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Published on: July 8, 2016
Genomic instability induced by 50Hz magnetic fields is a dynamically evolving process not blocked by antioxidant
Kavindra Kumar Kesari1, Jukka Luukkonen1, Jukka Juutilainen1
1Department of Environmental Science, University of Eastern Finland, P.O. Box 1627, FI-70211 Kuopio, Finland.
Abstract:
Increased level of micronuclei was observed in SH-SY5Y cells in a previous study at 8 and 15 days after exposure to extremely low frequency (ELF) magnetic fields (MF), indicating possible induction of genomic instability in the progeny of the exposed cells. The aim of this study was to further explore the induction of genomic instability by ELF MFs by increasing the follow-up time up to 45 days after exposure. Human SH-SY5Y neuroblastoma cells were exposed to a 50Hz, 100μT MF for 24h with or without co-exposure to menadione (MQ), a chemical agent that increases cellular superoxide production. Micronuclei, reactive oxygen species (ROS) and lipid peroxidation (LPO) were measured at 15, 30 and 45 days after exposure. To study the possible causal role of ROS in the delayed effects of MF, the antioxidant N-acetylcysteine (NAC) was administered before MF exposure. Consistently with the previous study, the level of micronuclei was statistically significantly elevated 15 days after exposure. A similar effect was observed at 30 days, but not at 45 days after exposure. The level of LPO was statically significantly decreased 30 and 45 days after exposure. Consistently with our previous findings, the MF effect did not depend on co-exposure to MQ. Treatment with NAC effectively decreased cellular ROS level and suppressed the effect of MQ on ROS, but it did not block the MF effect, indicating that increase in ROS is not needed as a causal link between MF exposure and induction of delayed effects. The results presented here are consistent with genomic instability that persists in the progeny of MF-exposed cells up to at least 30 days after exposure. Changes in LPO observed at 30 and 45 days after exposure indicates that the MF-initiated process may continue up to at least 45 days after exposure.
Insights
Extremely low frequency magnetic fields (ELF-MF) exposure may induce genomic instability in cells, persisting for at least 30 days. This study found ELF-MF effects on cell health markers, but not solely through reactive oxygen species.
Area of Science:
- Cellular and Molecular Biology
- Environmental Health
- Genetics and Genomics
Background:
- Previous studies indicated extremely low frequency magnetic fields (ELF-MF) may induce genomic instability.
- Genomic instability was observed in SH-SY5Y cells 8 and 15 days post-exposure.
Purpose of the Study:
- To investigate the long-term effects of ELF-MF exposure on genomic instability.
- To determine the role of reactive oxygen species (ROS) in ELF-MF-induced delayed cellular effects.
Main Methods:
- SH-SY5Y neuroblastoma cells were exposed to 50Hz, 100μT MF for 24 hours.
- Micronuclei, ROS, and lipid peroxidation (LPO) were assessed at 15, 30, and 45 days post-exposure.
- The antioxidant N-acetylcysteine (NAC) was used to probe the involvement of ROS.
Main Results:
- Micronuclei levels were significantly elevated at 15 and 30 days post-exposure, but not at 45 days.
- Lipid peroxidation (LPO) levels decreased significantly at 30 and 45 days post-exposure.
- NAC treatment did not prevent the ELF-MF effect on micronuclei, suggesting ROS are not the primary causal link.
Conclusions:
- ELF-MF exposure can induce a delayed genomic instability in the progeny of exposed cells, persisting for at least 30 days.
- The observed effects are not solely mediated by increased ROS, indicating other mechanisms may be involved.
- ELF-MF exposure initiates a process that influences cellular health markers for at least 45 days.
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