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受甲萘醌挑战的人神经母细胞瘤细胞中 1950MHz 电磁场的保护作用。

Protective effect of 1950 MHz electromagnetic field in human neuroblastoma cells challenged with menadione.

机构信息

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.

出版信息

Sci Rep. 2018 Sep 5;8(1):13234. doi: 10.1038/s41598-018-31636-7.


DOI:10.1038/s41598-018-31636-7
PMID:30185877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6125585/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/39a831b6ade9/41598_2018_31636_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/9117b318c0af/41598_2018_31636_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/85f1d533002b/41598_2018_31636_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/0d50c19df341/41598_2018_31636_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/9d966a6f837d/41598_2018_31636_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/39a831b6ade9/41598_2018_31636_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/9117b318c0af/41598_2018_31636_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/85f1d533002b/41598_2018_31636_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/0d50c19df341/41598_2018_31636_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/9d966a6f837d/41598_2018_31636_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8e/6125585/39a831b6ade9/41598_2018_31636_Fig5_HTML.jpg

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[3]
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[4]
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[5]
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[7]
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[8]
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本文引用的文献

[1]
Power frequency magnetic field promotes a more malignant phenotype in neuroblastoma cells via redox-related mechanisms.

Sci Rep. 2017-9-13

[2]
Adaptive response in mouse bone marrow stromal cells exposed to 900MHz radiofrequency fields: Impact of poly (ADP-ribose) polymerase (PARP).

Mutat Res Genet Toxicol Environ Mutagen. 2017-8

[3]
Adaptive Response Induced by Pre-Exposure to 915 MHz Radiofrequency: A Possible Role for Antioxidant Enzyme Activity.

J Biomed Phys Eng. 2017-6-1

[4]
Redox regulation of mitochondrial functional activity by quinones.

Physiol Int. 2016-12

[5]
Redox dynamics of manganese as a mitochondrial life-death switch.

Biochem Biophys Res Commun. 2017-1-15

[6]
Regular and Moderate Exercise Counteracts the Decline of Antioxidant Protection but Not Methylglyoxal-Dependent Glycative Burden in the Ovary of Reproductively Aging Mice.

Oxid Med Cell Longev. 2016

[7]
Adverse and beneficial effects in Chinese hamster lung fibroblast cells following radiofrequency exposure.

Bioelectromagnetics. 2017-5

[8]
ROS homeostasis and metabolism: a dangerous liason in cancer cells.

Cell Death Dis. 2016-6-9

[9]
Adaptive response in mouse bone-marrow stromal cells exposed to 900-MHz radiofrequency fields: Gamma-radiation-induced DNA strand breaks and repair.

J Toxicol Environ Health A. 2016

[10]
Improved Mitochondrial and Methylglyoxal-Related Metabolisms Support Hyperproliferation Induced by 50 Hz Magnetic Field in Neuroblastoma Cells.

J Cell Physiol. 2016-1-28

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