Oxidative damage and age-related functional declines

被引:131
作者
Martin, I
Grotewiel, MS
机构
[1] Virginia Commonwealth Univ, Sch Med, Dept Human Genet, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Sch Med, Program Neurosci, Richmond, VA 23298 USA
关键词
aging; senescence; oxidative damage; antioxidants;
D O I
10.1016/j.mad.2006.01.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Most organisms experience progressive declines in physiological function as they age. Since this senescence of function is thought to underlie the decrease in quality of life in addition to the increase in susceptibility to disease and death associated with aging, identifying the mechanisms involved would be highly beneficial. One of the leading mechanistic theories for aging is the oxidative damage hypothesis. A number of studies in a variety of species support a strong link between oxidative damage and life span determination. The role of oxidative damage in functional senescence has also been investigated, albeit not as comprehensively. Here, we review these investigations. Several studies show that the age-related loss of a number of functions is associated with an accrual of oxidative damage in the tissues mediating those functions. Additionally, treatments that increase the accumulation of oxidative damage with age frequently exacerbate functional losses. Moreover, treatments that reduce the accumulation of oxidative damage often attenuate or delay the loss of function associated with aging. These data provide the foundation for a link between oxidative damage and functional senescence, thereby supporting the oxidative damage hypothesis of aging within the context of age-related functional decline. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:411 / 423
页数:13
相关论文
共 189 条
[1]
Suppression of steroidogenesis and activator protein-1 transcription factor activity in rat adrenals by vitamin E deficiency-induced chronic oxidative stress [J].
Abidi, P ;
Leers-Sucheta, S ;
Azhar, S .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2004, 15 (04) :210-219
[2]
AGING AND PROTEIN OXIDATIVE DAMAGE [J].
AGARWAL, S ;
SOHAL, RS .
MECHANISMS OF AGEING AND DEVELOPMENT, 1994, 75 (01) :11-19
[3]
DNA OXIDATIVE DAMAGE AND LIFE EXPECTANCY IN HOUSEFLIES [J].
AGARWAL, S ;
SOHAL, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) :12332-12335
[4]
Mitochondrial DNA deletion mutations and sarcopenia [J].
Aiken, J ;
Bua, E ;
Cao, ZJ ;
Lopez, M ;
Wanagat, J ;
McKenzie, D ;
McKiernan, S .
INCREASING HEALTHY LIFE SPAN: CONVENTIONAL MEASURES AND SLOWING THE INNATE AGING PROCESS, 2002, 959 :412-423
[5]
Protein oxidation and enzyme activity decline in old brown Norway rats are reduced by dietary restriction [J].
Aksenova, MV ;
Aksenov, MY ;
Carney, JM ;
Butterfield, DA .
MECHANISMS OF AGEING AND DEVELOPMENT, 1998, 100 (02) :157-168
[6]
GENETIC ALTERATION OF NORMAL AGING PROCESSES IS RESPONSIBLE FOR EXTENDED LONGEVITY IN DROSOPHILA [J].
ARKING, R ;
WELLS, RA .
DEVELOPMENTAL GENETICS, 1990, 11 (02) :141-148
[7]
Forward and reverse selection for longevity in Drosophila is characterized by alteration of antioxidant gene expression and oxidative damage patterns [J].
Arking, R ;
Burde, V ;
Graves, K ;
Hari, R ;
Feldman, E ;
Zeevi, A ;
Soliman, S ;
Saraiya, A ;
Buck, S ;
Vettraino, J ;
Sathrasala, K ;
Wehr, N ;
Levine, RL .
EXPERIMENTAL GERONTOLOGY, 2000, 35 (02) :167-185
[8]
Identical longevity phenotypes are characterized by different patterns of gene expression and oxidative damage [J].
Arking, R ;
Burde, V ;
Graves, K ;
Hari, R ;
Feldman, E ;
Zeevi, A ;
Soliman, S ;
Saraiya, A ;
Buck, S ;
Vettraino, J ;
Sathrasala, K .
EXPERIMENTAL GERONTOLOGY, 2000, 35 (03) :353-373
[9]
ARKING R, 1998, BIOL AGING OBSERVATI, V2
[10]
Caloric restriction reduces fiber loss and mitochondrial abnormalities in aged rat muscle [J].
Aspnes, LE ;
Lee, CM ;
Weindruch, R ;
Chung, SS ;
Roecker, EB ;
Aiken, JM .
FASEB JOURNAL, 1997, 11 (07) :573-581