この研究は、マウス海馬神経細胞由来HT22細胞において、アミロイドβ(Aβ)により誘発される細胞毒性に対し、無線周波電磁界ばく露(RF)を併用した場合の影響を調べた。まず、Aβ処置がHT22細胞増殖を濃度依存的に抑制することを確認した。一方、RFばく露は、細胞増殖に影響を与えず、またAβ誘発性の細胞増殖抑制に対してもほとんど影響しないことを確認した。さらにRF単独ばく露の場合、およびAβ処置とRFばく露を併用した場合について、細胞周期など詳細分析した結果、Aβにより誘発される細胞増殖抑制、ROS産生増加、細胞死の誘導に対し、RFばく露は有意な影響を与えなかったと報告している。
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The effects of exposure of mouse hippocampal neurons to combined 837 MHz and 1950 MHz electromagnetic fields on beta-amyloid protein-induced cytotoxicity should be investigated.
Few previous animal studies suggested beneficial effect of radiofrequency fields in Alzheimer's disease (Arendash et al. 2010, Banaceur et al. 2013). In contrast, EMF exposure was also found to increase beta-amyloid protein expression (Jiang et al. 2013). The present study should elucidate the possible mechanism of action in vitro.
Cells were divided into the following groups: 1) exposure to the electromagnetic fields only, 2) exposure to the electromagnetic fields and treatment with 5 µM beta-amyloid protein, 3) exposure to the electromagnetic fields and treatment with 50 µM beta-amyloid protein. For each group, a separate sham exposure group was used.
cells were treated with respective concentrations of beta-amyloid protein (5 µM and 50 µM) for 30 minutes prior to exposure to the electromagnetic fields
周波数 | 837–1,950 MHz |
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タイプ |
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ばく露時間 | continuous for 2 hours |
ばく露の発生源/構造 |
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Distance between exposed object and exposure source | 13.6 cm |
チャンバの詳細 | 100 mm petri dishes in exposure chamber with 37 ± 0.3°C and a 5% CO2 |
ばく露装置の詳細 | radial transmission line (RTL) exposure system with conical antenna, which was located in the center of the exposure chamber; petri dishes were placed at 13.6 cm from the antenna |
Sham exposure | A sham exposure was conducted. |
Exposure to the electromagnetic fields had no significant effect on any parameter in any group compared to the respective sham exposure groups.
The authors conclude that exposure of mouse hippocampal neurons to combined 837 MHz and 1950 MHz electromagnetic fields has no effects on the beta-amyloid protein-induced cytotoxicity.
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