Baicalin attenuates oxygen-glucose deprivation-induced injury by inhibiting oxidative stress-mediated 5-lipoxygenase activation in PC12 cells

被引:33
作者
Li, Cheng-tan [1 ,2 ,3 ]
Zhang, Wei-ping [1 ]
Fang, San-hua [1 ]
Lu, Yun-bi [1 ]
Zhang, Li-hui [2 ,3 ]
Qi, Ling-ling [1 ]
Huang, Xue-qin [1 ]
Huang, Xiao-jia [1 ]
Wei, Er-qing [1 ]
机构
[1] Zhejiang Univ, Dept Pharmacol, Sch Med, Hangzhou 310058, Zhejiang, Peoples R China
[2] Hangzhou Normal Univ, Hangzhou Key Lab Neurobiol, Sch Basic Med, Hangzhou 310036, Zhejiang, Peoples R China
[3] Hangzhou Normal Univ, Dept Pharmacol, Sch Basic Med, Hangzhou 310036, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
baicalin; 5-lipoxygenase; rat pheochromocytoma (PC12) cell; oxygen-glucose deprivation; reactive oxygen species; p38 mitogen-activated protein kinase; FOCAL CEREBRAL-ISCHEMIA; RAT CORTICAL-NEURONS; P38; MAP-KINASES; BRAIN INFLAMMATION; REPERFUSION INJURY; NMDA RECEPTOR; PROTECTS; PATHWAY; DISEASES; CYCLOOXYGENASE;
D O I
10.1038/aps.2009.196
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aim: To determine whether the flavonoid baicalin attenuates oxygen-glucose deprivation (OGD)-induced injury by inhibiting oxidative stress-mediated 5-lipoxygenase (5-LOX) activation in PC12 cells. Methods: The effects of baicalin and the 5-LOX inhibitor zileuton on the changes induced by OGD/recovery or H2O2 (an exogenous reactive oxygen species [ROS]) in green fluorescent protein-5-LOX-transfected PC12 cells were compared. Results: Both baicalin and zileuton attenuated OGD/recovery-and H2O2-induced injury and inhibited OGD/recovery-induced production of 5-LOX metabolites (cysteinyl leukotrienes) in a concentration-dependent manner. However, baicalin did not reduce baseline cysteinyl leukotriene levels. Baicalin also reduced OGD/recovery-induced ROS production and inhibited 5-LOX translocation to the nuclear envelope and p38 phosphorylation induced by OGD/recovery and H2O2. In contrast, zileuton did not show these effects. Conclusion: Baicalin can inhibit 5-LOX activation after ischemic injury, which may partly result from inhibition of the ROS/p38 mitogen-activated protein kinase pathway.
引用
收藏
页码:137 / 144
页数:8
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