Shirai T et al. · 2005
A 1.439 GHz TDMA signal was used for exposure of the rat head starting from 5 weeks of age, 90 min a day, 5 days a week, for 104 weeks. Brain tumorigenesis was initiated by an intrauterine exposure to N-ethylnitrosourea (ENU) on gestational day 18. No increase in the incidences or numbers per group of brain and/or spinal cord tumors, either in the males or females, was detected in the EMF exposed groups. There were no inter-group differences in body weights, food consumption, and survival rates.
Lee JS, Huang TQ, Lee JJ, Pack JK, Jang JJ, Seo JS. · 2005
Researchers exposed eight-week-old hsp70.1-deficient mice twice daily for 45 minutes with a 15-minute interval, five days a week for ten weeks at a whole-body average specific absorption rate of 0.4 W/Kg for both 849 MHz and 1763 MHz fields. They examined major tissues histopathologically, assessed cell proliferative activity immunocytochemically, measured apoptosis with a TUNEL assay, and evaluated heat shock protein expression and stress-activated kinase phosphorylation by western blot. No histopathological differences were found between sham- and RF-exposed mice, and there was no evidence of increased proliferative or apoptotic activity. Levels of HSP90, HSP70, and HSP25 showed no obvious changes, and RF exposure did not affect phosphorylation of ERK1/2, JNK1/2, or p38 MAPK.
Komatsubara Y et al. · 2005
Researchers exposed murine m5S cells to 2.45 GHz high-frequency electromagnetic fields for 2 hours at SARs of 5, 10, 20, 50, and 100 W/kg continuous wave and at a mean SAR of 100 W/kg pulse wave with a maximum of 900 W/kg. The effects were compared with sham-exposed controls and with mitomycin C and X-ray treatments as positive controls. No significant differences in chromosomal aberrations were observed between HFEMF-exposed cells and sham controls, while positive controls increased chromatid-type and chromosome-type aberrations.
Huang TQ, Lee JS, Kim TH, Pack JK, Jang JJ, Seo JS. · 2005
The study used 80 male ICR mice initiated with DMBA and then exposed to 849 MHz or 1,763 MHz RF radiation at 0.4 W/kg SAR for 19 weeks. No skin tumors were observed in the sham or RF-exposed groups, while the TPA positive control group had a 95% tumor incidence. Pathological examination and PCNA staining showed no differences between sham and RF-exposed groups, and cyclin D1 and c-fos expression was only detected in TPA-induced tumors. The researchers concluded that RF radiation does not act as a tumor promoter for skin tumors in this model.
Hata K et al. · 2005
The study aimed to clarify the effects of short-term 1439 MHz TDMA exposure on melatonin synthesis in rats. Researchers investigated 208 male and female rats with brain SAR of 7.5 W/kg and whole-body SAR of 1.9 to 2.0 W/kg. After a 12-hour light-dark cycle, serum and pineal melatonin and pineal serotonin were measured by radioimmunoassay in darkness. No significant differences in melatonin or serotonin levels were found between exposed, sham, and cage control groups.
Green AC et al. · 2005
Intracellular calcium concentration ([Ca(2 +) ](i)) was measured in cultured rat cerebellar granule cells and cardiac myocytes during exposure to TETRA fields (380.8875 MHz pulse modulated at 17.6 Hz, 25% duty cycle). Granule cells exposed at specific absorption rates (SARs) of 5, 10, 20, 50 or 400 mW x kg(-1) showed no significant changes in resting [Ca(2 +) ](i). Exposure to TETRA (50 or 400 mW x kg(-1)) had no significant effect on either the rate or amplitude of spontaneous Ca(2 +) transients in cardiac myocytes. Overall, these results showed no evidence of any consistent or biologically relevant effect of TETRA fields on [Ca(2 + )](i) in granule cells and cardiac myocytes at any of the SAR tested.
Gorlitz BD et al. · 2005
Galloni P et al. · 2005
Researchers divided 48 Sprague-Dawley rats into exposed and sham-exposed groups. The rats were exposed 2 h/day, 5 days/week for 4 weeks at a local SAR of 2 W/kg in the ear. Distortion product otoacoustic emissions tests were carried out before, during, and after the exposure. The analysis showed no statistically significant differences in audiological signals between the different groups.
Galloni P et al. · 2005
Researchers evaluated possible effects of cellular phone-like electromagnetic fields on the functionality of the rat cochlea. Distortion product otoacoustic emission amplitude was used as an indicator of outer hair cell status, and multiple exposure protocols with varying frequencies, intensities, and durations were tested before, during, and after exposure. No significant variation due to microwave exposure was evidenced.
Cosquer B, Kuster N, Cassel JC. · 2005
Researchers investigated whether whole-body exposure to 2.45GHz electromagnetic fields alters performance in a 12-arm radial-maze with reduced access to spatial cues in rats. The results showed that microwave exposure as used in the study did not alter spatial working memory when access to spatial cues was reduced. In a replication attempt using a maze apparatus bordered by 30 cm high opaque walls, the performance of exposed rats was normal.
Cosquer B, Galani R, Kuster N, Cassel JC. · 2005
In a first phase, researchers validated the elevated plus-maze apparatus in male Sprague-Dawley rats. They tested anxiety responses at light intensities of 200, 30, 10, and 2.5 lux and with diazepam doses of 0.5 and 1.0 mg/kg. Anxiety responses decreased with decreasing light intensity and were attenuated by diazepam. A separate group of rats was then exposed to 2.45 GHz EMFs with a whole-body SAR of 0.6 W/kg and brain-averaged SAR of 0.9 W/kg for 45 min. EMF exposure did not significantly affect anxiety responses at either low or high ambient light intensity.
Harakawa S et al. · 2005
The effects of exposure to extremely low frequency electric fields (ELF EFs) on plasma lipid peroxide levels and antioxidant activity (AOA) in Sprague–Dawley rats were studied. The test compared rats treated with a combination of the oxidizing agent AAPH and a 50 Hz EF of 17.5 kV/m for 15 min per day for 7 days, as well as AAPH alone, EF alone, or no treatment. EF significantly decreased the plasma peroxide level in rats treated with AAPH, similar to treatment by ascorbic acid or the superoxide dismutase.
Barcal J, Cendelín J, Vozeh F, Zalud V. · 2005
Researchers performed direct registration of brain cortical and hippocampal activity during high-frequency electromagnetic field exposure. Experiments used urethane anaesthesia in Lurcher mutant mice with wild type littermates as controls. Animals were exposed to HF EMF with frequency corresponding to cellular phones. ECoG evaluation showed a distinct shift to lower frequency components in healthy mice but only gentle differences in Lurcher mutant mice. Hippocampal rhythmicity showed gentle changes with increase of higher frequencies and changes in theta oscillations in both animal types.
Anghileri LJ, Mayayo E, Domingo JL, Thouvenot P. · 2005
Mice were treated with 1 hour per week of radiofrequency exposure for 4 months while a sham-exposed group served as controls. The evolution of carcinogenesis was followed up to 18 months, and the maximal life span of control mice was about 24 months. All dead animals were clinically and histologically examined to give an age-determined comparative quantification of the evolving carcinogenesis. A radiocalcium tracer method permitted the evaluation of radiofrequency effects on transmembrane transport of extracellular calcium at 1 and 24 hours after exposure, and the determination of induced lipid peroxidation completed this second study.
Ozguner F et al. · 2005
The study compared the protective effects of melatonin and CAPE against 900 MHz mobile phone radiation-induced renal tubular injury in rats. Exposure increased urinary NAG and renal MDA levels in rats. Both melatonin and CAPE significantly reduced these elevated markers. Melatonin also increased SOD and GSH-Px activities above control levels, while CAPE did not increase these enzymes.
Ozguner F, Oktem F, Ayata A, Koyu A, Yilmaz HR. · 2005
Wang Q, Cao ZJ, Bai XT. · 2005
Researchers exposed cerebral cortical neurons from postnatal rats to 900 MHz continuous microwave EMF with a SAR of 1.15 to 3.22 mW/g for 2 hours per day over 6 consecutive days and for 12 hours at one time. GABA receptor was selected as the biological endpoint. Significant changes in GABA receptor expression were observed in exposed neurons (P < 0.01), and the expression was significantly regulated by the microwave with a power window effect.
Trosic I, Busljeta I. · 2005
Researchers exposed Wistar rats to 2.45 GHz continuous RF/MW radiation for 2 hours daily, 7 days a week, at 5–10 mW/cm², with subgroups receiving 4, 16, 30, and 60 total hours of exposure. The frequency of micronucleated bone marrow erythrocytes was significantly increased after 15 irradiation treatments. No statistically significant differences in micronucleus frequency were observed after 2, 8, or 30 irradiation treatments.
Seaman RL, Phelix CF. · 2005
3-NP significantly increased ER intracisternal width, ER area density, and nuclear envelope thickness. Microwave exposure at 6 W/kg alone also significantly increased these measures. Exposure of 3-NP-treated animals at 0.6 W/kg reduced the effects of 3-NP.
Nikolova T et al. · 2005
ELF-EMF significantly affected transcript levels of bcl-2, bax, and GADD45 genes but did not affect neural-specific gene mRNA levels. RF-EMF down-regulated neural-specific Nurr1 and up-regulated bax and GADD45 mRNA levels. Short-term RF-EMF exposure for 6 hours caused a transient increase in DNA double-strand breaks, while 48-hour exposure did not. No effects were observed on mitochondrial function, nuclear apoptosis, cell proliferation, or chromosomal alterations.
Finnie JW. · 2005
Researchers exposed mice to 900 MHz radiofrequency fields using a purpose-designed exposure system, giving each animal a single, far-field, whole body exposure at a specific absorption rate of 4 W/kg. The study measured activation of the immediate early gene c-fos in mouse brain tissue after this acute exposure. Activation of c-fos in exposed and sham-exposed brains was comparable, but was greatly increased compared with freely moving controls. The results suggest that the majority of the acute genomic response detected by c-fos expression was due to immobilisation.
Ebert S et al. · 2005
This study determined the thermal regulatory and thermal breakdown thresholds for in-tube restrained B6C3F1 and NMRI mice exposed to radiofrequency electromagnetic fields at 905 MHz. The thermal regulatory threshold of the restrained mice was found at SAR levels between 2 W kg(-1) and 5 W kg(-1). The breakdown of regulation was determined at 10.1 +/- 4.0 W kg(-1) for B6C3F1 mice and 7.7 +/- 1.6 W kg(-1) for NMRI mice. NMRI mice were more sensitive to thermal stress and responded at lower SAR values with regulation and breakdown.
Aitken RJ, Bennetts LE, Sawyer D, Wiklendt AM, King BV. · 2005
Researchers exposed mice to 900 MHz RFEMR at a specific absorption rate of approximately 90 mW/kg inside a waveguide for 7 days at 12 h per day. Sperm number, morphology, and vitality were not significantly affected by the exposure. However, detailed DNA analysis using QPCR revealed statistically significant damage to both the mitochondrial genome and the nuclear beta-globin locus.
Wolf FI et al. · 2005
Researchers exposed HL-60 leukemia cells, Rat-1 fibroblasts, and WI-38 diploid fibroblasts to 0.5–1.0-mT 50-Hz extremely low frequency electromagnetic fields for 24–72 hours. The treatment produced a dose-dependent increase in cell proliferation, with about a 30% increase after 72 hours of exposure to 1.0 mT. A dose-dependent increase in DNA damage was observed in all cell lines, with two peaks occurring at 24 and 72 hours. Both effects were prevented by pretreatment with α-tocopherol, suggesting that redox reactions were involved.
Lai H, Singh NP · 2005
Researchers studied four groups of rats: one exposed to 2450-MHz microwaves at 1 mW/cm2, one to magnetic field noise at 45 mG, one to both simultaneously, and a sham-exposed group. Brain cells of microwave-exposed rats had significantly higher levels of DNA single- and double-strand breaks compared with sham-exposed animals. Noise exposure alone did not significantly affect DNA strand break levels, but simultaneous noise exposure blocked the microwave-induced increases.
