この研究は、ゲノム損傷の現れとしての有糸分裂擾乱の結果生じる可能性がある小核の誘導を指標に、900MHzの携帯電話電磁界の影響を、ヒト細胞としてHaCat細胞、ヒト‐ハムスター・ハイブリッド細胞としてA(L)細胞の2種類の細胞を用いて調べた。ばく露後の異なるインキュベーション期間の後、細胞を固定し、小核の発生頻度を評価した結果、どちらの種類の細胞にもばく露によるゲノム損傷は見られなかったと報告している。
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To study the potential of radiofrequency electromagnetic fields (900 MHz) to cause a genomic damage in the form of micronucleus induction.
After different post-exposure incubation periods (4 h or 22 h, with or without cytochalasin B), cells were fixed and micronucleus frequencies were evaluated. Cells treated with methyl methanesulfonate for 4 h were used as positive control.
ばく露 | パラメータ |
---|---|
ばく露1:
900 MHz
Modulation type:
CW
ばく露時間:
continuous for 30 min (both cell types) or 22 h (AL cells only)
both cell types
|
|
ばく露2:
900 MHz
Modulation type:
pulsed
ばく露時間:
continuous for 30 min
AL cells only
|
|
周波数 | 900 MHz |
---|---|
タイプ |
|
特性 |
|
ばく露時間 | continuous for 30 min (both cell types) or 22 h (AL cells only) |
Additional information | both cell types |
Modulation type | CW |
---|
ばく露の発生源/構造 |
|
---|---|
ばく露装置の詳細 | cells placed in slide flasks positioned in the center of the µTEM cell; a µTEM cell is a widened coaxial waveguide in which the inner conductor transforms from a round wire at the input and output ports to a thin plate in the center; above and beneath this plate the field is homogeneous; slide flasks at the bottom of the housing underneath the plate; µTEM cell temperature-regulated with a Peltier element and placed inside a thermally isolating styrofoam box; µTEM cell terminated with a 50 Ω resistor to ensure travelling wave conditions |
Sham exposure | A sham exposure was conducted. |
測定量 | 値 | 種別 | Method | Mass | 備考 |
---|---|---|---|---|---|
電界強度 | 90 V/m | effective value | 計算値 | - | 5, 10, 30, 90 V/m |
周波数 | 900 MHz |
---|---|
タイプ |
|
特性 |
|
ばく露時間 | continuous for 30 min |
Additional information | AL cells only |
ばく露の発生源/構造 |
|
---|---|
Sham exposure | A sham exposure was conducted. |
測定量 | 値 | 種別 | Method | Mass | 備考 |
---|---|---|---|---|---|
電界強度 | 90 V/m | effective value | 計算値 | - | 5, 10, 30, 90 V/m |
Both cell types did not show any genomic damage after exposure. To adapt the protocol for the micronucleus test into the direction of the protocol for mitotic disturbances, the post-exposure incubation period was reduced (4 h). and exposure time was extended to one cell cycle length (22 h). This did not result in any increase of the genomic damage.
In conclusion, micronucleus induction was not observed as a consequence of exposure to non-ionizing radiation, even though this agent was reported to cause mitotic disturbances under similar experimental conditions (see Schmid and Schrader 2007, Schrader et al. 2008, Schrader et al. 2011).
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