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首页> 外文期刊>Bioelectromagnetics. >Evaluation of genotoxic effects in human leukocytes after in vitro exposure to 1950 MHz UMTS radiofrequency field.
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Evaluation of genotoxic effects in human leukocytes after in vitro exposure to 1950 MHz UMTS radiofrequency field.

机译:体外暴露于1950 MHz UMTS射频场后对人白细胞的遗传毒性作用的评估。

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In the present study the third generation wireless technology of the Universal Mobile Telecommunication System (UMTS) signal was investigated for the induction of genotoxic effects in human leukocytes. Peripheral blood from six healthy donors was used and, for each donor, intermittent exposures (6 min RF on, 2 h RF off) at the frequency of 1950 MHz were conducted at a specific absorption rate of 2.2 W/kg. The exposures were performed in a transverse electro magnetic (TEM) cell hosted in an incubator under strictly controlled conditions of temperature and dosimetry. Following long duration intermittent RF exposures (from 24 to 68 h) in different stages of the cell cycle, micronucleus formation was evaluated by applying the cytokinesis block micronucleus assay, which also provides information on cell division kinetics. Primary DNA damage (strand breaks/alkali labile sites) was also investigated following 24 h of intermittent RF exposures, by applying the alkaline single cell gel electrophoresis (SCG)/comet assay. Positive controls were included by treating cell cultures with Mitomycin-C and methylmethanesulfonate for micronucleus and comet assays, respectively. The results obtained indicate that intermittent exposures of human lymphocytes in different stages of cell cycle do not induce either an increase in micronucleated cells, or change in cell cycle kinetics; moreover, 24 h intermittent exposures also fail to affect DNA structure of human leukocytes soon after the exposures, likely indicating that repairable DNA damage was not induced.
机译:在本研究中,研究了通用移动电信系统(UMTS)信号的第三代无线技术在人白细胞中的遗传毒性作用。使用来自六位健康供体的外周血,并且对于每位供体,以2.2 W / kg的特定吸收率进行1950 MHz频率的间歇暴露(RF开启6分钟,RF关闭2小时)。在严格控制的温度和剂量测定条件下,在培养箱中的横向电磁(TEM)单元中进行曝光。在细胞周期的不同阶段进行长时间的间歇性RF暴露(24至68小时)后,通过胞质分裂阻滞微核试验评估了微核的形成,该试验还提供了有关细胞分裂动力学的信息。通过应用碱性单细胞凝胶电泳(SCG)/彗星测定法,对间歇性RF暴露24小时后的原发性DNA损伤(链断裂/碱不稳定位点)进行了研究。通过分别用丝裂霉素-C和甲磺酸甲酯处理细胞培养物分别用于微核和彗星试验来包括阳性对照。获得的结果表明,人淋巴细胞在细胞周期不同阶段的间歇性暴露不会诱导微核细胞的增加或细胞周期动力学的改变。此外,24 h间歇性暴露也不能在暴露后立即影响人白细胞的DNA结构,这可能表明未诱导可修复的DNA损伤。

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