この研究は、麻酔処置されたラットに、平均電力密度60 mW / cm 2(平均比吸収率12 W / kg)の5.6 GHzの連続波の無線周波電磁放射(RFR)ばく露を実施した。結腸温度を38.5℃から39.5℃に上昇させるようばく露した場合、クロルプロマジンの急性投与により、ばく露中断時のベースライン体温への復帰は早まった;ばく露を38.5℃で開始し、致死温度に達するまで続けた場合、クロルプロマジン投与ラットは食塩水投与ラットよりも生存期間が有意に短くなった;以上から、クロルプロマジンは、39.5℃以下の結腸温度で体温調節効率を高め、致死的なRFRばく露に対する感受性を増強した;2.8 GHzを用いた先行研究と比較すると、クロルプロマジンの効果は、2.8 GHzおよび5.6 GHzで同様であった、と報告している。
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To determine if chlorpromazine affects the thermal responses, heart rate, blood pressure, and respiratory rate of anesthetized rats during exposure to 5.6 GHz radiofrequency irradiation (this frequency is characteristic of high-power stationary tracking radars for military applications and of naval ship radars).
Experiments were performed that resulted in two stages: 1) exposures were performed that resulted in colonic temperture increase from 38.5 to 39.5°C, and 2) radiofrequency irradiation was initiated at 38.5°C and continued until death body temperatures were attained.
ばく露 | パラメータ |
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ばく露1:
5.6 GHz
Modulation type:
CW
ばく露時間:
until temperature rise of 1°C
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ばく露2:
5.6 GHz
Modulation type:
CW
ばく露時間:
until lethal colonic temperature; 29.5 +/- 2.6 min without saline treatment; 36.9 +/- 2.2 min saline-treated
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周波数 | 5.6 GHz |
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タイプ |
|
特性 |
|
ばく露時間 | until temperature rise of 1°C |
Additional information | exposure started at a colonic temperature of 38.5°C; exposure was discontinued when the colonic temperature increased to 39.5°C and it was initiated again when the temperature returned to 38.5°C; this procedure was continued for 6 cycles (drugs were administered before the 4th cycle). |
Modulation type | CW |
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ばく露の発生源/構造 |
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ばく露装置の詳細 | long axis of animal parallel to the magnetic field |
周波数 | 5.6 GHz |
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タイプ |
|
特性 |
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ばく露時間 | until lethal colonic temperature; 29.5 +/- 2.6 min without saline treatment; 36.9 +/- 2.2 min saline-treated |
Modulation type | CW |
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ばく露の発生源/構造 |
|
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After acute administration of chlorpromazine, body temperature exhibited a faster return to baseline temperature when irradiation was discontinued. When irradiation was initiated at 38.5°C and continued until lethal temperatures resulted, chlorpromazine-treated rats exhibited significantly shorter survival times than saline-treated rats. Thus, although chlorpromazine enhanced thermoregulatory efficiency at colonic temperatures below 39.5°C, the drug produced increased susceptibility to terminal radiofrequency irradiation.
The present findings, when compared to previous studies of irradiation at 2.8 GHz (e.g. publication 4486), suggest that the effects of chlorpromazine on thermal responses to radiofrequency irradiation during intermittent and terminal exposure are similar at both 2.8 and 5.6 GHz.
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