Koppal T, Drake J, Yatin S, Jordan B, Varadarajan S, Bettenhausen L, Butterfield D A
Department of Chemistry, Center of Membrane Sciences, University of Kentucky, Lexington 40506-0055, USA.
J Neurochem. 1999 Jan;72(1):310-7. doi: 10.1046/j.1471-4159.1999.0720310.x.
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.
过氧亚硝酸根离子(ONOO⁻)是一种具有高反应活性的氧化阴离子,半衰期小于1秒,它由超氧阴离子自由基与一氧化氮反应生成。已有多篇报道称ONOO⁻可诱导脂质、蛋白质、DNA、巯基发生氧化反应,并使关键酶失活。ONOO⁻还被认为在多种神经退行性疾病(如阿尔茨海默病(AD)和肌萎缩侧索硬化症等)的病理过程中发挥作用。延续我们实验室对AD患者脑细胞中自由基氧化应激的研究兴趣,本研究旨在探究暴露于ONOO⁻对脑新皮质突触体膜蛋白以及氧化敏感酶谷氨酰胺合成酶(GS)的损伤。我们和其他研究人员之前已经证明,这些突触体蛋白和GS在AD脑以及用淀粉样β肽处理突触体后会发生氧化损伤。本研究结果表明,暴露于生理水平的ONOO⁻会导致显著的蛋白质构象变化(通过电子顺磁共振结合蛋白质特异性自旋标记来证明),并引起蛋白质氧化(通过蛋白质羰基含量的增加来测定)。ONOO⁻还会导致GS失活,并在海马细胞培养系统中导致神经元细胞死亡。含硫醇的抗氧化三肽谷胱甘肽成功减轻了ONOO⁻的所有这些有害影响。这项研究表明,ONOO⁻可以氧化修饰膜蛋白和胞质蛋白,影响它们的物理和化学性质。本文结合ONOO⁻在AD神经退行性变中的潜在作用对这些发现进行了讨论。