この研究は、ラットを用いた実験で、マイクロ波ばく露がラットの胸腺組織に与える影響(酸化ストレス、DNA断片化、アポトーシス、および増殖)を調べ、さらに、それらの影響を対するメラトニンの効果を評価した。ウィスターラットを4群(各n = 21)に分けた。すなわち、擬似ばく露+生理食塩水投与群、擬似ばく露+メラトニン投与群、マイクロ波ばく露群、マイクロ波ばく露+メラトニン投与群である。携帯電話を用いたマイクロ波ばく露を、1日4時間で、20、40および60日間継続した。メラトニン(2 mg / kg)または生食の腹腔内投与も毎日行った。ばく露開始から20、40および60日目に、各群から7匹ずつ取り出して屠殺し、胸腺を摘出した。その結果、マイクロ波ばく露群において、マロンジアルデヒドおよびカルボニル基含有量の有意な増加、ならびにカタラーゼの減少およびキサンチンオキシダーゼ活性の増加が見られた;メラトニンは、マロンジアルデヒドおよびカルボニル基の含有量の増加を防止し、カタラーゼとキサンチンオキシダーゼ活性への影響を逆転させた;マイクロ波ばく露群では、アルカリ性および酸性の両方のDNase活性の増加、アポトーシス率の増加および胸腺細胞の増殖能低下が見られた;しかし、メラトニンは、アルカリ性および酸性のDNase活性の低下、アポトーシス率の低下、胸腺細胞の増殖率の上昇を引き起こした、と報告している。
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To examine the effect of a melatonin administration on oxidative stress parameters, DNA fragmentation, apoptosis and proliferation of thymocytes in microwave-exposed rats.
4 groups of rats were examined: 1.) sham exposure, treated with saline injection, 2.) sham exposure, injection of 2 mg melatonin per kg body weight, 3.) exposure and 4.) exposure, injection of 2 mg melatonin per kg body weight (21 rats per group). After 20, 40 and 60 days, seven animals of each group were anesthetized and killed after removing the thymus.
周波数 | 900 MHz |
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タイプ |
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特性 |
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ばく露時間 | continuous for 4 hours/day on 20, 40 or 60 consecutive days |
ばく露の発生源/構造 |
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ばく露装置の詳細 | mobile phone was placed in a small perforated polycarbonated box in the center of the cage; seven freely moving rats per cage were placed on absorbing material made of rubber with wooden isolation surface |
Sham exposure | A sham exposure was conducted. |
Additional information | exposure was performed in the same room where all animals were housed or in another room (remark EMF-Portal: contradictory statements) |
In the exposed groups without melatonin (after 20, 40 and 60 days), the level of lipid peroxidation and protein oxidation, as well as the enzyme activities of catalase, xanthine oxidase, DNAse I and DNAse II were significantly increased compared to the control group. An administration of melatonin prevented these effects in the exposed group (except for the protein oxidation after 20 and 40 days).
The number of apoptotic cells was significantly increased in the exposed groups without melatonin compared to the control group. Moreover, the number of apoptotic cells increased with longer exposure duration. An administration of melatonin significantly reduced the apoptosis rate in the exposed group. The proliferation of the thymocytes was significantly decreased in the exposed groups without melatonin in comparison to the control group. This effect was stronger the longer the rats had been exposed. An administration of melatonin significantly increased the proliferation rate in the exposed group when compared to the exposed group without melatonin injection.
The authors conclude that melatonin could have a protective effect against oxidative stress and could modulate processes of apoptosis and proliferation in thymus tissue of microwave-exposed rats.
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