DNA Damage and Genotoxicity
polychromatic erythrocytes micronucleus frequency in the peripheral blood was
increased on day 8.
Zotti-Martelli et al.  exposed human peripheral blood lymphocytes in G(0) phase
to electromagnetic fields at different frequencies (2.45 and 7.7 GHz) and power
densities (10, 20 and 30 mW/cm2) for 15, 30 or 60min. The results showed for both
radiation frequencies an induction of micronuclei as compared to control cultures at a
power density of 30mW/cm2 and after an exposure of 30 and 60 min.
Zotti-Martelli et al.  exposed whole blood samples from nine different healthy
donors for 60, 120 and 180 min to continuous-wave 1800-MHz microwaves at power
densities of 5, 10 and 20 mW/cm2. A statistically significant increase of micronucleus
in lymphocytes was observed dependent on exposure time and power density. A
considerable decrease in spontaneous and induced MN frequencies was measured in a
III B. Micronucleus studies that reported no significant effects:
Bisht et al.  exposed C3H 10T½ cells to 847.74 MHz CDMA (3.2 or 4.8 W/kg) or
835.62 MHz FDMA (3.2 or 5.1 W/kg) RFR for 3, 8, 16 or 24 h. No exposure
condition was found to result in a significant increase relative to sham-exposed cells
either in the percentage of binucleated cells with micronuclei or in the number of
micronuclei per 100 binucleated cells.
Juutilainen et al.  found no significant change in micronucleus frequency in
erythrocytes of mice after long-term exposure to various mobile phone frequencies.
Koyama et al.  exposed Chinese hamster ovary (CHO)-K1 cells to 2450-MHz
microwaves for 2 h at average specific absorption rates (SARs) of 5, 10, 20, 50, 100,
and 200 W/kg. Micronucleus frequency in cells exposed at SARs of 100 and 200
W/kg were significantly higher when compared with sham-exposed controls. They
speculated that the effect observed was a thermal effect.
Port et al.  reported that exposure of HL-60 cells to EMFs 25 times higher than the
ICNIRP reference levels for occupational exposure did not induce any significant
changes in apoptosis, micronucleation, abnormal morphologies and gene expression.
Scarfi et al  exposed human peripheral blood lymphocytes to 900 MHz GSM
signal at specific absorption rates of 0, 1, 5 and 10 W/kg peak values. No significant
change in micronucleus frequency was observed.
Vijayalaximi et al. [1997a] exposed human blood to continuous-wave 2450- MHz
microwaves, either continuously for a period of 90 min or intermittently for a total
exposure period of 90 min (30 min on and 30 min off, repeated three times). The
mean power density at the position of the cells was 5.0 mW/cm2 and mean specific
absorption rate was 12.46 W/kg. There were no significant differences between RFRexposed and sham-exposed lymphocytes with respect to; (a) mitotic indices; (b)
incidence of cells showing chromosome damage; (c) exchange aberrations; (d)
acentric fragments; (e) binucleate lymphocytes, and (f) micronuclei.
Vijayalaximi et al. [1997b] exposed C3H/HeJ mice for 20 h/day, 7 days/week, over 18
months to continuous-wave 2450 MHz microwaves at a whole-body average specific
absorption rate of 1.0 W/kg. At the end of the 18 months, peripheral blood and bone
marrow smears were examined for the extent of genotoxicity as indicated by the