To study the effect of weak 8.15-18 GHz microwaves on the tumor necrosis factor secretion and the T lymphocytes proliferative response.
Exposure | Parameters |
---|---|
Exposure 1:
10 GHz
Modulation type:
CW
Exposure duration:
continuous for 0.5 h to 7 days
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|
Exposure 2:
8.15–18 GHz
Exposure duration:
continuous for 0.5 h to 7 days
|
|
A total of 45 and 60 animals were exposed in E1 and E2, respectively. The same numbers of animals were used for cage control. In both experiments, 10 animals were sham irradiated and 10 were untreated. The procedure was double blind.
Frequency | 10 GHz |
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Type | |
Waveform | |
Exposure duration | continuous for 0.5 h to 7 days |
Modulation type | CW |
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Exposure source |
|
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Distance between exposed object and exposure source | 80 cm |
Setup | Groups of five unrestrained mice were exposed in plastic cages (25 cm x 25 cm x 45 cm) without roof. There was no reflecting material on the floor beneath the animals. |
Sham exposure | A sham exposure was conducted. |
Additional info | Unexposed cage control animals were housed in a separate room under the same conditions. |
Measurand | Value | Type | Method | Mass | Remarks |
---|---|---|---|---|---|
power density | 1 µW/cm² | spatial average | measured | - | 0.2-1.6 µW/cm² |
SAR | 5 mW/kg | - | estimated | - | 2-5 mW/kg |
Frequency | 8.15–18 GHz |
---|---|
Type | |
Waveform | |
Exposure duration | continuous for 0.5 h to 7 days |
Exposure source |
|
---|---|
Sham exposure | A sham exposure was conducted. |
Measurand | Value | Type | Method | Mass | Remarks |
---|---|---|---|---|---|
power density | 1 µW/cm² | spatial average | measured | - | 0.2-1.6 µW/cm² |
SAR | 5 mW/kg | - | estimated | - | 2-5 mW/kg |
Whole body microwave irradiation caused a significant enhancement of tumor necrosis factor production in peritoneal macrophages and splenic T lymphocytes. Microwave exposure affected T cells, facilitating their capacity to proliferate in response to mitogenic stimulation. The irradiation duration necessary for the stimulation of cellular immunity ranged from 5 h to 3 days.
Chronic exposure for 7 days produced the decreasing of tumor necrosis factor production in macrophages.
The irradiation of the animals for 24 h increased the tumor necrosis factor production and immune proliferative response, and these stimulatory effects persisted over 3 days after the termination of exposure.
Microwave treatment increased the endogenously produced tumor necrosis factor more effectively than did lipopolysaccharide (one of the most potential stimuli of synthesis of this cytokine).
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