To study whether endogenous opioids are involved in radiofrequency irradiation-induced DNA double-strand breaks.
Rats were treated with the opioid antagonist naltrexone immediately before and after exposure.
Exposure | Parameters |
---|---|
Exposure 1:
2.45 GHz
Modulation type:
pulsed
Exposure duration:
continuous for 2 h
|
|
There were four treatment groups: RFR/naltrexone, sham/naltrexone, RFR/vehicle and sham vehicle.
Frequency | 2.45 GHz |
---|---|
Charakteristic |
|
Exposure duration | continuous for 2 h |
Modulation type | pulsed |
---|---|
Pulse width | 2 µs |
Packets per second | 500 |
Measurand | Value | Type | Method | Mass | Remarks |
---|---|---|---|---|---|
power density | 20 W/m² | mean | - | - | - |
SAR | 1.2 mW/g | mean | unspecified | whole body | - |
Data showed that the radiofrequency exposure significantly increased DNA double-strand breaks in brain cells of the rat. The effect was partially blocked by treatment with naltrexone. Thus, the results indicate that endogenous opioids play mediating role in radiofrequency exposure-induced DNA double-strand breaks in rat brain cells.
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