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
相关论文
共 87 条
[51]   Increased peroxidation and reduced antioxidant enzyme activity in Alzheimer's disease [J].
Marcus, DL ;
Thomas, C ;
Rodriguez, C ;
Simberkoff, K ;
Tsai, JS ;
Strafaci, JA ;
Freedman, ML .
EXPERIMENTAL NEUROLOGY, 1998, 150 (01) :40-44
[52]   Amyloid beta-peptide and oxidative cellular injury in Alzheimer's disease [J].
Mark, RJ ;
Blanc, EM ;
Mattson, MP .
MOLECULAR NEUROBIOLOGY, 1996, 12 (03) :211-224
[53]   MACROPHAGE OXIDATION OF L-ARGININE TO NITRITE AND NITRATE - NITRIC-OXIDE IS AN INTERMEDIATE [J].
MARLETTA, MA ;
YOON, PS ;
IYENGAR, R ;
LEAF, CD ;
WISHNOK, JS .
BIOCHEMISTRY, 1988, 27 (24) :8706-8711
[54]   Cellular and molecular mechanisms underlying perturbed energy metabolism and neuronal degeneration in Alzheimer's and Parkinson's diseases [J].
Mattson, MP ;
Pedersen, WA ;
Duan, WZ ;
Culmsee, C ;
Camandola, S .
OXIDATIVE/ENERGY METABOLISM IN NEURODEGENERATIVE DISORDERS, 1999, 893 :154-175
[55]  
MCCORD JM, 1969, J BIOL CHEM, V244, P6056
[56]   NITRIC-OXIDE, CGMP, AND HORMONE REGULATION OF ACTIVE SODIUM-TRANSPORT [J].
MCKEE, M ;
SCAVONE, C ;
NATHANSON, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) :12056-12060
[57]  
MCKHANN G, 1984, NEUROLOGY, V34, P939, DOI 10.1212/WNL.34.7.939
[58]   Effects of free radicals on partial reactions of the Na,K-ATPase [J].
Mense, M ;
Stark, G ;
Apell, HJ .
JOURNAL OF MEMBRANE BIOLOGY, 1997, 156 (01) :63-71
[59]   IMPORTANCE OF SE-GLUTATHIONE PEROXIDASE, CATALASE, AND CU/ZN-SOD FOR CELL-SURVIVAL AGAINST OXIDATIVE STRESS [J].
MICHIELS, C ;
RAES, M ;
TOUSSAINT, O ;
REMACLE, J .
FREE RADICAL BIOLOGY AND MEDICINE, 1994, 17 (03) :235-248
[60]   Diagnostic and Statistical Manual of Mental Disorders [J].
Mittal, Vijay A. ;
Walker, Elaine F. .
PSYCHIATRY RESEARCH, 2011, 189 (01) :158-159