Research Article
Tanshinone IIA Pretreatment Protects H9c2 Cells against Anoxia/Reoxygenation Injury: Involvement of the Translocation of Bcl-2 to Mitochondria Mediated by 14-3-3η
Figure 5
Inhibiting mitochondrial translocation of Bcl-2 by silencing 14-3-3η expression abolished the cardioprotective effect of Tanshinone IIA (TSN) pretreatment on the generation of reactive oxygen species (ROS) and oxidative stress in H9c2 cells subjected to anoxia/reoxygenation (A/R) injury. TSN pretreatment inhibited the generation of ROS, and this effect was reversed by AD14-3-3η RNAi. (a) Flow cytometric histograms of 7-dichlorofluorescein. (b) Column bar graph of cell fluorescence for DCF. Values are presented as the for five individual experiments. (A) versus control group; (B) versus A/R group; (C) versus TSN + A/R group; (D) versus AD14-3-3ηRNAi group.
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