Skip to main content
Fig. 7 | Molecular Brain

Fig. 7

From: Role of miR-326 in neonatal hypoxic-ischemic brain damage pathogenesis through targeting of the δ-opioid receptor

Fig. 7

Effects of miRNA-326 on cell apoptosis under OGD. (a) The cell apoptosis rate did not change immediately at 0 h after OGD (nP > 0.05). Apoptosis was significantly increased in PC12 cells transfected with miR-326 mimics and was significantly decreased in PC12 cells transfected with miR-326 inhibitor at 2 h, 6 h and 12 h after OGD (**P < 0.01; ***P < 0.005; ****P < 0.001). In PC12 cells cotransfected with shDOR and miR-326 inhibitor, the cell apoptosis rate that resulted from the miR-326 inhibitor was partially rescued (**P < 0.01; ***P < 0.005). (b) Overexpression of miR-326 increased the expression levels of Caspase-3 and Bax and decreased Bcl-2 at 2 h, 6 h and 12 h after OGD but not at 0 h (nP > 0.05; **P < 0.01; ***P < 0.005; ****P < 0.001). Inhibition of miR-326 had opposite effects, which were rescued by cotransfection of miR-326 and DOR inhibitors (*P < 0.05; **P < 0.01; ***P < 0.005; ****P < 0.001)

Back to article page