Lafleur M V, Loman H
Int J Radiat Biol Relat Stud Phys Chem Med. 1982 Mar;41(3):295-302. doi: 10.1080/09553008214551751.
The competition between biologically active single-stranded phiX174 DNA and the anoxic radiosensitizers metronidazole, misonidazole, paranitroacetophenone or nifuroxime for OH radicals is studied. The results are compared with experiments in which the protection of the DNA by t-butanol is determined. Also the effects of the sensitizers on the chemical nature of the damage (immediate and potential break, immediate and potential base damage) is studied. It is found that in diluted aqueous solutions of DNA these radiosensitizers do not sensitize with respect to the biological inactivation. The only effect observed is a shift from potential to immediate breaks with misonidazole and also nifuroxime.
研究了具有生物活性的单链φX174 DNA与缺氧放射增敏剂甲硝唑、米索硝唑、对硝基苯乙酮或硝呋肟对羟基自由基的竞争。将结果与测定叔丁醇对DNA保护作用的实验进行了比较。还研究了增敏剂对损伤化学性质(即时和潜在断裂、即时和潜在碱基损伤)的影响。发现在DNA的稀水溶液中,这些放射增敏剂对生物失活不具有增敏作用。观察到的唯一效应是米索硝唑和硝呋肟会使潜在断裂转变为即时断裂。