Metformin protects PC12 cells against oxygen-glucose deprivation/reperfusion injury

被引:10
作者
Alizadeh, Elnaz Mohammad [1 ]
Mahdavi, Majid [2 ]
Fard, Forough Jenani [1 ]
Chamani, Solmaz [1 ]
Farajdokht, Fereshteh [3 ]
Karimi, Pouran [3 ]
机构
[1] Higher Educ Inst Rab Rashid, Tabriz, Iran
[2] Univ Tabriz, Dept Biol, Tabriz, Iran
[3] Tabriz Univ Med Sci, Neurosci Res Ctr NSRC, Golgasht Ave, Tabriz, Iran
关键词
Oxygen-glucose deprivation; reperfusion injury; ROS; apoptosis; metformin; PERMEABILITY TRANSITION PORE; ISCHEMIA-REPERFUSION INJURY; CEREBRAL-ISCHEMIA; OXIDATIVE STRESS; SIGNALING PATHWAYS; CYTOCHROME-C; ISCHEMIA/REPERFUSION INJURY; CASPASE ACTIVATION; CORTICAL-NEURONS; BAX EXPRESSION;
D O I
10.1080/15376516.2018.1486495
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Oxidative stress has a causative role in ischemic reperfusion-induced cell death. Evidence has shown that metformin is capable to reduce ischemic reperfusion injuries. The current study investigated the effect of metformin on ischemia/reperfusion-induced apoptosis in PC12 cells by evaluation of Bcl-2 family proteins expression. Cells were exposed to a time-dependent in vitro oxygen-glucose deprivation/reoxygenation (OGD/R) injury and then treated with metformin. The intracellular reactive oxygen species (ROS) levels were measured. Western blotting was used to examine the expression of anti- and pro-apoptotic proteins. Moreover, the number of apoptotic cell death was evaluated by TUNEL assay. Our results showed that metformin attenuated ROS generation, downregulated pro-apoptotic BAX expression, and upregulated expression of the Bcl-2 protein in the PC12 cells. Moreover, metformin reduced cell death under OGD/R condition which was confirmed by lower apoptotic cell death in the TUNEL assay. These findings suggest that neuroprotective effect of metformin on OGD/R-induced cell death is possibly mediated by inhibition of ROS-induced apoptosis pathway.
引用
收藏
页码:622 / 629
页数:8
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