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935 MHz cellular phone radiation. An in vitro study of genotoxicity in human lymphocytes.

机译:935 MHz手机辐射。人体淋巴细胞遗传毒性的体外研究。

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PURPOSE: The possibility of genotoxicity of radiofrequency radiation (RFR) applied alone or in combination with x-rays was investigated in vitro using several assays on human lymphocytes. The chosen specific absorption rate (SAR) values are near the upper limit of actual energy absorption in localized tissue when persons use some cellular telephones. The purpose of the combined exposures was to examine whether RFR might act epigenetically by reducing the fidelity of repair of DNA damage caused by a well-characterized and established mutagen. METHODS: Blood specimens from 14 donors were exposed continuously for 24 h to a Global System for Mobile Communications (GSM) basic 935 MHz signal. The signal was applied at two SAR; 1 and 2 W/Kg, alone or combined with a 1-min exposure to 1.0 Gy of 250 kVp x-rays given immediately before or after the RFR. The assays employed were the alkaline comet technique to detect DNA strand breakage, metaphase analyses to detect unstable chromosomal aberrations and sister chromatid exchanges, micronuclei in cytokinesis-blocked binucleate lymphocytes and the nuclear division index to detect alterations in the speed of in vitro cell cycling. RESULTS: By comparison with appropriate sham-exposed and control samples, no effect of RFR alone could be found for any of the assay endpoints. In addition RFR did not modify any measured effects of the x-radiation. CONCLUSIONS: This study has used several standard in vitro tests for chromosomal and DNA damage in Go human lymphocytes exposed in vitro to a combination of x-rays and RFR. It has comprehensively examined whether a 24-h continuous exposure to a 935 MHz GSM basic signal delivering SAR of 1 or 2 W/Kg is genotoxic per se or whether, it can influence the genotoxicity of the well-established clastogenic agent; x-radiation. Within the experimental parameters of the study in all instances no effect from the RFR signal was observed.
机译:目的:使用几种对人类淋巴细胞的测定方法,在体外研究了单独使用或与X射线结合使用的射频辐射(RFR)的遗传毒性的可能性。当人们使用某些蜂窝电话时,所选的特定吸收率(SAR)值接近于局部组织中实际能量吸收的上限。合并暴露的目的是检查RFR是否可以通过降低由特征明确的诱变剂引起的DNA损伤修复的保真度来表观遗传。方法:将来自14个供体的血液样本连续暴露于全球移动通信系统(GSM)基本935 MHz信号24小时。信号被施加在两个SAR; 1 W / Kg和2 W / Kg,单独或与RFR之前或之后在250 kVp X射线1.0 Gy中暴露1分钟有关。所采用的检测方法是碱性彗星技术,用于检测DNA链断裂;中期分析,用于检测不稳定的染色体畸变和姊妹染色单体交换;胞质分裂阻滞的双核淋巴细胞中的微核;核分裂指数用于检测体外细胞循环速度的变化。结果:通过与适当的假手术暴露和对照样品进行比较,没有发现单独的RFR可以用于任何测定终点。另外,RFR不会改变x射线的任何测量效果。结论:这项研究使用了几种标准的体外试验,以检测在体外暴露于X射线和RFR作用下的Go人淋巴细胞的染色体和DNA损伤。它已全面检查了连续1小时或2 W / Kg SAR的935 MHz GSM基本信号连续24小时暴露是否具有遗传毒性,或者它是否会影响成熟的成胶剂的遗传毒性; X射线。在所有情况下,在研究的实验参数范围内,均未观察到RFR信号的影响。

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