Fritze K, Wiessner C, Kuster N, Sommer C, Gass P, Hermann D M, Kiessling M, Hossmann K A
Max-Planck-Institute for Neurological Research, Department of Experimental Neurology, Cologne, Germany.
Neuroscience. 1997 Dec;81(3):627-39. doi: 10.1016/s0306-4522(97)00228-5.
The acute effect of global system for mobile communication (GSM) microwave exposure on the genomic response of the central nervous system was studied in rats by measuring changes in the messenger RNAs of hsp70, the transcription factor genes c-fos and c-jun and the glial structural gene GFAP using in situ hybridization histochemistry. Protein products of transcription factors, stress proteins and marker proteins of astroglial and microglial activation were assessed by immunocytochemistry. Cell proliferation was evaluated by bromodeoxyuridine incorporation. A special GSM radiofrequency test set, connected to a commercial cellular phone operating in the discontinuous transmission mode, was used to simulate GSM exposure. The study was conducted at time averaged and brain averaged specific absorption rates of 0.3 W/kg (GSM exposure), 1.5 W/kg (GSM exposure) and 7.5 W/kg (continuous wave exposure), respectively. Immediately after exposure, in situ hybridization revealed slight induction of hsp70 messenger RNA in the cerebellum and hippocampus after 7.5 W/kg exposure, but not at lower intensities. A slightly increased expression of c-fos messenger RNA was observed in the cerebellum, neocortex and piriform cortex of all groups subjected to immobilization, but no differences were found amongst different exposure conditions. C-jun and GFAP messenger RNAs did not increase in any of the experimental groups. 24 h after exposure, immunocytochemical analysis of FOS and JUN proteins (c-FOS, FOS B, c-JUN JUN B, JUN D), of HSP70 or of KROX-20 and -24 did not reveal any alterations. Seven days after exposure, neither increased cell proliferation nor altered expression of astroglial and microglial marker proteins were observed. In conclusion, acute high intensity microwave exposure of immobilized rats may induce some minor stress response but does not result in lasting adaptive or reactive changes of the brain.
通过使用原位杂交组织化学技术测量热休克蛋白70(hsp70)、转录因子基因c-fos和c-jun以及神经胶质结构基因胶质纤维酸性蛋白(GFAP)信使核糖核酸(mRNA)的变化,研究了全球移动通信系统(GSM)微波辐射对大鼠中枢神经系统基因组反应的急性影响。通过免疫细胞化学评估转录因子的蛋白质产物、应激蛋白以及星形胶质细胞和小胶质细胞激活的标记蛋白。通过溴脱氧尿苷掺入评估细胞增殖。使用连接到以不连续传输模式运行的商用手机的特殊GSM射频测试装置来模拟GSM辐射。该研究分别在时间平均和大脑平均比吸收率为0.3W/kg(GSM辐射)、1.5W/kg(GSM辐射)和7.5W/kg(连续波辐射)的条件下进行。暴露后立即进行的原位杂交显示,在7.5W/kg辐射后,小脑和海马体中hsp70信使核糖核酸有轻微诱导,但在较低强度下未出现。在所有接受固定的组的小脑中,观察到c-fos信使核糖核酸的表达略有增加,但在不同暴露条件之间未发现差异。在任何实验组中,c-jun和GFAP信使核糖核酸均未增加。暴露24小时后,对FOS和JUN蛋白(c-FOS、FOS B、c-JUN、JUN B、JUN D)、HSP70或KROX-20和-24进行免疫细胞化学分析,未发现任何改变。暴露7天后,未观察到细胞增殖增加或星形胶质细胞和小胶质细胞标记蛋白表达改变。总之,对固定大鼠进行急性高强度微波辐射可能会诱导一些轻微的应激反应,但不会导致大脑产生持久的适应性或反应性变化。