Elisova T V, Feoktistova T P, Stavrakova N M
Radiobiologiia. 1988 Sep-Oct;28(5):617-22.
A study was made of the effect of two-hour treatment of Chinese hamster cells with cytosine arabinoside (AraC) combined with hydroxyurea (HU) at the G1 phase of the cell cycle on lethal and mutagenic effects of X-radiation (50 to 400 cGy). The inhibitors were shown to increase a spontaneous mutation level of the resistance to 6-thioguanine: this increase augmented by 3 times as the time the treatment increased from 1-2 to 6 h. However, while sharply enhancing the inactivating effect of X-radiation (the enhancement coefficient was 2.6) Arac+HU caused an additive, or a somewhat lesser, effect as estimated by the yield of mutations. It is suggested that AraC combined with hydroxyurea fail to modify the radiation-induced premutation damages.
研究了在细胞周期的G1期用阿糖胞苷(AraC)联合羟基脲(HU)对中国仓鼠细胞进行两小时处理,对X射线(50至400 cGy)的致死和诱变效应的影响。结果表明,这些抑制剂会增加对6-硫鸟嘌呤抗性的自发突变水平:随着处理时间从1 - 2小时增加到6小时,这种增加幅度增大了3倍。然而,虽然阿糖胞苷+羟基脲急剧增强了X射线的灭活作用(增强系数为2.6),但根据突变产量估计,其诱变效应是相加的,或者略小。有人认为,阿糖胞苷与羟基脲联合使用不能改变辐射诱导的前突变损伤。