Purpose: We investigated the possible effects of 50 and 60 Hz magnetic fields (MFs) on reactive oxygen species (ROS) production, DNA damage, DNA damage repair rate, as well as gene expression related to oxidative stress and DNA damage signaling.
Materials and methods: Human SH-SY5Y neuroblastoma cells were sham-exposed or exposed to 100 µTRMS MFs for 24 h, then assayed or further treated with 100 µM menadione for 1 h before the assay. The levels of ROS and cytosolic superoxide anion (O2•-) were assayed fluorometrically. DNA damage and gene expression were assayed by comet assay and RT-qPCR, respectively. To examine whether MFs affected DNA damage repair rate, cells were allowed to repair their DNA for 1 or 2 h after menadione treatment and then assayed for DNA damage.
Results: There was suggestive evidence of a general low-magnitude increase in the expression of ROS-related genes (primarily genes with antioxidant activity) when quantified immediately after MF exposure, suggesting a response to a small increase in ROS level. The possible upregulation of ROS-related genes is supported by the finding that the level of menadione-induced ROS was consistently decreased by 50 Hz MFs (not significantly by 60 Hz MFs) in several measurements 30-60 min after MF exposure. MF exposures did not affect cytosolic O2•- levels, DNA damage, or its repair rate. Changes in the expression of DNA damage-signaling genes in the MF-exposed cells did not exceed the expected rate of false-positive findings. No firm evidence was found for differential effects from 50 vs. 60 Hz MFs.
Conclusions: While only weak effects were found on the endpoints measured, the results are consistent with MF effects on ROS signaling.
Keywords: DNA damage; DNA repair; Extremely low-frequency magnetic fields; reactive oxygen species (ROS).