Redox analysis of human plasma allows separation of pro-oxidant events of aging from decline in antioxidant defenses

被引:323
作者
Jones, DP [1 ]
Mody, VC
Carlson, JL
Lynn, MJ
Sternberg, P
机构
[1] Emory Univ, Sch Med, Dept Biochem, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Ophthalmol, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Publ Hlth, Div Biostat, Atlanta, GA 30322 USA
关键词
oxidation-reduction; oxidative stress; glutathione; cysteine; signal transduction; free radicals;
D O I
10.1016/S0891-5849(02)01040-7
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
Oxidative stress is a component of diseases and degenerative processes associated with aging. However, no means are available to assess causative oxidative events separately from decline in function of protective antioxidant systems. Previous studies show that ongoing oxidative processes maintain plasma cysteine/cystine redox at a value that is more oxidized than the antioxidant glutathione/glutathione disulfide (GSH/GSSG) system, suggesting that redox analysis of these plasma thiols could allow separate evaluation of an increase in oxidative events from a decline in antioxidant function. The present study uses measurement of cysteine/cystine and GSH/GSSG redox in plasma of 122 healthy individuals aged 19-85 years to determine whether thiol-disulfide redox changes occur with age. The results show a linear oxidation of cysteine/cystine redox state with age at a rate of 0.16 mV/year over the entire age span. In contrast, GSH/GSSG redox was not oxidized prior to 45 years and subsequently was oxidized at a nearly linear rate of 0.7 mV/year. These data suggest that there is a continuous, linear increase in oxidative events throughout adult life but that the capacity of the GSH antioxidant system is maintained until 45 years and then declines rapidly. The data further suggest that redox states of cysteine/cystine and GSH/GSSG provide an approach to clinically distinguish between increased causative oxidative events and decreased GSH antioxidant function. In principle, such analyses can be used to assess efficacy of intervention strategies against oxidative stress prior to or early after onset of clinical symptoms in aging and age-related disease. (C) 2002 Elsevier Science Inc.
引用
收藏
页码:1290 / 1300
页数:11
相关论文
共 38 条
[1]   Oxidative stress and gene regulation [J].
Allen, RG ;
Tresini, M .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (03) :463-499
[2]   Glutathione therapy: From prodrugs to genes [J].
Anderson, ME ;
Luo, JL .
SEMINARS IN LIVER DISEASE, 1998, 18 (04) :415-424
[3]  
BAUMAN PF, 1998, J NUTR, V118, P1049
[4]   The free radical theory of aging matures [J].
Beckman, KB ;
Ames, BN .
PHYSIOLOGICAL REVIEWS, 1998, 78 (02) :547-581
[5]   Oxidative damage and protection of the RPE [J].
Cai, JY ;
Nelson, KC ;
Wu, M ;
Sternberg, P ;
Jones, DP .
PROGRESS IN RETINAL AND EYE RESEARCH, 2000, 19 (02) :205-221
[6]  
Chevion M, 2000, FREE RADICAL RES, V33, pS99
[7]   Redox modulation of the NMDA receptor [J].
Choi, YB ;
Lipton, SA .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2000, 57 (11) :1535-1541
[8]  
Clark W.M., 1960, OXIDATION REDUCTION
[9]   Antioxidants: Strategies for Interventions in Aging and Age-Related Diseases A Workshop Sponsored by the National Institute on Aging and by the Office of Dietary Supplements [J].
Darley-Usmar, Victor ;
Starke-Reed, Pamela E. .
ANTIOXIDANTS & REDOX SIGNALING, 2000, 2 (03) :375-377
[10]  
Delori FC, 2001, INVEST OPHTH VIS SCI, V42, P1855