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首页> 外文期刊>Luminescence: The journal of biological and chemical luminescence >Evaluation of the degree of medical radiation damage with a highly sensitive chemiluminescence method
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Evaluation of the degree of medical radiation damage with a highly sensitive chemiluminescence method

机译:用高灵敏度化学发光法评估医学辐射损伤的程度

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摘要

A highly sensitive chemiluminescence (CL) method for evaluation of medical radiation damage degree is presented. According to the principle of cell stress response to ionizing radiation, lymphocytes will produce reactive oxygen species (ROS) after irradiation. The ROS produced can react with 2-methyl-6-(p-methoxyphenyl)-3,7-dihydroimidazo[1,2-alpha] pyrazin-3-one (MCLA), a specific CL probe for superoxide anion (O-2(.-)) and singlet oxygen (O-1(2)), to emit light at 465 nm. The CL intensity is positively related to the amount of generated ROS detected 30 min after irradiation. Cell viability, which is inversely related to cell mortality, was determined by MTT assay after 3 days' culture. The results show that both CL intensity and cell mortality of lymphocytes increase with the increase of the radiation dose when the dosage is no more than 3 Gy, suggesting a positive relationship between the degree of lymphocyte cell damage and the amount of ROS generated. In addition, the effects of catalase, Cu-Zn superoxide dismutase (SOD), mannitol, sodium azide (NaN3), and D2O on MCLA-dependent CL of lymphocytes are discussed. We believe that the MCLA-dependent CL method would potentially provide an easy way for evaluating the degree of lymphocyte damage induced by radiation. Copyright (C) 2004 John Wiley Sons, Ltd.
机译:提出了一种用于评估医学辐射损伤程度的高灵敏度化学发光(CL)方法。根据细胞对电离辐射的应激反应原理,淋巴细胞在辐射后会产生活性氧(ROS)。产生的ROS可以与2-甲基-6-(对甲氧基苯基)-3,7-二氢咪唑并[1,2-α吡嗪-3-酮(MCLA)反应,MCLA是一种超氧阴离子的特异CL探针(O-2 (.-))和单线态氧(O-1(2))发出465 nm的光。 CL强度与照射后30分钟检测到的ROS的生成量呈正相关。培养3天后,通过MTT法测定与细胞死亡率成反比的细胞活力。结果表明,当辐射剂量不超过3 Gy时,淋巴细胞的CL强度和细胞死亡率均随辐射剂量的增加而增加,表明淋巴细胞损伤程度与ROS的产生呈正相关。此外,还讨论了过氧化氢酶,铜锌超氧化物歧化酶(SOD),甘露醇,叠氮化钠(NaN3)和D2O对淋巴细胞MCLA依赖性CL的影响。我们认为,依赖MCLA的CL方法可能会提供一种简便的方法来评估辐射引起的淋巴细胞损伤程度。版权所有(C)2004 John Wiley Sons,Ltd.

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