To investigate the frequency of micronuclei (as marker for genetic damage) in peripheral blood erythrocytes of mice that had been chronically exposed to radiofrequencies used for mobile communication.
1170 mice (585 males) were randomized into exposure groups, sham exposure groups and a cage control. Two frequencies (GSM/ 902 MHz and DCS/1747 MHz) were investigated and exposure level varied from low, medium to high. In all experimental conditions 50 animals of each sex were investigated for a two-year period and evaluation of micronuclei was performed after on survivors only. After the two years 6 sentinel mice (3 males) were used as positive control: they were injected with mitomycin C.
Exposure | Parameters |
---|---|
Exposure 1:
902 MHz
Exposure duration:
continuous for 2 h/day, 5 days/weeks for 2 years (see also add. information for exp. setup)
|
|
Exposure 2:
1,747 MHz
Exposure duration:
continuous for 2 h/day, 5 days/weeks for 2 years (see also add. information for exp. setup)
|
Frequency | 902 MHz |
---|---|
Type | |
Exposure duration | continuous for 2 h/day, 5 days/weeks for 2 years (see also add. information for exp. setup) |
Exposure source | |
---|---|
Setup | two parallel circular stainless steel plates placed 117 mm apart with a conical antenna in their center and stainless steel posts forming a cylindrical cavity of 755 mm radius, whre mice were placed in plastic tubes |
Sham exposure | A sham exposure was conducted. |
Additional info | 2 h daily exposure devided into three phases: phase 1: DTX mode simulating continuous talking phase 2: GSM talk simulating a conversation, i.e. temporal switching between DTX and non-DTX mode phase 3: GSM environment = non-DTX, DTX, power control, handovers according to their statistical occurrence during a conversation |
Measurand | Value | Type | Method | Mass | Remarks |
---|---|---|---|---|---|
SAR | 0.4 W/kg | maximum | - | whole body | low exposure group |
SAR | 1.3 W/kg | maximum | - | whole body | medium exposure group |
SAR | 4 W/kg | maximum | - | whole body | high exposure group |
SAR | 0.18 W/kg | peak value | - | partial body | low exposure group |
SAR | 1.9 W/kg | peak value | - | partial body | high exposure group |
Frequency | 1,747 MHz |
---|---|
Type | |
Exposure duration | continuous for 2 h/day, 5 days/weeks for 2 years (see also add. information for exp. setup) |
Exposure source | |
---|---|
Setup | two parallel circular stainless steel plates placed 117 mm apart with a bi-conical antenna in their center and stainless steel posts forming a cylindrical cavity of 755 mm radius, whre mice were placed in plastic tubes |
Sham exposure | A sham exposure was conducted. |
Additional info | 2 h daily exposure devided into three phases: phase 1: DTX mode simulating continuous talking phase 2: GSM talk simulating a conversation, i.e. temporal switching between DTX and non-DTX mode phase 3: GSM environment = non-DTX, DTX, power control, handovers according to their statistical occurrence during a conversation |
Measurand | Value | Type | Method | Mass | Remarks |
---|---|---|---|---|---|
SAR | 0.4 W/kg | maximum | - | whole body | low exposure group |
SAR | 1.3 W/kg | maximum | - | whole body | medium exposure group |
SAR | 4 W/kg | maximum | - | whole body | high exposure group |
SAR | 0.14 W/kg | peak value | - | partial body | low exposure group |
SAR | 3.3 W/kg | peak value | - | partial body | high exposure group |
The average number of survivors analyzed per treatment group was 39. There were no significant differences in the frequency of micronuclei between radiofrequency-exposed, sham-exposed, and cage control mice, irrespective of the staining/counting method used. Micronuclei were significantly increased in polychromatic and normochromatic erythrocytes of the positive control mice.
The data did not indicate radiofrequency-induced genotoxicity in mice after two years of exposure.
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