Kerbacher J J, Meltz M L, Erwin D N
University of Texas Health Science Center, San Antonio 78284.
Radiat Res. 1990 Sep;123(3):311-9.
A limited number of contradictory reports have appeared in the literature about the ability of radiofrequency (rf) radiation to induce chromosome aberrations in different biological systems. The technical documentation associated with such reports is often absent or deficient. In addition, no information is available as to whether any additional genotoxic hazard would result from a simultaneous exposure of mammalian cells to rf radiation and a chemical which (by itself) induces chromosome aberrations. In the work described, we have therefore tested two hypotheses. The first is that rf radiation by itself, at power densities and exposure conditions which are higher than is consistent with accepted safety guidelines, can induce chromosome aberrations in mammalian cells. The second is that, during a simultaneous exposure to a chemical known to be genotoxic, rf radiation can affect molecules, biochemical processes, or cellular organelles, and thus result in an increase or decrease in chromosome aberrations. Mitomycin C (MMC) and Adriamycin (ADR) were selected because they act by different mechanisms, and because they might put normal cells at risk during combined-modality rf radiation (hyperthermia)-chemotherapy treatment of cancer. The studies were performed with suitable 37 degrees C and equivalent convection heating-temperature controls in a manner designed to discriminate between any thermal and possible nonthermal action. Radiofrequency exposures were conducted for 2 h under conditions resulting in measurable heating (a maximum increase of 3.2 degrees C), with pulsed-wave rf radiation at a frequency of 2450 MHz and an average net forward power of 600 W, resulting in an SAR of 33.8 W/kg. Treatments with MMC or ADR were for a total of 2.5 h and encompassed the 2-h rf radiation exposure period. The CHO cells from each of the conditions were subsequently analyzed for chromosome aberrations. In cells exposed to rf radiation alone, and where a maximum temperature of approximately 40 degrees C was achieved in the tissue culture medium, no alteration in the frequency from 37 degrees C control levels was observed. Relative to the chemical treatment with MMC alone at 37 degrees C, for two different concentrations, no alteration was observed in the extent of chromosome aberrations induced by either simultaneous rf radiation exposure or convection heating to equivalent temperatures. At the ADR concentration that was used, most of the indices of chromosome aberrations which were scored indicated a similar result.(ABSTRACT TRUNCATED AT 400 WORDS)
关于射频(rf)辐射在不同生物系统中诱导染色体畸变的能力,文献中出现了一些相互矛盾的报道。与这些报道相关的技术文档往往缺失或不足。此外,对于哺乳动物细胞同时暴露于射频辐射和一种(本身)能诱导染色体畸变的化学物质是否会产生任何额外的遗传毒性危害,尚无相关信息。因此,在所述工作中,我们检验了两个假设。第一个假设是,在高于公认安全准则的功率密度和暴露条件下,射频辐射本身可在哺乳动物细胞中诱导染色体畸变。第二个假设是,在同时暴露于一种已知具有遗传毒性的化学物质时,射频辐射可影响分子、生化过程或细胞器,从而导致染色体畸变增加或减少。选择丝裂霉素C(MMC)和阿霉素(ADR)是因为它们作用机制不同,且在癌症的联合射频辐射(热疗)-化疗治疗过程中可能使正常细胞处于危险之中。研究在合适的37℃以及等效对流加热温度对照下进行,其设计方式旨在区分任何热效应和可能的非热效应。在导致可测量加热(最大升温3.2℃)的条件下进行2小时的射频暴露,使用频率为2450MHz、平均净前向功率为600W的脉冲波射频辐射,比吸收率(SAR)为33.8W/kg。用MMC或ADR处理总共2.5小时,包括2小时的射频辐射暴露期。随后对每种条件下的中国仓鼠卵巢(CHO)细胞进行染色体畸变分析。在仅暴露于射频辐射且组织培养基中达到约40℃最高温度的细胞中,未观察到与37℃对照水平相比频率有变化。相对于在37℃单独用MMC进行化学处理,对于两种不同浓度,在同时进行射频辐射暴露或对流加热至等效温度时,所诱导的染色体畸变程度均未观察到变化。在所使用的ADR浓度下,所记录的大多数染色体畸变指标显示出类似结果。(摘要截取自400字)