Protective effect of 3-butyl-6-bromo-1(3H)-isobenzofuranone on hydrogen peroxide-induced damage in PC12 cells

被引:25
|
作者
Gao, Yuan [1 ]
Zhang, Hong-Wei [1 ]
Qiao, Hai-Ling [1 ]
Wang, Wei [1 ]
Chang, Jun-Biao [1 ]
机构
[1] Zhengzhou Univ, Sch Med, Dept Clin Pharmacol, Zhengzhou 450052, Henan, Peoples R China
关键词
3-butyl-6-bromo-1(3H)-isobenzofuranone; Oxidative stress; ROS; MMP; Ca2(+)](i); Apoptosis; NITRIC-OXIDE SYNTHASE; OXIDATIVE STRESS; APOPTOSIS; BRAIN; PEROXYNITRITE; DEPRIVATION; GLUTATHIONE; SUPEROXIDE; MECHANISM; DOPAMINE;
D O I
10.1016/j.brainres.2010.08.043
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oxidative stress, an imbalance toward the prooxidant side of the prooxidant/antioxidant homeostasis, occurs in several brain neurodegenerative disorders. The protective effect of 3butyl-6-bromo-1(3H)-isobenzofuranone (Br-NBP), a derivative compound of 1-3-n-butylphthalide (NBP), on the hydrogen peroxide(H2O2)- induced oxidative damage was investigated in PC12 cells. Following exposure of the cells to H2O2, there was a significant reduction in cell survival,activities of glutathione peroxidase (GSH-px) and mitochondria membrane potential(MMP), in contrast, the increased levels in the leakage of lactate dehydrogenase (LDH), malondialdehyde (MDA) contents, nitric oxide (NO) productions, intracellular reactive oxygen species (ROS), intracellular Ca2+. concentration ([Ca2+](i)), as well as cell apoptosis were observed. However, pretreatment of cells with Br-NBP prior to H2O2 exposure attenuated all the changes mentioned above in a concentration-dependent manner except no effect on activities of GSH-px. Br-NBP exhibited the protective effect against H2O2-induced cytotoxicity in PC12 cells, suggesting that the compound may be a potential therapeutic agent for diseases induced by oxidative damage. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 247
页数:9
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