Inhibition of ROS-induced apoptosis in endothelial cells by nitrone spin traps via induction of phase II enzymes and suppression of mitochondria-dependent pro-apoptotic signaling

被引:50
作者
Das, Amlan [2 ]
Gopalakrishnan, Bhavani [2 ]
Voss, Oliver H. [3 ,4 ]
Doseff, Andrea I. [3 ,4 ]
Villamena, Frederick A. [1 ,2 ]
机构
[1] Ohio State Univ, Coll Med, Dept Pharmacol, Columbus, OH 43210 USA
[2] Ohio State Univ, Davis Heart & Lung Res Inst, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Mol Genet, Div Pulm Allergy Crit Care & Sleep Med, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Internal Med, Columbus, OH 43210 USA
关键词
Nitrones; Spin traps; Oxidative stress; Endothelial dysfunction; Nrf-2; SUPEROXIDE RADICAL-ANION; N-OXIDE DMPO; HEME OXYGENASE-1 GENE; OXIDATIVE STRESS; NITRIC-OXIDE; NATURAL ANTIOXIDANTS; MOLECULAR-MECHANISMS; INORGANIC RADICALS; EPITHELIAL-CELLS; ACTIVATION;
D O I
10.1016/j.bcp.2012.04.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oxidative stress is the main etiological factor behind the pathogenesis of various diseases including inflammation, cancer, cardiovascular and neurodegenerative disorders. Due to the spin trapping abilities and various pharmacological properties of nitrones, their application as therapeutic agent has been gaining attention. Though the antioxidant properties of the nitrones are well known, the mechanism by which they modulate the cellular defense machinery against oxidative stress is not well investigated and requires further elucidation. Here, we have investigated the mechanisms of cytoprotection of the nitrone spin traps against oxidative stress in bovine aortic endothelial cells (BAEC). Cytoprotective properties of both the cyclic nitrone 5,5-dimethyl-pyrroline N-oxide (DMPO) and linear nitrone alpha-phenyl N-tert-butyl nitrone (PBN) against H2O2-induced cytotoxicity were investigated. Preincubation of BAEC with PBN or DMPO resulted in the inhibition of H2O2-mediated cytotoxicity and apoptosis. Nitrone-treatment resulted in the induction and restoration of phase II antioxidant enzymes via nuclear translocation of NF-E2-related factor 2 (Nrf-2) in oxidatively-challenged cells. Furthermore, the nitrones were found to inhibit the mitochondrial depolarization and subsequent activation of caspase-3 induced by H2O2. Significant down-regulation of the pro-apoptotic proteins p53 and Bax, and up-regulation of the antiapoptotic proteins Bcl-2 and p-Bad were observed when the cells were preincubated with the nitrones prior to H2O2-treatment. It was also observed that Nrf-2 silencing completely abolished the protective effects of nitrones. Hence, these findings suggest that nitrones confer protection to the endothelial cells against oxidative stress by modulating phase II antioxidant enzymes and subsequently inhibiting mitochondria-dependent apoptotic cascade. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:486 / 497
页数:12
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