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Medical/biological Study (experimental study)Chronic exposure to 50Hz magnetic fields causes a significant weakening of antioxidant defence systems in aged rat brain. med./biol. By: Falone S, Mirabilio A, Carbone MC, Zimmitti V, Di Loreto S, Mariggio MA, Mancinelli R, Di Ilio C, Amicarelli F Published in: Int J Biochem Cell Biol 2008; 40 (12): 2762 - 2770 ( PubMed Entry , Journal web site )Aim of study (according to author) To study whether the ageing process can increase susceptibility towards extremely low frequency magnetic field mediated pro-oxidative stress, differences in the antioxidant defense systems and neurotrophic support (nerve growth factor-related gene expression and protein expression) after chronic exposure were examined in rat brains. Background/further details: 3-months-old femals rats (n=20) and 19-months-old female rats (n=20) were randomly assigned to an exposure group and a control group.
The magnetic flux density (0.1 mT) was the reference level recommended by the European Commission (1999/519/EC) for general public exposure. The experiment was performed 3 times with different rat colonies. Endpoints Exposure General category: magnetic field, 50/60 Hz (AC) | Field characteristics | Parameters |
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50 Hz  exposure duration: continuous for 10 days
| magnetic flux density: 0.1 mT
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FIELD View further expo parametersExposed system: animal (species/strain): rat/Sprague-Dawley whole body exposure Methods Endpoint/Measurement parameters/Methodology - molecular biosynthesis: antioxidant gene expression (mRNA levels of superoxide dismutase (SOD1/2), catalase, selenium-dependent glutathione peroxidase, catalase, glutathione reductase, glutathione-S-transferase, nerve growth factor (NGF), neurotrophic tyrosine kinase receptor type 1 (TrkA); RT-PCR) and protein expression (TrkA and NGF; Western Blot)
- cell function: antioxidant enzymatic activity (superoxide dismutase (SOD1/2), selenium-dependent glutathione peroxidase, catalase, glutathione reductase, glutathione-S-transferase, total protein content; spectrophotometry)
- others: body weight and food intake (before exposure, then every 48 h and after exposure)
investigated material: isolated bio./chem. substance (in vitro), DNA/RNA (in vitro), cortices homogenates and extracts investigation on living organism investigated organ system: brain/CNS
time of investigation: before, during and after exposure
Main outcome of study (according to author) The results showed that exposure to extremely low frequency magnetic fields significantly affected antioxidant enzymatic capacity in both young and aged rats, although in opposite ways. Exposed young rats enhanced their neurotrophic signaling and anti-oxidative enzymatic defense. Aged rats exhibited a significant decrease in all major anti-oxidative enzymatic activities. Food intake and body weight were not affected by exposure.
The data seem to suggest that exposure to extremely low frequency magnetic fields may act as a risk factor for the occurence of oxidative stress-based nervous system pathologies associated with ageing. (Study character: medical/biological study, experimental study, full/main study, blind study)
Study funded by - Agenzia Spaziale Italiana (ASI; Italian Space Agency), Italy
- Ministero dell'Ambiente e della Tutela del Territorio e del Mar (Ministry of Environment and Territory), Italy
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Glossary: 50/60 Hz, AC, animal, antioxidant, biological, biosynthesis, blind study, brain, catalase, cell, chronic exposure, CNS, colonies, control group, cortices, DNA, endpoint, enzymatic, enzymatic activities, exposed, exposure, extracts, extremely low frequency, full/main study, gene expression, glutathione, glutathione peroxidase, glutathione reductase, homogenates, in vitro, kinase, magnetic fields, magnetic flux density, molecular, mRNA, nervous system, NGF, organism, oxidative, oxidative stress, pathologies, protein, protein expression, randomly, rat/Sprague-Dawley, rats, receptor, reference level, risk factor, RNA, RT-PCR, selenium, significant, species, spectrophotometry, strain, superoxide dismutase, tyrosine, Western blot, whole body exposure |
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