Dept. of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Institute for Electromagnetic Sensing of the Environment (IREA) - National Research Council (CNR), Naples, Italy.
Sci Rep. 2018 Sep 5;8(1):13234. doi: 10.1038/s41598-018-31636-7.
This study aims to assess whether a 1950 MHz radiofrequency (RF) electromagnetic field could protect human neuroblastoma SH-SY5Y cells against a subsequent treatment with menadione, a chemical agent inducing DNA damage via reactive oxygen species formation. Cells were pre-exposed for 20 h to specific absorption rate of either 0.3 or 1.25 W/kg, and 3 h after the end of the exposure, they were treated with 10 µM menadione (MD) for 1 h. No differences were observed between sham- and RF-exposed samples. A statistically significant reduction in menadione-induced DNA damage was detected in cells pre-exposed to either 0.3 or 1.25 W/kg (P < 0.05). Moreover, our analyses of gene expression revealed that the pre-exposure to RF almost inhibited the dramatic loss of glutathione peroxidase-based antioxidant scavenging efficiency that was induced by MD, and in parallel strongly enhanced the gene expression of catalase-based antioxidant protection. In addition, RF abolished the MD-dependent down-regulation of oxoguanine DNA glycosylase, which is a critical DNA repairing enzyme. Overall, our findings suggested that RF pre-exposure reduced menadione-dependent DNA oxidative damage, most probably by enhancing antioxidant scavenging efficiency and restoring DNA repair capability. Our results provided some insights into the molecular mechanisms underlying the RF-induced adaptive response in human neuroblastoma cells challenged with menadione.
这项研究旨在评估 1950MHz 射频(RF)电磁场是否可以保护人神经母细胞瘤 SH-SY5Y 细胞免受随后使用 menadione(一种通过活性氧形成诱导 DNA 损伤的化学试剂)的处理。细胞在暴露前 20 小时接受特定吸收率为 0.3 或 1.25 W/kg 的照射,暴露结束后 3 小时,用 10µM menadione(MD)处理 1 小时。假照和 RF 暴露样品之间没有差异。在预暴露于 0.3 或 1.25 W/kg 的细胞中,menadione 诱导的 DNA 损伤明显减少(P<0.05)。此外,我们的基因表达分析表明,RF 预暴露几乎抑制了 MD 诱导的谷胱甘肽过氧化物酶抗氧化清除效率的剧烈丧失,并平行地强烈增强了基于过氧化氢酶的抗氧化保护的基因表达。此外,RF 消除了 MD 依赖性的鸟嘌呤 DNA 糖基化酶的下调,该酶是一种关键的 DNA 修复酶。总的来说,我们的发现表明,RF 预暴露降低了 menadione 依赖性的 DNA 氧化损伤,这可能是通过增强抗氧化清除效率和恢复 DNA 修复能力来实现的。我们的结果为 RF 诱导的人神经母细胞瘤细胞对 menadione 挑战的适应性反应的分子机制提供了一些见解。
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