Maskey D et al. · 2010
Researchers measured calbindin (CB) and calretinin (CR) expression in the hippocampus of mice after exposure to 835 MHz electromagnetic fields at various durations and absorption rates. Exposure conditions included 1 hour per day for 5 days at a specific absorption rate of 1.6 W/kg, 1 hour per day for 5 days at 4.0 W/kg, 5 hours per day for 1 day at 1.6 W/kg, 5 hours per day for 1 day at 4.0 W/kg, and daily exposure for 1 month at 1.6 W/kg. Exposure for 1 month produced almost complete loss of pyramidal cells in the CA1 area. Body weights did not change significantly across the exposure groups.
Xu S et al. · 2010
Researchers exposed primary cultured cortical neurons to pulsed radiofrequency electromagnetic fields at 1800 MHz modulated by 217 Hz at an average specific absorption rate of 2 W/kg. At 24 hours after exposure, researchers found a significant increase in levels of 8-hydroxyguanine, a common biomarker of DNA oxidative damage, in the mitochondria of neurons. The copy number of mitochondrial DNA and the levels of mitochondrial RNA transcripts showed an obvious reduction after RF exposure. Each of these mitochondrial DNA disturbances could be reversed by pretreatment with melatonin.
Guler G, Tomruk A, Ozgur E, Seyhan N. · 2010
Researchers investigated oxidative DNA damage and lipid peroxidation levels in the brain tissue of pregnant and non-pregnant New Zealand White rabbits and their newborns exposed to radiofrequency radiation. The rabbits were exposed to radiofrequency radiation at 1800 MHz GSM at 14 V/m for 15 minutes per day over 7 days. MDA and 8-OHdG levels in exposed pregnant and non-pregnant rabbits were significantly increased compared to controls, but no difference was found in the newborns.
Ziemann C et al. · 2009
Researchers exposed male and female B6C3F1 mice to GSM 902 MHz and DCS 1747 MHz signals for two years. The exposure regimen was 2 hours per day, 5 days per week, at whole-body averaged SARs of 0.4, 1.3, and 4.0 W/kg. Micronuclei were counted in peripheral blood erythrocytes stained with May-Grunwald-Giemsa or acridine orange. No significant differences in micronuclei frequency were observed between RF-exposed, sham-exposed, and cage control mice. Positive control mice injected with mitomycin C had significantly increased micronuclei, and the authors concluded that the data did not indicate RF-induced genotoxicity after two years.
Hansteen IL et al. · 2009
The aim was to test if exposure used in mobile phones and wireless network technologies would induce DNA damage in cultured human lymphocytes with and without a known clastogen. Lymphocytes from six donors were exposed to 2.3 GHz, 10 W/m(2) continuous waves, or 2.3 GHz, 10 W/m(2) pulsed waves (200 Hz pulse frequency, 50% duty cycle). Mitomycin C was added to half of the cultures. No statistically significant differences were observed between control and exposed cultures. A weak trend for more chromosomal damage with the interaction of pulsed fields with mitomycin C compared to a constant field was observed.
Sannino A et al. · 2009
Researchers exposed human dermal fibroblasts from a healthy donor and a Turner's syndrome donor to 900 MHz RF radiation for 24 hours using a GSM-like signal at 1 W/kg, and Turner's syndrome fibroblasts were also exposed for 1 hour. For RF exposure alone, DNA damage was assessed with the alkaline comet assay and the cytokinesis-block micronucleus assay. RF radiation alone caused no genotoxic or cytotoxic effects in either cell line. MX increased DNA migration in the comet assay, but RF exposure did not enhance this MX-induced DNA damage.
Finnie JW, Blumbergs PC, Cai Z, Manavis J · 2009
Researchers exposed mice to 900 MHz radiofrequency fields at a specific absorption rate of 4 W/kg for 60 minutes or for 5 days per week over 104 weeks. Control mice were sham-exposed or freely moving to account for restraint stress, and a positive control group received a clostridial toxin that upregulates aquaporin-4. No immunohistochemically detectable up-regulation of aquaporin-4 was observed in exposed mouse brains after either short or long exposure durations.
Mousavy SJ et al. · 2009
Researchers investigated the effect of mobile phone RF (910 MHz and 940 MHz) on the structure and function of HbA. Oxygen affinity was measured using sodium dithionite with a UV-vis spectrophotometer, and structural changes were studied by circular dichroism and fluorescence spectroscopy. The results indicated that mobile phone EMFs altered oxygen affinity and tertiary structure of HbA. Furthermore, the decrease of oxygen affinity of HbA corresponded to the EMFs intensity and time of exposure.
Atay T et al. · 2009
Researchers investigated the effects of electromagnetic waves from cellular phones operating at 900 to 1800 MHz on bone mineral density of the human iliac bone wings in 150 male volunteers. Participants were divided into two groups based on the iliac side exposed to electromagnetic waves (group 1) and the unexposed side (group 2). The mean daily phone carriage duration was 14.7 hours and the mean duration of phone use was 6.2 years. Dual-energy x-ray absorptiometry measurements showed slightly lower values on the exposed side but the difference was not statistically significant (P > 0.05), and values were not as low as in osteopenia or osteoporosis.
Anghileri LJ, Mayayo E, Domingo JL. · 2009
The study found a synergism between aluminum and radiofrequency that increased early mortality in lymphoma-bearing mice. This synergism was stronger with aluminum lactate than with aluminum citrate due to higher ionization at physiological pH. The dissociation of aluminum complexes appears to induce a remarkable acceleration of mortality and lymphoid-related hypertrophy of the spleen and liver at an early age. Calcium chloride overload had no effect when cellular calcium homeostasis was functional. The researchers measured organ hypertrophy using the organ-to-body-weight ratio and histopathological examination.
Mailankot M et al. · 2009
Researchers exposed male albino Wistar rats to RF-EMR from an active GSM mobile phone for one hour daily over 28 days. Exposed rats had significantly reduced sperm motility but no change in total sperm count. RF-EMR exposure also increased lipid peroxidation and decreased glutathione levels in the testis and epididymis. Facial temperature did not change significantly during exposure.
Agarwal A et al. · 2009
After liquefaction, neat semen samples were divided into two aliquots, with one exposed to cellular phone radiation in talk mode for 1 hour and the other serving as an unexposed control under identical conditions. Exposed samples showed a significant decrease in sperm motility and viability, an increase in ROS level, and a decrease in ROS-TAC score. Levels of total antioxidant capacity and DNA damage showed no significant differences between exposed and unexposed samples.
Zareen N, Khan MY, Ali Minhas L · 2009
Embryos exposed for 10 post-incubation days showed decreased retinal growth and mild epithelial pigmentation. Extending exposure to 15 post-incubation days reversed growth retardation to enhancement and shifted pigmentation from mild to intense. The authors concluded that mobile phone EMF causes derangement of chicken embryo retinal differentiation. Retinal thickness and epithelial pigmentation grades were statistically compared between control and experimental groups.
Vácha M, Puzová T, Kvícalová M · 2009
Researchers tested how weak radio frequency magnetic fields affect the American cockroach's ability to sense the geomagnetic field. A 1.2 MHz field disrupted this sense at intensities between 12 nT and 18 nT, while a 2.4 MHz field required between 18 nT and 44 nT. A 7 MHz field had no effect even at the highest tested intensity of 44 nT. The disruptive effect was strongest at the Larmor frequency of 1.2 MHz. The researchers measured the rise in locomotor activity induced by periodic changes in the geomagnetic North position by 60 degrees.
Zhijian C et al. · 2009
Researchers used the in vitro comet assay to determine whether 1.8-GHz radiofrequency radiation can influence DNA repair in human leukocytes exposed to X-rays. Leukocytes from four young healthy donors were intermittently exposed to RFR at a SAR of 2 W/kg for 24 hours with fields on for 5 minutes and off for 10 minutes, then irradiated with X-rays at doses of 0.25, 0.5, 1.0 and 2.0 Gy. DNA damage was measured at 0, 15, 45, 90, 150 and 240 minutes after X-rays using percent tail DNA, and repair speed was assessed via DNA repair percentage. The results showed individual differences in DNA repair speeds among the four donors. Intermittent RFR exposure did not directly induce DNA damage or show synergistic effects with X-rays.
Tkalec M et al. · 2009
Researchers exposed Allium cepa seeds for two hours to 400 and 900MHz fields at strengths of 10, 23, 41 and 120Vm(-1), and also tested a four-hour exposure and modulation at 23Vm(-1). Germination rate and root length did not change significantly under any exposure condition. At 900MHz, higher field strengths (41 and 120Vm(-1)) and modulated fields significantly increased the mitotic index, while all 900MHz exposures increased the percentage of mitotic abnormalities. At 400MHz, the mitotic index increased only after modulated exposure, and higher numbers of mitotic abnormalities were found after modulated exposure and after higher field strengths (41 and 120Vm(-1)). The chromosomal aberrations were mainly lagging chromosomes, vagrants, disturbed anaphases and chromosome stickiness.
Sannino A et al. · 2009
Lymphocytes were collected at 72 hours to measure micronuclei frequency in cytokinesis-blocked binucleated cells. Four donors exhibited a significant reduction in micronuclei after RF pre-exposure, indicating an adaptive response. One donor showed no significant difference in micronuclei between pre-exposed and unexposed cells, indicating a non-responder. The data indicated heterogeneity in the induction of an adaptive response between individuals exposed to RF radiation.
Brescia F et al. · 2009
Researchers measured reactive oxygen species (ROS) production in human lymphoblastoid cells exposed to a 1950 MHz UMTS signal at Specific Absorption Rates of 0.5 and 2.0 W/kg. Exposures ranged from short durations of 5 to 60 minutes up to 24 hours, and the study also tested RF radiation given before or at the same time as ferrous ions. RF exposure did not increase ROS formation or affect cell viability, and combining RF with ferrous ions did not produce more ROS than ferrous ions alone.
Sirav B, Seyhan N · 2009
Researchers investigated the effects of 900 and 1,800 MHz continuous-wave radio frequency radiation on blood-brain barrier permeability in rats. Twenty minutes of exposure at both frequencies increased blood-brain barrier permeability in male rats, while female rats showed no change. The researchers noted that the scientific evidence on radio frequency radiation safety or harm remains inconclusive.
Del Vecchio G et al. · 2009
Luukkonen J et al. · 2009
Researchers exposed human SH-SY5Y neuroblastoma cells to 872 MHz radiofrequency radiation at 5 W/kg for 1 hour, combined with menadione, a chemical that induces intracellular ROS production and DNA damage. Continuous-wave RF radiation increased DNA breakage compared to cells exposed only to menadione, and ROS levels were higher at 30 and 60 minutes after exposure ended. No effects of the GSM signal were seen on either ROS production or DNA damage.
Del Vecchio G et al. · 2009
Researchers studied the effects of radiofrequency electromagnetic field exposure on neuronal maturation using two in vitro models: murine SN56 cholinergic cells and rat primary cortical neurons. Cells were exposed at 1 W/kg at 900 MHz GSM modulated, and neurite emission, outgrowth, and branching were examined at multiple time points. RF-EMF exposure reduced the number of neurites in both cell systems, and this reduction correlated with increased expression of beta-thymosin mRNA.
De Iuliis GN, Newey RJ, King BV, Aitken RJ. · 2009
Researchers exposed purified human spermatozoa in vitro to radio-frequency electromagnetic radiation tuned to 1.8 GHz across a range of specific absorption rates from 0.4 W/kg to 27.5 W/kg. As the SAR increased, sperm motility and vitality were significantly reduced, while mitochondrial reactive oxygen species generation and DNA fragmentation were significantly elevated (P<0.001). The researchers also observed highly significant relationships between SAR, the oxidative DNA damage biomarker 8-OH-dG, and DNA fragmentation after exposure.
Valbonesi P et al. · 2008
Researchers used the human trophoblast cell line HTR-8/SVneo to evaluate HSP70 and HSC70 protein and gene expression and primary DNA damage after nonthermal exposure to pulse-modulated 1817 MHz GSM-217 Hz waves for one hour at a SAR of 2 W/kg. Heat shock significantly enhanced HSP70 expression but not HSC70 expression. Exposure to high-frequency EMFs did not change HSP70 or HSC70 protein or gene expression. Hydrogen peroxide caused a significant increase in DNA strand breaks, but EMF exposure did not. Overall, no evidence was found that the exposure induced a HSP70-mediated stress response or primary DNA damage.
Prisco MG et al. · 2008
