1. Mobile phone radiation-induced free radical damage in the liver is inhibited by the antioxidants N-acetyl cysteine and epigallocatechin-gallate.
- Author
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Ozgur E, Güler G, and Seyhan N
- Subjects
- Animals, Catechin pharmacology, Free Radicals metabolism, Free Radicals radiation effects, Glutathione Peroxidase, Guinea Pigs, Liver enzymology, Liver metabolism, Liver radiation effects, Male, Malondialdehyde, Nitric Oxide, Oxidative Stress physiology, Oxidative Stress radiation effects, Peroxidase, Superoxide Dismutase, Time Factors, Acetylcysteine pharmacology, Antioxidants pharmacology, Catechin analogs & derivatives, Cell Phone, Electromagnetic Fields adverse effects, Liver drug effects, Oxidative Stress drug effects
- Abstract
Purpose: To investigate oxidative damage and antioxidant enzyme status in the liver of guinea pigs exposed to mobile phone-like radiofrequency radiation (RFR) and the potential protective effects of N-acetyl cysteine (NAC) and epigallocatechin-gallate (EGCG) on the oxidative damage., Materials and Methods: Nine groups of guinea pigs were used to study the effects of exposure to an 1800-MHz Global System for Mobile Communications (GSM)-modulated signal (average whole body Specific Absorption Rate (SAR) of 0.38 W/kg, 10 or 20 min per day for seven days) and treatment with antioxidants., Results: Significant increases in malondialdehyde (MDA) and total nitric oxide (NO(x)) levels and decreases in activities of superoxide dismutase (SOD), myeloperoxidase (MPO) and glutathione peroxidase (GSH-Px) were observed in the liver of guinea pigs after RFR exposure. Only NAC treatment induces increase in hepatic GSH-Px activities, whereas EGCG treatment alone attenuated MDA level. Extent of oxidative damage was found to be proportional to the duration of exposure (P < 0.05)., Conclusion: Mobile phone-like radiation induces oxidative damage and changes the activities of antioxidant enzymes in the liver. The adverse effect of RFR may be related to the duration of mobile phone use. NAC and EGCG protect the liver tissue against the RFR-induced oxidative damage and enhance antioxidant enzyme activities.
- Published
- 2010
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