この研究は、ラットを対象に、パルス変調マイクロ波(2450MHz、1mW / cm2、平均全身SAR 0.6W / kg、パルス幅2マイクロ秒、500pps)の単回ばく露(45分間)および反復ばく露(1日45分間、毎日、10日間)が大脳皮質、海馬、および小脳のベンゾジアゼピン受容体の濃度および親和性に与える影響を調べた。リガンドとして3 H-フルニトラゼパムを用いた受容体結合アッセイを使用した。その結果、単回ばく露では、ばくろ直後に、大脳皮質での受容体濃度の上昇が認められたが、海馬や小脳には顕著な影響は見られなかった;調べたどの脳領域においても、受容体の結合親和性に有意な変化は観察されなかった;反復ばく露では、最後のばく露直後において、大脳皮質での受容体濃度の有意な変化は見られず、これは反復ばく露に対する適応である可能性がある、と報告している。
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To study the effects of single (45 min) and repeated (ten daily 45-min sessions) microwave exposures on the concentration and affinity of benzodiazepine receptors in the hippocampus, cerebellum, and cerebral cortex of the rat.
The benzodiazepine receptors coupled to GABA receptors and chloride channels play a significant role in mediating stress and anxiety responses in animals. In addition, a separate experiment was done to investigate whether factors in the irradiation environment contribute to the effect of microwaves on benzodiazepine receptors: Rats were adapted to the exposure environment before exposure to microwaves. The animals were placed in waveguides, given food and water, and after 24 h were subjected to microwave or sham irradiation for 45 min.
周波数 | 2.45 GHz |
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タイプ |
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偏波 |
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ばく露時間 | continuous for 45 min |
Modulation type | pulsed |
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Pulse width | 2 µs |
Packets per second | 500 |
ばく露の発生源/構造 |
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ばく露装置の詳細 | cylindrical Plexiglas chamber with a diameter of 15 cm, 24 cm long inside the waveguide |
Sham exposure | A sham exposure was conducted. |
周波数 | 2.45 GHz |
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タイプ |
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偏波 |
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ばく露時間 | 45 min/day for 10 days |
Modulation type | pulsed |
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Pulse width | 2 µs |
Packets per second | 500 |
ばく露の発生源/構造 |
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Sham exposure | A sham exposure was conducted. |
After a single exposure, an increase in the concentration of receptor was observed in the cerebral cortex, but no significant effect was observed in the hippocampus or cerebellum. No significant change in binding affinity of the receptors was observed in any of the brain regions investigated. In animals subjected to repeated exposures, no significant change in receptor concentration was found in the cerebral cortex immediately after the last exposure, which may indicate an adaptation to repeated exposures. The results also show that handling and exposure procedures in the experiments did not significantly affect benzodiazepine receptors. Because benzodiazepine receptors in the brain are responsive to anxiety and stress, the data support the hypothesis that low-intensity microwave exposure can be a source of stress.
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