Oxidative state in platelets and erythrocytes in aging and Alzheimer's disease

被引:101
作者
Kawamoto, EM
Munhoz, CD
Glezer, I
Bahia, VS
Caramelli, P
Nitrini, R
Gorjao, R
Curic, R
Scavone, C
Marcourakis, T
机构
[1] Univ Sao Paulo, Sch Med, Neurol Res Lab, Ctr Invest Neurol FMUSP, BR-01246903 Sao Paulo, Brazil
[2] Univ Sao Paulo, Sch Med, Dept Physiol, Inst Biomed Sci, Sao Paulo, Brazil
[3] Univ Sao Paulo, Sch Med, Dept Neurol, Sao Paulo, Brazil
[4] Univ Sao Paulo, Sch Med, Dept Pharmacol, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Alzheimer's disease; aging; platelets; erythrocytes; cyclic GMP; nitric oxide; SOD; TBARS; Na; K-ATPase; oxidative stress;
D O I
10.1016/j.neurobiolaging.2004.08.011
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
Several studies have shown involvement of peroxynitrite anion, a potent oxidative agent, in Alzheimer's disease (AD) neuropathology. Herein, we assessed in platelets and erythrocytes of AD patients, age-matched and young adults controls: thiobarbituric acid-reactive substances (TBARS) production; superoxide dismutase (SOD), nitric oxide synthase (NOS) and Na,K-ATPase activities; cyclic GMP (cGMP) content, both basal and after sodium nitroprusside (SNP) stimulation. Aging was associated with an increase in TBARS production and NOS activity, a decrease in basal cGMP content and no change in SOD and Na,K-ATPase activities. AD patients, compared to aged controls, have: increase in TBARS production and in NOS, SOD and Na,K-ATPase activities but no alteration in basal cGMP content. SNP increased cGMP platelets production in all groups. In conclusion, we demonstrated in platelets and erythrocytes a disruption in systemic modulation of oxidative stress in aging and with more intensity in AD. (c) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:857 / 864
页数:8
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