Skov K A
Radiat Res. 1984 Sep;99(3):502-10.
Using the radioprotector dimethylsulfoxide, DMSO, as a scavenger of hydroxyl radicals, the proportions of DNA damage caused by OH. were determined in mammalian cells irradiated in hypoxia with or without the radiosensitizers misonidazole and TAN or in air. Yields of both single-strand breaks (SSB) and base/sugar damage (MLS for Micrococcus luteus sensitive sites) were measured for each situation. Most of the damage enhanced by the sensitizers was found to be OH. dependent, for both MLS and SSB classes of damage: most breaks (greater than 80%) enhanced by oxygen and about two-thirds of the breaks enhanced by misonidazole (hypoxia) occur at OH.-damaged sites; most if not all base/sugar damage enhanced by the sensitizers misonidazole and TAN (in hypoxia) occurs only in the presence of OH., whereas in air, some (about one-quarter) of the enhanced MLS damage does not require OH.. The sensitizer enhancement ratios in the presence of scavenger and the degree of protection afforded by the scavenger determined for total (MLS + SSB) damage agree well with those derived from corresponding survival experiments.
使用辐射防护剂二甲基亚砜(DMSO)作为羟基自由基的清除剂,测定了在缺氧条件下照射的哺乳动物细胞中,有或没有放射增敏剂米索硝唑和TAN时,以及在空气中照射时,由羟基自由基(OH.)引起的DNA损伤比例。针对每种情况,测量了单链断裂(SSB)和碱基/糖损伤(对藤黄微球菌敏感位点的MLS)的产额。发现增敏剂增强的大部分损伤对于MLS和SSB两类损伤而言都依赖于OH.:氧气增强的大多数断裂(超过80%)以及米索硝唑(缺氧条件下)增强的约三分之二的断裂发生在OH.损伤的位点;米索硝唑和TAN(缺氧条件下)这两种增敏剂增强的大部分(如果不是全部)碱基/糖损伤仅在有OH.的情况下发生,而在空气中,增强的MLS损伤中有一些(约四分之一)不需要OH.。清除剂存在时的增敏剂增强比率以及清除剂对总损伤(MLS + SSB)提供的保护程度与相应存活实验得出的结果非常吻合。