Effects of caloric restriction on skeletal muscle mitochondrial proton leak in aging rats

被引:69
作者
Lal, SB
Ramsey, JJ
Monemdjou, S
Weindruch, R
Harper, ME
机构
[1] Univ Ottawa, Fac Med, Dept Biochem Microbiol & Immunol, Ottawa, ON K1H 8M5, Canada
[2] Univ Wisconsin, Wisconsin Reg Primate Res Ctr, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Med, Madison, WI 53706 USA
[4] Vet Adm Geriatr Res Educ & Clin Ctr, Madison, WI USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2001年 / 56卷 / 03期
关键词
D O I
10.1093/gerona/56.3.B116
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
Long-term caloric restriction (CR) retards aging processes and increases maximum life span. We investigated the influence of CR on mitochondrial proton leaks in rat skeletal muscle. Because CR lowers oxidative damage to mitochondrial membrane lipids and proteins, we hypothesized that leak would be lower in mitochondria from old CR rats than in age-matched controls. Three groups (n = 12) were studied: 4-month-old "young" control rats (body weight: 404 g +/- 7 SEM), 33-month-old CR rats (body weight: 262 g +/- 3), and 33-month-old control rats (body weight: 446 g +/- 5). CR rats received 67% of the energy intake of old control rats, with adequate intakes of all essential nutrients. Maximum leak-dependent O-2 consumption (State 3) was 23% lower in CR rats than in age-matched controls, whereas protonmotive force values were similar, supporting our hypothesis. The overall kinetics of leak were similar between the two groups of old rats; in the young, kinetics indicated higher protonmotive force values. The latter indication is consistent with aging-induced alterations in proton leak kinetics that are independent of dietary intervention. There was no influence of age or diet on serum T-4 level, whereas T-3 was lower in young than in old control rats. These results support and extend the oxidative stress hypothesis of aging.
引用
收藏
页码:B116 / B122
页数:7
相关论文
共 41 条
  • [1] OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING
    AMES, BN
    SHIGENAGA, MK
    HAGEN, TM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) : 7915 - 7922
  • [2] ISOLATION OF SKELETAL-MUSCLE MITOCHONDRIA FROM HAMSTERS USING AN IONIC MEDIUM CONTAINING ETHYLENEDIARNINETETRAACETIC ACID AND NAGARSE
    BHATTACHARYA, SK
    THAKAR, JH
    JOHNSON, PL
    SHANKLIN, DR
    [J]. ANALYTICAL BIOCHEMISTRY, 1991, 192 (02) : 344 - 349
  • [3] The uncoupling proteins, a review
    Boss, O
    Muzzin, P
    Giacobino, JP
    [J]. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1998, 139 (01) : 1 - 9
  • [4] Uncoupling protein-3: A new member of the mitochondrial carrier family with tissue-specific expression
    Boss, O
    Samec, S
    PaoloniGiacobino, A
    Rossier, C
    Dulloo, A
    Seydoux, J
    Muzzin, P
    Giacobino, JP
    [J]. FEBS LETTERS, 1997, 408 (01) : 39 - 42
  • [5] EVOLUTION OF ENERGY-METABOLISM - PROTON PERMEABILITY OF THE INNER MEMBRANE OF LIVER-MITOCHONDRIA IS GREATER IN A MAMMAL THAN IN A REPTILE
    BRAND, MD
    COUTURE, P
    ELSE, PL
    WITHERS, KW
    HULBERT, AJ
    [J]. BIOCHEMICAL JOURNAL, 1991, 275 : 81 - 86
  • [6] Brookes PS, 1998, J NEUROCHEM, V70, P2195
  • [7] THERMODYNAMIC CONTROL OF ELECTRON FLUX THROUGH MITOCHONDRIAL CYTOCHROME BC1 COMPLEX
    BROWN, GC
    BRAND, MD
    [J]. BIOCHEMICAL JOURNAL, 1985, 225 (02) : 399 - 405
  • [8] CHEN RF, 1967, J BIOL CHEM, V242, P173
  • [9] Davies KJA, 1995, BIOCHEM SOC SYMP, P1, DOI 10.1042/bss0610001
  • [10] Uncoupling protein-2: A novel gene linked to obesity and hyperinsulinemia
    Fleury, C
    Neverova, M
    Collins, S
    Raimbault, S
    Champigny, O
    LeviMeyrueis, C
    Bouillaud, F
    Seldin, MF
    Surwit, RS
    Ricquier, D
    Warden, CH
    [J]. NATURE GENETICS, 1997, 15 (03) : 269 - 272