Effects
Cells were transfected with specific siRNA and then treated with SAM for 24 h. The cells were post-incubated with 1 mM H2O2 for 6 h. The effects of IGF-I and Nrf2 siRNA on SAM-induced cell viability in the presence of H2O2 were measured with an MTT assay (A). All expression levels are presented as the percent increase over the control. ROS generation was measured using DCFH-DA (B). The fluorescent intensity was measured at 530 nm after excitation at 490 nm. Fluorescent levels are expressed as the percent increase over the control, and are expressed as mean ± SD (n=8). Statistical analysis; *p<0.01, and **p < 0.05 vs. control media. # p<0.05 and ## p<0.01 vs. media with H2O2 alone. & p < 0.05 vs. media with SAM and H2O2.
Figure 10: Effects of IGF-I and Nrf2 silencing on SAM-induced cell viability and ROS generation in H2O2-induced apoptosis.