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The aim of the present study was to investigate the role of spermidine on the antioxidant activity of hydrogen peroxide (H2O2)-induced apoptosis of macrophage RAW264.7 cells. RAW264.7 cells were cultured with the polyamine spermidine and were exposed to H2O2 for different durations. The level of intracellular reactive oxygen species (ROS) and cellular antioxidant enzyme activity were measured, cell viability was estimated by the MTT assay, and apoptosis rate was determined using a flow cytometric analysis. Treatment of RAW264.7 cells with spermidine led to a significant reduction of intracellular ROS levels and a significant increase of cell viability of RAW264.7 cells treated with H2O2 for 12h compared to cells not treated with spermidine. Treatment of RAW264.7 cells with spermidine reduced apoptosis induced by H2O2 for 12h compared to cells not treated with spermidine. These results suggest that the protective effect of spermidine on H2O2-induced apoptosis may be associated with its free radical scavenging
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