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3G手机的2100兆赫射频辐射与大脑中的DNA氧化损伤

The 2100MHz radiofrequency radiation of a 3G-mobile phone and the DNA oxidative damage in brain.

作者信息

Sahin Duygu, Ozgur Elcin, Guler Goknur, Tomruk Arın, Unlu Ilhan, Sepici-Dinçel Aylin, Seyhan Nesrin

机构信息

Department of Medical Biochemistry, Başkent University Faculty of Medicine, Ankara, Turkey.

Department of Biophysics, Gazi University Faculty of Medicine and Gazi Non-Ionizing Radiation Protection Center, Ankara, Turkey.

出版信息

J Chem Neuroanat. 2016 Sep;75(Pt B):94-8. doi: 10.1016/j.jchemneu.2016.01.002. Epub 2016 Jan 8.

Abstract

We aimed to evaluate the effect of 2100MHz radiofrequency radiation emitted by a generator, simulating a 3G-mobile phone on the brain of rats during 10 and 40 days of exposure. The female rats were randomly divided into four groups. Group I; exposed to 3G modulated 2100MHz RFR signal for 6h/day, 5 consecutive days/wk for 2 weeks, group II; control 10 days, were kept in an inactive exposure set-up for 6h/day, 5 consecutive days/wk for 2 weeks, group III; exposed to 3G modulated 2100MHz RFR signal for 6h/day, 5 consecutive days/wk for 8 weeks and group IV; control 40 days, were kept in an inactive exposure set-up for 6h/day, 5 consecutive days/wk for 8 weeks. After the genomic DNA content of brain was extracted, oxidative DNA damage (8-hydroxy-2'deoxyguanosine, pg/mL) and malondialdehyde (MDA, nmoL/g tissue) levels were determined. Our main finding was the increased oxidative DNA damage to brain after 10 days of exposure with the decreased oxidative DNA damage following 40 days of exposure compared to their control groups. Besides decreased lipid peroxidation end product, MDA, was observed after 40 days of exposure. The measured decreased quantities of damage during the 40 days of exposure could be the means of adapted and increased DNA repair mechanisms.

摘要

我们旨在评估一台模拟3G手机的发生器发出的2100MHz射频辐射在暴露10天和40天期间对大鼠大脑的影响。将雌性大鼠随机分为四组。第一组:每天暴露于3G调制的2100MHz射频辐射信号6小时,每周连续5天,共2周;第二组:先对照10天,然后在非活性暴露装置中每天放置6小时,每周连续5天,共2周;第三组:每天暴露于3G调制的2100MHz射频辐射信号6小时,每周连续5天,共8周;第四组:先对照40天,然后在非活性暴露装置中每天放置6小时,每周连续5天,共8周。提取大脑基因组DNA后,测定氧化DNA损伤(8-羟基-2'-脱氧鸟苷,pg/mL)和丙二醛(MDA,nmol/g组织)水平。我们的主要发现是,与对照组相比,暴露10天后大脑的氧化DNA损伤增加,而暴露40天后氧化DNA损伤减少。此外,暴露40天后观察到脂质过氧化终产物丙二醛减少。暴露40天期间测得的损伤量减少可能是适应性DNA修复机制增强的表现。

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