The Mitochondrial Free Radical Theory of Aging

被引:145
作者
Barja, Gustavo [1 ]
机构
[1] Univ Complutense, Fac Biol Sci, Dept Anim Physiol 2, E-28040 Madrid, Spain
来源
MITOCHONDRION IN AGING AND DISEASE | 2014年 / 127卷
关键词
OXIDATIVE DNA-DAMAGE; MAXIMUM LIFE-SPAN; METHIONINE SULFOXIDE REDUCTASE; HYDROGEN-PEROXIDE PRODUCTION; FATTY-ACID UNSATURATION; COMPLEX-I CONTENT; CALORIC RESTRICTION; DIETARY RESTRICTION; RAT-LIVER; PROTEIN RESTRICTION;
D O I
10.1016/B978-0-12-394625-6.00001-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The mitochondrial free radical theory of aging is reviewed. Only two parameters currently correlate with species longevity in the right sense: the mitochondrial rate of reactive oxygen species (mitROS) production and the degree of fatty acid unsaturation of tissue membranes. Both are low in long-lived animals. In addition, the best-known manipulation that extends longevity, dietary restriction, also decreases the rate of mitROS production and oxidative damage to mtDNA. The same occurs during protein restriction as well as during methionine restriction. These two manipulations also increase maximum longevity in rodents. The decrease in mitROS generation and oxidative stress that takes place in caloric restriction seems to be due to restriction of a single dietary substance: methionine. The information available supports a mitochondrial free radical theory of aging focused on low generation of endogenous damage and low sensitivity of membranes to oxidation in long-lived animals.
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收藏
页码:1 / 27
页数:27
相关论文
共 100 条
[1]
Dietary protein restriction decreases oxidative protein damage, peroxidizability index, and mitochondrial complex I content in rat liver [J].
Ayala, Victoria ;
Naudi, Alba ;
Sanz, Alberto ;
Caro, Pilar ;
Portero-Otin, Manuel ;
Barja, Gustavo ;
Pamplona, Reinald .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2007, 62 (04) :352-360
[2]
Localization at complex I and mechanism of the higher free radical production of brain nonsynaptic mitochondria in the short-lived rat than in the longevous pigeon [J].
Barja, G ;
Herrero, A .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1998, 30 (03) :235-243
[3]
Oxidative damage to mitochondrial DNA is inversely related to maximum life span in the heart and brain of mammals [J].
Barja, G ;
Herrero, A .
FASEB JOURNAL, 2000, 14 (02) :312-318
[4]
A DECREASE OF FREE-RADICAL PRODUCTION NEAR-CRITICAL TARGETS AS A CAUSE OF MAXIMUM LONGEVITY IN ANIMALS [J].
BARJA, G ;
CADENAS, S ;
ROJAS, C ;
LOPEZTORRES, M ;
PEREZCAMPO, R .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1994, 108 (04) :501-512
[5]
Aging in vertebrates, and the effect of caloric restriction: a mitochondrial free radical production-DNA damage mechanism? [J].
Barja, G .
BIOLOGICAL REVIEWS, 2004, 79 (02) :235-251
[6]
LOW MITOCHONDRIAL FREE-RADICAL PRODUCTION PER UNIT O-2 CONSUMPTION CAN EXPLAIN THE SIMULTANEOUS PRESENCE OF HIGH LONGEVITY AND HIGH AEROBIC METABOLIC-RATE IN BIRDS [J].
BARJA, G ;
CADENAS, S ;
ROJAS, C ;
PEREZCAMPO, R ;
LOPEZTORRES, M .
FREE RADICAL RESEARCH, 1994, 21 (05) :317-327
[7]
Barja G., 2011, LONGEVITY EVOLUTION
[8]
ROLE OF UBIQUINONE IN MITOCHONDRIAL GENERATION OF HYDROGEN-PEROXIDE [J].
BOVERIS, A ;
CADENAS, E ;
STOPPANI, AOM .
BIOCHEMICAL JOURNAL, 1976, 156 (02) :435-444
[9]
Brosnan JT, 2006, J NUTR, V136, p1636S, DOI 10.1093/jn/136.6.1636S
[10]
HEPATIC METABOLITES AND COFACTORS IN RIBOFLAVIN DEFICIENCY AND CALORIE RESTRICTION [J].
BURCH, HB ;
LOWRY, OH ;
BRADLEY, ME ;
MAX, PF .
AMERICAN JOURNAL OF PHYSIOLOGY, 1970, 219 (02) :409-&