Koch C J, Stobbe C C, Bump E A
Radiat Res. 1984 Apr;98(1):141-53.
Pretreatment of V79- WNRE cells with 150 microM diethylmaleate for 1 hr at 37 degrees C caused a decrease in intracellular glutathione levels to approximately 10-15% of control levels (0.5 vs 5.0 nmol/10(6) cells). The cells could be washed free of diethylmaleate and held at 0 degree C for several hours without toxicity and with no increase in glutathione concentration, although the glutathione concentration rapidly increased to normal levels at higher temperatures. Survival curves were determined as a function of oxygen or misonidazole concentration (the latter in the absence of oxygen). A new "thin-film" technique was used to avoid changes in oxygen concentration because of radiochemical or cellular oxygen consumption. Glutathione depletion itself caused a small but consistent radiosensitization of hypoxic cells (dose enhancement ratio of 1.2). However, glutathione depletion caused a profound change in the radiosensitizing efficiency of misonidazole, with a decrease in Km of about sevenfold from 0.6 to 0.09 mM. In contrast, only a 2.5-fold decrease was found in the Km for radiosensitization by oxygen with diethylmaleate pretreatment. These results suggest a fundamental problem with the conventional theory of radiosensitivity whereby one considers a first-order competition for reaction with target radicals between radical-fixing versus radical-repairing species. It also suggests difficulties in the interpretation of glutathione as the only endogenous protective species.
用150微摩尔的马来酸二乙酯在37摄氏度下对V79 - WNRE细胞进行预处理1小时,导致细胞内谷胱甘肽水平降至对照水平的约10 - 15%(0.5纳摩尔/10⁶细胞对5.0纳摩尔/10⁶细胞)。细胞可以用马来酸二乙酯清洗干净,并在0摄氏度下保存数小时而无毒性且谷胱甘肽浓度无增加,尽管在较高温度下谷胱甘肽浓度会迅速恢复到正常水平。根据氧气或米索硝唑浓度(后者在无氧条件下)测定存活曲线。采用一种新的“薄膜”技术以避免由于放射化学或细胞耗氧导致的氧气浓度变化。谷胱甘肽耗竭本身导致低氧细胞有轻微但一致的放射增敏作用(剂量增强比为1.2)。然而,谷胱甘肽耗竭导致米索硝唑的放射增敏效率发生深刻变化,其米氏常数(Km)从0.6毫摩尔降至0.09毫摩尔,下降了约7倍。相比之下,经马来酸二乙酯预处理后,氧气放射增敏的米氏常数仅下降了2.5倍。这些结果提示了传统放射敏感性理论存在一个根本问题,即人们认为在自由基固定与自由基修复物种之间存在与靶自由基反应的一级竞争。这也提示了将谷胱甘肽视为唯一内源性保护物种在解释上的困难。