Influence of a static magnetic field (250 mT) on the antioxidant response and DNA integrity in THP1 cells

Salem Amara(Yahoo (United Kingdom)), Thierry Douki(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Jean‐Luc Ravanat(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Catherine Garrel(Centre Hospitalier Universitaire de Grenoble), Pascale Guiraud(Centre Hospitalier Universitaire de Grenoble), Alain Favier(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Mohsen Sakly(University of Carthage), Khémaïs Ben Rhouma(University of Carthage), Hafedh Abdelmelek(University of Carthage)
Physics in Medicine and Biology
January 22, 2007
Cited by 46

Abstract

The aim of this study was to investigate the effect of static magnetic field (SMF) exposure in antioxidant enzyme activity, the labile zinc fraction and DNA damage in THP1 cells (monocyte line). Cell culture flasks were exposed to SMF (250 mT) during 1 h (group 1), 2 h (group 2) and 3 h (group 3). Our results showed that cell viability was slightly lower in SMF-exposed groups compared to a sham exposed group. However, SMF exposure failed to alter malondialdehyde (MDA) concentration (+6%, p>0.05) and glutathione peroxidase (GPx) (-5%, p>0.05), catalase (CAT) (-6%, p>0.05) and superoxide dismutase (SOD) activities (+38%, p>0.05) in group 3 compared to the sham exposed group. DNA analysis by single cell gel electrophoresis (comet assay) revealed that SMF exposure did not exert any DNA damage in groups 1 and 2. However, it induced a low level of DNA single strand breaks in cells of group 3. To further explore the oxidative DNA damage, cellular DNA for group 3 was isolated, hydrolyzed and analysed by HPLC-EC. The level of 8-oxodGuo in this group remained unchanged compared to the sham exposed group (+6.5%, p>0.05). Cells stained with zinc-specific fluorescent probes zinpyr-1 showed a decrease of labile zinc fraction in all groups exposed to SMF. Our data showed that SMF exposure (250 mT, during 3 h) did not cause oxidative stress and DNA damage in THP1 cells. However, SMF could alter the intracellular labile zinc fraction.


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