Dzhioev F K, Iamshanov V A
Vopr Onkol. 1975;21(4):37-40.
Rats were injected sarcolysin-H3 in a dose of 200 or 500 mC per rat. In animals sacrificed 30, 60 and 90 minutes following sarcolysin-H3 injection an increased radioactivity of DNA was noted that indicates binding of sarcolysin-H3 or its labelled derivatives to DNA. Guanine or quanosine-2', 3' monophosphate injected in animals decreased binding of sarcolysin-H3 to the rat liver DNA (maximum reduction of DNA radioactivity in 47%). In the experiments in vitro guanosine-2', 3' phosphate inhibited sarcolysin-H3 binding to DNA isolated from E. coli. A protective effect of quanine and guanosine-2', 3' phosphate with respect to DNA alkylation seems to be considerably conditioned by a competitive action of these nucleophils.
给大鼠注射剂量为每只200或500毫居里的溶肉瘤素 - H3。在注射溶肉瘤素 - H3后30、60和90分钟处死的动物中,观察到DNA放射性增加,这表明溶肉瘤素 - H3或其标记衍生物与DNA结合。给动物注射鸟嘌呤或2',3'-磷酸鸟苷可降低溶肉瘤素 - H3与大鼠肝脏DNA的结合(DNA放射性最大降低47%)。在体外实验中,2',3'-磷酸鸟苷抑制溶肉瘤素 - H3与从大肠杆菌分离的DNA结合。鸟嘌呤和2',3'-磷酸鸟苷对DNA烷基化的保护作用似乎在很大程度上取决于这些亲核试剂的竞争作用。