Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2014 Feb 19;9(2):e88921.
doi: 10.1371/journal.pone.0088921. eCollection 2014.

Extremely low frequency magnetic field (50 Hz, 0.5 mT) reduces oxidative stress in the brain of gerbils submitted to global cerebral ischemia

Affiliations

Extremely low frequency magnetic field (50 Hz, 0.5 mT) reduces oxidative stress in the brain of gerbils submitted to global cerebral ischemia

Snežana Rauš Balind et al. PLoS One. .

Abstract

Magnetic field as ecological factor has influence on all living beings. The aim of this study was to determine if extremely low frequency magnetic field (ELF-MF, 50 Hz, 0.5 mT) affects oxidative stress in the brain of gerbils submitted to 10-min global cerebral ischemia. After occlusion of both carotid arteries, 3-month-old gerbils were continuously exposed to ELF-MF for 7 days. Nitric oxide and superoxide anion production, superoxide dismutase activity and index of lipid peroxidation were examined in the forebrain cortex, striatum and hippocampus on the 7(th) (immediate effect of ELF-MF) and 14(th) day after reperfusion (delayed effect of ELF-MF). Ischemia per se increased oxidative stress in the brain on the 7(th) and 14(th) day after reperfusion. ELF-MF also increased oxidative stress, but to a greater extent than ischemia, only immediately after cessation of exposure. Ischemic gerbils exposed to ELF-MF had increased oxidative stress parameters on the 7(th) day after reperfusion, but to a lesser extent than ischemic or ELF-MF-exposed animals. On the 14(th) day after reperfusion, oxidative stress parameters in the brain of these gerbils were mostly at the control levels. Applied ELF-MF decreases oxidative stress induced by global cerebral ischemia and thereby reduces possible negative consequences which free radical species could have in the brain. The results presented here indicate a beneficial effect of ELF-MF (50 Hz, 0.5 mT) in the model of global cerebral ischemia.

PubMed Disclaimer

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. ELF-MF effect on NO content in the brain of gerbils submitted to global cerebral ischemia.
Each bar represents mean ± SEM (n = 6–8 animals per group). **p<0.01 and ***p<0.001 indicate significant differences compared to ELF-MF; p<0.05 and ♦♦♦p<0.001 indicate significant differences compared to Ischemia (one-way analysis of variance followed by LSD test).
Figure 2
Figure 2. ELF-MF effect on O2 content in the brain of gerbils submitted to global cerebral ischemia.
Each bar represents mean ± SEM (n = 6–8 animals per group). **p<0.01 and ***p<0.001 indicate significant differences compared to ELF-MF; p<0.05, ♦♦p<0.01 and ♦♦♦p<0.001 indicate significant differences compared to Ischemia (one-way analysis of variance followed by LSD test).
Figure 3
Figure 3. ELF-MF effect on ILP in the brain of gerbils submitted to global cerebral ischemia.
Each bar represents mean ± SEM (n = 6–8 animals per group). *p<0.05, **p<0.01 and ***p<0.001 indicate significant differences compared to ELF-MF; p<0.05 and ♦♦p<0.01 indicate significant differences compared to Ischemia (one-way analysis of variance followed by LSD test).
Figure 4
Figure 4. ELF-MF effect on SOD activity in the brain of gerbils submitted to global cerebral ischemia.
Each bar represents mean ± SEM (n = 6–8 animals per group). **p<0.01 and ***p<0.001 indicate significant differences compared to ELF-MF; ♦♦♦p<0.001 indicates significant differences compared to Ischemia (one-way analysis of variance followed by LSD test).

Similar articles

Cited by

References

    1. Nita DA, Nita V, Spulber S, Moldovan M, Popa DP, et al. (2001) Oxidative damage following cerebral ischemia depends on reperfusion - a biochemical study in rat. J Cell Mol Med 5: 163–170. - PMC - PubMed
    1. Lewén A, Matz P, Chan PH (2000) Free radical pathways in CNS injury. J Neurotrauma 17: 871–890. - PubMed
    1. Chan PH (2001) Reactive oxygen radicals in signaling and damage in the ischemic brain. J Cereb Blood Flow Metab 21: 2–14. - PubMed
    1. Sugawara T, Chan PH (2003) Reactive oxygen radicals and pathogenesis of neuronal death after cerebral ischemia. Antioxid Redox Signal 5: 597–607. - PubMed
    1. Sies H (1993) Strategies of antioxidant defense. Eur J Biochem 215: 213–219. - PubMed

Publication types

Grants and funding

This study was supported by a grant of the Ministry of Education, Science and Technological Development of the Republic of Serbia (Grant No. 173027) and MMA Grant (MFVMA/7/12-14). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

LinkOut - more resources