3-O-demethylswertipunicoside inhibits MPP+-induced oxidative stress and apoptosis in PC12 cells

被引:12
|
作者
Zhou, Junjun [1 ,2 ]
Sun, Yi [1 ,2 ]
Zhao, Xin [1 ,2 ]
Deng, Zheng [1 ,2 ]
Pu, Xiaoping [1 ,2 ]
机构
[1] Peking Univ, Natl Key Res Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
[2] Peking Univ, Sch Pharmaceut Sci, Dept Mol & Cellular Pharmacol, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
3-O-Demethylswertipunicoside; 1-Methyl-4-phenylpyridinium; Oxidative stress; Apoptosis; Parkinson's disease; PC12; cells; PARKINSON-DISEASE; HUMAN NEUROBLASTOMA; REACTIVE OXYGEN; TOXICITY; MITOCHONDRIA; PATHOGENESIS; ANTIOXIDANT; MECHANISMS; INCREASES; FAMILY;
D O I
10.1016/j.brainres.2013.02.049
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The 3-O-demethylswertipunicoside (3-ODS) is extracted from Swertia punicea. Recent study from our laboratory has demonstrated that the 3-ODS protects against oxidative toxicity and apoptosis in PC12 cells (Zhang, S.P., Du, X.G., Pu, X.P., 2010. Biol. Pharm. Bull. 33, 1529-1533). The aim of our study is to further investigate the neuroprotective mechanisms of 3-ODS in 1-methyl-4-phenylpyridinium (MPP+)-induced neurotoxicity in PC12 cells. The results indicated that pre-treatment with 3-ODS significantly increased the cell viability compared with MPP+ treatment. It also alleviated the oxidative stress by increasing superoxide dismutase (SOD) activity and decreasing malondialdehyde (MDA) level and reactive oxygen specise (ROS) production. Moreover, 3-ODS also attenuated MPP+-induced apoptosis by inhibiting Bax and Bcl-2 expressions, activating caspase-9, caspase-3, poly (ADP-ribose) polymerase-1 (PARP-1) cleavage, apoptosis-inducing factor (AIF) translocation and alpha-synuclein expression. These results suggest that 3-ODS might has applications as a complementary medicine for the treatment of Parkinson's disease (PD) or other neurodegenerative diseases. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 62
页数:10
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