この研究は、1800 MHzの高周波電磁界(RF- EMF)のばく露が、ヒトの血液細胞での活性酸素種(ROS)放出および/または熱ショックタンパク70(Hsp70)の発現変化を誘導するか否かを調べた。ROS放出への影響を調べる実験には、ヒト臍帯血由来の単球およびリンパ球を用い、1800 MHz の連続波または異なるGSM信号(GSM-DTXおよびGSM-Talk)を用いた。2 W / kgで、30または45分間の連続ばく露または断続ばく露(5 min ON/5 min OFF)をインキュベータ内で実施した。擬似ばく露およびホルボールエステルホルボール-12-ミリスチン酸-13-アセテート(PMA; 11μM)へのばく露(陽性対照)を実施した。Hsp70発現への影響を調べる実験には、ヒト単球を用い、2 W / kgのGSM-DTX信号に45分間ばく露を用い、陽性対照には熱処理(42°C)を用いた。ROS産生およびHsp70発現はフローサイトメトリ分析により測定した。擬似ばく露群および/または対照群との比較にはスチューデントのt検定を用いた。その結果、擬似ばく露群または対照群に比べ、PMA処理群では、ヒト単球およびリンパ球のROS産生が有意に増加した;ヒト単球で、連続的または断続的なGSM-DTX信号ばく露(2 W / kg)の後、擬似ばく露群に比べ、有意に異なるROS産生が検出された;しかし、この有意な差は、擬似ばく露群でのROS産生が低いために現れた;ヒトのリンパ球では、擬似ばく露群または対照群との差は検出されなかった;GSM-DTX信号ばく露終了から0、1、および2時間後のHsp70発現レベルに擬似ばく露群または対照群との差は検出されなかった、と報告している。
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To study if 1800 MHz radiofrequency electromagnetic fields can induce reactive oxygen species release and/or changes in heat shock protein 70 expression (to determine a possible inhibitor effect on free radical release) in human blood cells.
Human umbilical cord blood-derived monocytes and lymphocytes were used to examine reactive oxygen species release (cell stimulation with the phorbol ester tetradecanoylphorbol acetate (TPA) was used as positive control). To study HSP70 expression human monocytes were exposed (heat treatment at 42°C was used as positive control).
The cells were exposed to CW or different GSM signals (GSM-DTX, GSM-Talk), as described previously [Lantow et al., 2006].
Modulation type | CW |
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ばく露の発生源/構造 | |
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チャンバの詳細 | Two single-mode resonator cavities were placed within an incubator at 37°C (except heat-treatment) in a humidified atmosphere of 5% CO2 in air. Exposure and sham conditions were blindly and randomly assigned to the two waveguides by the computer-controlled signal unit [Schuderer et al., 2004]. |
ばく露装置の詳細 | Six 35 mm Petri dishes were placed in each waveguide on a dish holder, and in the H-field maxima of the standing waves inside the cavity. The temperature difference between sham and RF exposed cultures was not greater than 0.3°C. |
Sham exposure | A sham exposure was conducted. |
Additional information | The cells were exposed in parallel and in the same incubator to the following conditions: (1) non-treated (incubator control), (2) sham exposed, (3) RF-EMF exposed, (4) sham exposed + 1 µM PMA, (5) co-exposed to RF-EMF + PMA, (6) heat exposed at 42°C for 1 h. |
測定量 | 値 | 種別 | Method | Mass | 備考 |
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SAR | 2 W/kg | - | 測定値および計算値 | - | - |
ばく露の発生源/構造 |
|
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Sham exposure | A sham exposure was conducted. |
測定量 | 値 | 種別 | Method | Mass | 備考 |
---|---|---|---|---|---|
SAR | 2 W/kg | - | 測定値および計算値 | - | - |
Modulation type | pulsed |
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Repetition frequency | 217 Hz |
Additional information |
GSM-Talk (34% speaking and 66% hearing): temporal changes between 11 s non-DTX and 6 s DTX (average durations); crest factor of 11.9. |
ばく露の発生源/構造 |
|
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Sham exposure | A sham exposure was conducted. |
測定量 | 値 | 種別 | Method | Mass | 備考 |
---|---|---|---|---|---|
SAR | 2 W/kg | - | 測定値および計算値 | - | - |
The TPA treatment induced a significant increase in reactive oxygen species production in monocytes and lymphocytes compared to sham-exposed or to incubator controls. After continuous or intermittent GSM-DTX signal exposure (2 W/kg), a significantly different reactive oxygen species production was detected in monocytes compared to sham-exposed cells. However, this significant difference appeared due to the lowered value of reactive oxygen species during sham exposure. In lymphocytes, no differences could be revealed if data were compared either to sham-exposed or to incubator control.
The HSP70 expression level after 0, 1, and 2 h post-exposure to GSM-DTX signal at 2 W/kg for 1 h did not show any differences compared to the incubator or to sham-exposed control.
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