Peroxynitrite-induced alterations in synaptosomal membrane proteins: Insight into oxidative stress in Alzheimer's disease

被引:147
作者
Koppal, T
Drake, J
Yatin, S
Jordan, B
Varadarajan, S
Bettenhausen, L
Butterfield, DA [1 ]
机构
[1] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
[2] Univ Kentucky, Ctr Membrane Sci, Lexington, KY 40506 USA
[3] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40506 USA
关键词
peroxynitrite; nitric oxide; Alzheimer's disease; protein oxidation; glutathione;
D O I
10.1046/j.1471-4159.1999.0720310.x
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
Peroxynitrite (ONOO-) is a highly reactive, oxidizing anion with a half-life of <1 s that is formed by reaction of superoxide radical anion with nitric oxide. Several reports of ONOO--induced oxidation of lipids, proteins, DNA, sulfhydryls, and inactivation of key enzymes have appeared. ONOO- has also been implicated as playing a role in the pathology of several neurodegenerative disorders, such as Alzheimer's disease (AD) and amyotrophic lateral sclerosis, among others. Continuing our laboratory's interest in free radical oxidative stress in brain cells in AD, the present study was designed to investigate the damage to brain neocortical synaptosomal membrane proteins and the oxidation-sensitive enzyme glutamine synthetase (GS) caused by exposure to ONOO-. These synaptosomal proteins and GS have previously been shown by us and others to have been oxidatively damaged in AD brain and also following treatment of synaptosomes with amyloid beta-peptide. The results of the current study showed that exposure to physiological levels of ONOO- induced significant protein conformational changes, demonstrated using electron paramagnetic resonance in conjunction with a protein-specific spin label, and caused oxidation of proteins, measured by the increase in protein carbonyls. ONOO- also caused inactivation of GS and led to neuronal cell death examined in a hippocampal cell culture system. All these detrimental effects of ONOO- were successfully attenuated by the thiol-containing antioxidant tripeptide glutathione. This research shows that ONOO- can oxidatively modify both membranous and cytosolic proteins, affecting both their physical and chemical nature. These findings are discussed with reference to the potential involvement of ONOO- in AD neurodegeneration.
引用
收藏
页码:310 / 317
页数:8
相关论文
共 63 条
[51]  
Smith MA, 1997, J NEUROSCI, V17, P2653
[52]   Oxidative damage in Alzheimer's [J].
Smith, MA ;
Perry, G ;
Richey, PL ;
Sayre, LM ;
Anderson, VE ;
Beal, MF ;
Kowall, N .
NATURE, 1996, 382 (6587) :120-121
[53]   Decrease in accessible thiols as an index of oxidative damage to membrane proteins [J].
Soszynski, M ;
Bartosz, G .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 23 (03) :463-469
[54]   Effect of peroxynitrite on erythrocytes [J].
Soszynski, M ;
Bartosz, G .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1996, 1291 (02) :107-114
[55]   S-NITROSYLATION OF PROTEINS WITH NITRIC-OXIDE - SYNTHESIS AND CHARACTERIZATION OF BIOLOGICALLY-ACTIVE COMPOUNDS [J].
STAMLER, JS ;
SIMON, DI ;
OSBORNE, JA ;
MULLINS, ME ;
JARAKI, O ;
MICHEL, T ;
SINGEL, DJ ;
LOSCALZO, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (01) :444-448
[56]   AUTOPSY SAMPLES OF ALZHEIMERS CORTEX SHOW INCREASED PEROXIDATION INVITRO [J].
SUBBARAO, KV ;
RICHARDSON, JS ;
ANG, LC .
JOURNAL OF NEUROCHEMISTRY, 1990, 55 (01) :342-345
[57]  
SUBRAMANIAM R, 1998, IN PRESS NEUROCHEM R
[58]   The possible role of peroxynitrite in Alzheimer's disease: A simple hypothesis that could be tested more thoroughly [J].
VanDyke, K .
MEDICAL HYPOTHESES, 1997, 48 (05) :375-380
[59]   Modulation of nitric oxide production in human macrophages by apolipoprotein-E and amyloid-beta peptide [J].
Vitek, MP ;
Snell, J ;
Dawson, H ;
Colton, CA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 240 (02) :391-394
[60]   NITRIC OXIDE-INDUCED CYTOTOXICITY - INVOLVEMENT OF CELLULAR-RESISTANCE TO OXIDATIVE STRESS AND THE ROLE OF GLUTATHIONE IN PROTECTION [J].
WALKER, MW ;
KINTER, MT ;
ROBERTS, RJ ;
SPITZ, DR .
PEDIATRIC RESEARCH, 1995, 37 (01) :41-49