Ampelopsin Inhibits H2O2-induced Apoptosis by ERK and Akt Signaling Pathways and Up-regulation of Heme Oxygenase-1

被引:47
作者
Kou, Xianjuan [3 ]
Shen, Keyin [4 ]
An, Yuhui [5 ]
Qi, Shimei
Dai, Wu-Xing [1 ]
Yin, Zhimin [2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Biochem & Mol Biol, Wuhan 430030, Peoples R China
[2] Nanjing Normal Univ, Coll Life Sci, Nanjing 210046, Jiangsu, Peoples R China
[3] Wu Han Inst Phys Educ, Coll Hlth Sci, Wuhan, Peoples R China
[4] Wu Han Inst Phys Educ, Coll Sports Econ & Management, Wuhan, Peoples R China
[5] Zhengzhou Univ, Coll Med, Zhengzhou, Peoples R China
关键词
neuroprotection; ampelopsin; H2O2; heme oxygenase-1; ERK; Akt; RAT GLIOMA-CELLS; OXIDATIVE-STRESS; PC12; CELLS; INDUCED CYTOTOXICITY; PROTEIN EXPRESSION; ACTIVATION; HO-1; FLAVANONES; QUERCETIN; INDUCTION;
D O I
10.1002/ptr.3671
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Oxidative stress plays an important role in neurodegenerative disorders. Ampelopsin, a flavonoid abundant in Rattan tea (Ampelopsis grossedentata), is a potent antioxidant and its neuroprotective effect against H2O2-induced apoptosis in PC12 cells is investigated here for the first time. It was found that treatment of cells with ampelopsin for 1?h significantly reduced the loss of vitality, LDH release and apoptosis and inhibited the formation of reactive oxygen species (ROS). Ampelopsin was able to prevent the activation of p38 induced by H2O2. In addition, up-regulation of heme oxygenase-1 (HO-1) expression by ampelopsin was shown to be both dose- and time-dependent. Mechanically, HO-1 expression induced by ampelopsin was found to be due to activation of the ERK and Akt signaling pathways, because it was almost completely blocked by the specific inhibitors of ERK and Akt. These results suggest that ampelopsin increases cellular antioxidant defense through activation of the ERK and Akt signaling pathways, which induces HO-1 expression and thereby protects PC12 cells from H2O2-induced apoptosis. Copyright (c) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:988 / 994
页数:7
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