Neuroprotection of taurine against reactive oxygen species is associated with inhibiting NADPH oxidases

被引:35
作者
Han, Zhou [1 ]
Gao, Li-Yan [1 ]
Lin, Yu-Hui [1 ]
Chang, Lei [1 ,2 ]
Wu, Hai-Yin [1 ,2 ]
Luo, Chun-Xia [1 ,2 ]
Zhu, Dong-Ya [1 ,2 ,3 ]
机构
[1] Nanjing Med Univ, Sch Pharm, Dept Pharmacol, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Key Lab Cardiovasc Dis & Mol Intervent, Lab Cerebrovasc Dis, Nanjing 210029, Jiangsu, Peoples R China
[3] Key Lab Human Funct Genom Jiangsu Prov, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Taurine; NMDA; Reactive oxygen species; NADPH oxidase; Calcium; NMDA RECEPTOR; OXIDATIVE STRESS; FREE-RADICALS; NOX FAMILY; SUPEROXIDE; GLUTAMATE; STROKE; MECHANISMS; ISCHEMIA; BRAIN;
D O I
10.1016/j.ejphar.2016.03.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
It is well established that taurine shows potent protection against glutamate-induced injury to neurons in stroke. The neuroprotection may result from multiple mechanisms. Increasing evidences suggest that NADPH oxidases (Nox), the primary source of superoxide induced by N-methyl-D-aspartate (NMDA) receptor activation, are involved in the process of oxidative stress. We found that 100 mu M NMDA induced oxidative stress by increasing the reactive oxygen species level, which contributed to the cell death, in vitro. Neuron cultures pretreated with 25 mM taurine showed lower percentage of death cells and declined reactive oxygen species level. Moreover, taurine attenuated Nox2/Nox4 protein expression and enzyme activity and declined intracellular calcium intensity during NMDA-induced neuron injury. Additionally, taurine also showed neuroprotection against H2O2-induced injury, accompanying with Nox inhibition. So, we suppose that protection of taurine against reactive oxygen species during NMDA-induced neuron injury is associated with Nox inhibition, probably in a calcium-dependent manner. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 135
页数:7
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