この研究は、発作を起こしやすい傾向を持つように作成された動物を用いて、脳活動に対する携帯電話様の電磁放射の影響を調べた。ピクロトキシンのけいれん閾値下用量の急性投与により発作傾向のある実験モデルに変換されたラットに、携帯電話と同様の強度で、2時間のGSM変調900 MHz電磁放射へのばく露を与えると、発作が誘発され、新皮質、古皮質、海馬、視床の神経活動マーカであるc-Fosのレベルが著しく上昇した。同様のピクロトキシン処理ラットでも無ばく露の場合は、発作を起こさず、脳のc-Fos数は有意に低かった。ピクロトキシンで前処理されていないラットにおいては、ばく露、無ばく露によってそのような差異は起こさなかった、と報告している。
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To study the effects of 2 h mobile phone irradiation (GSM) on rats made seizure-prone by injection of a subconvulsive dose of the GABA antagonist picrotoxin.
The effects were evaluated by observation of whether the rats suffered seizures and post mortem by immunochemical testing of relevant brain areas for c-Fos (a marker of neuronal activation that is produced in these brain areas by seizures).
4 groups of rats were invesigated (each of 7-8 rats): 1) Injection of picrotoxin (2 mg/kg) and exposure to irradiation, 2) injection of picrotoxin, 3) irradiation, 4) exposure to neither irradiation nor picrotoxin.
ばく露 | パラメータ |
---|---|
ばく露1:
900 MHz
Modulation type:
pulsed
ばく露時間:
continuous for 2 h
|
|
ばく露2:
900 MHz
Modulation type:
pulsed
ばく露時間:
continuous for 2 h
Picrotoxin-treated
|
Four groups of rats were given the following treatments: injection of picrotoxin, exposure to radiation, picrotoxin and radiation, neither picrotoxin nor radiation.
周波数 | 900 MHz |
---|---|
タイプ |
|
ばく露時間 | continuous for 2 h |
Modulation type | pulsed |
---|---|
Repetition frequency | 217 Hz |
Additional information |
GSM-modulated |
ばく露の発生源/構造 |
|
---|---|
チャンバの詳細 | Rats were individually immobilised in a tube and placed in a irradiation cage previously calibrated for measurement of the irradiation absorbed. |
ばく露装置の詳細 | The rat was located between a irradiating antenna and a receiving antenna with its head at an EMF maximum (as determined by FDTD calculations for the setup). |
周波数 | 900 MHz |
---|---|
タイプ |
|
ばく露時間 | continuous for 2 h |
Additional information | Picrotoxin-treated |
Modulation type | pulsed |
---|---|
Repetition frequency | 217 Hz |
Additional information |
GSM-modulated |
ばく露の発生源/構造 |
|
---|---|
Additional information | Picrotoxin was injected i.p. immediately before exposure. |
Data of group 1 (picrotoxin and irradiation) showed that rats suffered seizures and the levels of the neuronal activity marker c-Fos in neocortex, paleocortex, hippocampus and thalamus increased markedly. Non-irradiated picrotoxin-treated animals did not suffer seizures, and their cerebral c-Fos counts were significantly lower. Irradiation caused no such differences in rats that had not been pretreated with picrotoxin.
The authors conclude that GSM-type irradiation can induce seizures in rats following their facilitation by subconvulsive doses of picrotoxin, and that research should be pursued into the possibility that this kind of irradiation may similarly affect brain function in humans with epileptic disorders.
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