Attenuation of LPS-induced apoptosis in NGF-differentiated PC12 cells via NF-κB pathway and regulation of cellular redox status by an oxazine derivative

被引:35
作者
Ansari, Niloufar [1 ]
Khodagholi, Fariba [1 ]
Amini, Mohsen [2 ,3 ]
Shaerzadeh, Fatemeh [1 ]
机构
[1] Shahid Beheshti Univ Med Sci, Neurosci Res Ctr, Tehran, Iran
[2] Univ Tehran Med Sci, Fac Pharm, Dept Med Chem, Tehran 14176, Iran
[3] Univ Tehran Med Sci, Drug Design & Dev Res Ctr, Tehran 14176, Iran
关键词
Apoptosis; LPS; NF-kappa B; Oxazine derivative; PC12; cells; HEAT-SHOCK-PROTEIN; ALZHEIMERS-DISEASE; NRF2-ARE PATHWAY; OXIDATIVE STRESS; HEME OXYGENASE-1; ACTIVATION; INDUCTION; ANTIOXIDANT; TRANSCRIPTION; SUPEROXIDE;
D O I
10.1016/j.biochi.2011.01.012
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
Neuronal cell death due to apoptosis is a common characteristic of neurodegenerative diseases. In this study, we report protective effect of 2-ethoxy-4,5-diphenyl-1,3-oxazine-6-one (EDPOO) against lipopolysaccharide (LPS)-induced cell death in rat pheochromocytoma (PC12) cells, as assessed by MTT test, acridine orange/ethidium bromide staining, determination of Bax, Bcl-2 and caspase-3 levels. We further show that this compound could increase heat shock proteins Hsp-70 and Hsp-32 levels. EDPOO also modulates nuclear levels of Nrf2 and NF-kappa B, transcription factors that are activated by intracellular reactive oxygen species and/or mediators generated due to chemical exposure of cells. Pretreatment of the cells with this oxazine derivative also increases gamma-GCS level, as well as antioxidant enzyme activities, in a dose-dependent manner. Protective effect of this compound could represent a promising approach for treatment of neurodegenerative diseases. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:899 / 908
页数:10
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