigated on selected age-associated measures in skeletal muscle. Tissue from young (3-4 months) ad libitum-fed, old (30-32 months) restricted (35% and 50% CR, designated CR35 and CR50, respectively), and old ad libitum-fed rats (29 months) was studied. CR preserved fiber number and fiber type composition in the vastus lateralis muscle of the CR50 rats. In the old rats from all groups, individual fibers were found with either no detectable cytochrome c oxidase activity (COX-), hyperreactivity for succinate dehydrogenase activity (SDH++; also known as ragged red fibers [RRF]), or both COX- and SDH++. Muscle from the CR50 rats contained significantly fewer COX- and SDH++ fibers than did the muscle from CR35 rats. CR50 rats also had significantly lower numbers of mtDNA deletion products in two (adductor longus and soleus) of the four muscles examined compared to CR35 rats. These data indicate that CR begun in late middle age can retard age-associated fiber loss and fiber type changes, as well as increases in the number of skeletal muscle fibers showing mitochondrial enzyme abnormalities. CR also decreased the accumulation of mtDNA deletions.
引用
收藏
页码:573 / 581
页数:9
相关论文
共 85 条
[51]  
MORAES CT, 1992, AM J HUM GENET, V50, P934
[52]   PROGRESSIVE LOSS OF CYTOCHROME-C-OXIDASE IN THE HUMAN EXTRAOCULAR-MUSCLES IN AGING - A CYTOCHEMICAL-IMMUNOHISTOCHEMICAL STUDY [J].
MULLERHOCKER, J ;
SCHNEIDERBANGER, K ;
STEFANI, FH ;
KADENBACH, B .
MUTATION RESEARCH, 1992, 275 (3-6) :115-124
[53]  
MULLERHOCKER J, 1990, J NEUROL SCI, V100, P14, DOI 10.1016/0022-510x(90)90006-9
[54]   DIFFERENT INSITU HYBRIDIZATION PATTERNS OF MITOCHONDRIAL-DNA IN CYTOCHROME-C OXIDASE-DEFICIENT EXTRAOCULAR-MUSCLE FIBERS IN THE ELDERLY [J].
MULLERHOCKER, J ;
SEIBEL, P ;
SCHNEIDERBANGER, K ;
KADENBACH, B .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1993, 422 (01) :7-15
[55]   Defects of the respiratory chain in various tissues of old monkeys: A cytochemical-immunocytochemical study [J].
MullerHocker, J ;
Schafer, S ;
Link, TA ;
Possekel, S ;
Hammer, C .
MECHANISMS OF AGEING AND DEVELOPMENT, 1996, 86 (03) :197-213
[56]   AGE-RELATED-CHANGES IN THE REDOX STATUS OF RAT MUSCLE-CELLS AND THEIR ROLE IN ENZYME-AGING [J].
NOY, N ;
SCHWARTZ, H ;
GAFNI, A .
MECHANISMS OF AGEING AND DEVELOPMENT, 1985, 29 (01) :63-69
[57]   Alterations of superoxide dismutase iso-enzyme activity, content, and mRNA expression with aging in rat skeletal muscle [J].
OhIshi, S ;
Kizaki, T ;
Yamashita, H ;
Nagata, N ;
Suzuki, K ;
Taniguchi, N ;
Ohno, H .
MECHANISMS OF AGEING AND DEVELOPMENT, 1995, 84 (01) :65-76
[58]  
PRELLE A, 1994, ACTA NEUROPATHOL, V87, P371
[59]   NORMAL OXIDATIVE DAMAGE TO MITOCHONDRIAL AND NUCLEAR-DNA IS EXTENSIVE [J].
RICHTER, C ;
PARK, JW ;
AMES, BN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (17) :6465-6467
[60]   RAGGED-RED FIBERS IN NORMAL AGING AND INFLAMMATORY MYOPATHY [J].
RIFAI, Z ;
WELLE, S ;
KAMP, C ;
THORNTON, CA .
ANNALS OF NEUROLOGY, 1995, 37 (01) :24-29