この研究は、1週間あるいは6週間のばく露期間で、1日2時間、無線周波(RF)電磁界のばく露を受けたマウスの末梢血および骨髄の赤血球、ならびにケラチノサイトおよび脾臓リンパ球における小核誘導の変化を調べた。実験に用いた電磁界は、GSM900およびDCS1800ハンドセットからのばく露をシミュレートしたものであり、通話(GSM Basic)、リスニング(DTX)および環境中の移動(ハンドオーバー、出力制御)において生じる低周波振幅変調成分が含まれた。搬送周波数は、システムのアップリンク帯域の中心、つまりGSMの場合は902 MHz、DCSの場合は1747 MHzに設定した。一様な全身ばく露を与えるように、ばく露セットアップに固定された円筒管内にマウスを拘束した。スロット平均全身SARは、1週間ばく露実験においては33.2、11.0、3.7および0 mW / g、6週間ばく露実験においては24.9、8.3、2.8および0 mW / gに調整された。このようなばく露レベルは、遺伝毒性のエンドポイントに影響を与える可能性のある熱的影響を持たないことを事前テストで確認した上で決定された。大腿骨の骨髄細胞(1週間ばく露実験)、末梢血の赤血球(6週間ばく露実験)、尾根部ケラチノサイトおよび脾臓のリンパ球(両方の実験)をそれぞれ、動物から単離、染色して小核の分析を行なった。その結果、どちらのばく露期間でも、またどちらの周波数においても、動物に臨床学的な異常は検出されなかった;RF電磁界ばく露は赤血球の形成に影響を及ぼさなかった;1週間ばく露後の多色性赤血球の正常色性赤血球に対する比率は、擬似ばく露群と差がなかった;RF電磁界ばく露群の骨髄または末梢血の赤血球、ケラチン産生細胞、または脾臓リンパ球での小核の発生数は、擬似ばく露群のものに比べ上昇しなかった、と報告している。
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To study the possible induction of micronuclei in erythrocytes of the peripheral blood and bone marrow from the femur and in keratinocytes from the tail root and spleen lymphocytes of mice exposed to radiofrequency irradiation for 2 h per day over periods of 1 and 6 weeks, respectively.
In the one-week study, immature polychromatic erythrocytes from bone marrow were used; in the 6-week study, mature normochromatic erythrocytes from the peripheral blood were used.
In the one week study, a seperate group of mice were treated with cyclophosphamide (30 mg/kg) and used as positive control.
ばく露 | パラメータ |
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ばく露1:
902–1,747 MHz
Modulation type:
pulsed
ばく露時間:
repeated daily exposure, 2 h/day, for 5 days
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|
ばく露2:
902–1,747 MHz
Modulation type:
pulsed
ばく露時間:
repeated daily exposure, 2 h/day, 5 days/week, for 6 weeks
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|
Modulation type | pulsed |
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Additional information |
The exposure signal applied consisted of three phases, each lasting 40 min: GSM Basic, GSM Talk consisting of random changes between the non-DTX (2/3) and DTX (1/3) modes, and GSM "Environment" including GSM features such as non-DTX, DTX, power control, and handovers according to their statistical occurrence based on data presented in [Wiart et al., 2000]. |
ばく露の発生源/構造 | |
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チャンバの詳細 | Two exposure systems were used for the experiments: one for exposure with a 902 MHz GSM signal and one for exposure with a 1747 MHz DCS signal. The exposure systems were located in separate animal rooms. The exposure system consisted of a signal generation, control and monitoring unit and four identical cylindrically shaped exposure units (wheels), each enabling exposure of up to 65 animals. The exposure unit was an adaptation of the Ferris-wheel concept used in [Balzano et al., 2000]. |
ばく露装置の詳細 | Each wheel consisted of two parallel circular stainless steel metal plates with a distance of 11.7 cm that were connected around the edges by parallel metal bars functioning as a shortcut to make the setup structure resonant. Either a conical antenna (902 MHz) or a bi-conical antenna (1747 MHz) was placed in the centre between the plates. In the 902 MHz setups, high-permittivity plastic bricks were also inserted between neighbouring tubes to increase the electrical distance and therefore suppress distortion from neighbouring animals. Encased between the plates were 65 tapered cylindrical polycarbonate tubes (i.d. 40 mm) arranged radially around the antenna. Each wheel housed 20 animals; all other positions were filled with mouse dummies of the same weight consisting of a conical plastic tube filled with a liquid with the same dielectrical parameters as muscle tissue. |
Sham exposure | A sham exposure was conducted. |
Additional information | Each exposure unit was adjusted to a different exposure level, resulting in four dose levels (high, medium, low and sham). The exposure levels for the 1- and 6-week studies were determined in a pre-test to confirm that no thermal effects occurred. In the 6-week study, exposure levels were slightly reduced, so that the high dose level was close to but below the thermal threshold. In the 1-week study, a separate group of rats was treated orally with cyclophosphamide as positive control. |
測定量 | 値 | 種別 | Method | Mass | 備考 |
---|---|---|---|---|---|
SAR | 33.2 mW/g | average over mass | 測定値および計算値 | whole body | maximum slot average high dose exposure |
SAR | 4 mW/g | average over mass | 測定値および計算値 | whole body | average high dose exposure phase I (phase II: 2.8 mW/g and phase III: 1.04 mW/g) |
SAR | 11.1 mW/g | average over mass | 測定値および計算値 | whole body | maximum slot average medium dose exposure |
SAR | 1.33 mW/g | average over mass | 測定値および計算値 | whole body | average medium dose exposure phase I (phase II: 0.93 mW/g and phase III: 0.35 mW/g) |
SAR | 3.7 mW/g | average over mass | 測定値および計算値 | whole body | maximum slot average low dose exposure |
SAR | 0.44 mW/g | average over mass | 測定値および計算値 | whole body | average low dose exposure phase I (phase II: 0.31 mW/g and phase III: 0.114 mW/g) |
Modulation type | pulsed |
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Additional information |
same as E1 |
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 | 24.9 mW/g | average over mass | 測定値および計算値 | whole body | maximum slot average high dose exposure |
SAR | 3 mW/g | average over mass | 測定値および計算値 | whole body | average high dose exposure phase I (phase II: 2.1 mW/g and phase III: 0.78 mW/g) |
SAR | 8.2 mW/g | average over mass | 測定値および計算値 | whole body | maximum slot average medium dose exposure |
SAR | 1 mW/g | average over mass | 測定値および計算値 | whole body | average medium dose exposure phase I (phase II: 0.7 mW/g and phase III: 0.26 mW/g) |
SAR | 2.7 mW/g | average over mass | 測定値および計算値 | whole body | maximum slot average low dose exposure |
SAR | 0.33 mW/g | average over mass | 測定値および計算値 | whole body | average low dose exposure phase I (phase II: 0.23 mW/g and phase III: 0.086 mW/g) |
The radiofrequency field exposure had no influence on the formation of red blood cells. After 1 week of exposure, the ratio of polychromatic to normochromatic erythrocytes was unchanged in the exposed groups compared to the sham-exposed groups.
Furthermore, the radiofrequency field exposure did not induce an increase in the number of micronuclei in erythrocytes of the bone marrow or peripheral blood, in keratinocytes, or in spleen lymphocytes compared to the sham-exposed control.
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