Oblapenko N G, Loknitskaia N N, Presnova Zh F, Chernov V A, Fonshteĭn L M
Genetika. 1986 Sep;22(9):2265-71.
The effect of transplantation of rat tumours Jensen sarcoma, sarcoma 45, sarcoma M-1, as well as of inoculation of rat normal connective tissue on the processes of biotransformation of antitumour preparations cyclophosphane (CP), thiophosphamide, prospidine and of model compound nitrosomorpholine (NM) was studied. The study was accomplished by means of the Ames test with indicator bacterial strain Salmonella typhimurium TA 1950 in relation to the reactions of the 1st and the 2nd phases of xenobiotics metabolism. It was shown that the presence of tumours leads to inhibition of both metabolic activation processes of the promutagens NM and CP and the conjugation reactions of genetically active metabolites of these compounds with reduced glutathione. Genetic danger is supposed to be increased during application of antitumour preparations, the mutagenic activity of which is due to the activity of their metabolites. It is noted that the most essential effect on biotransformation processes of NM and CP was exhibited by sarcoma M-1, the most important changes of the biotransformation processes of promutagens being observed in the initial period of pathologic process, i.e. on the 3rd day after inoculation. Transplantation of the normal connective tissue of rats had no effect on reactions of both the 1st and the 2nd phase of metabolism of the promutagens studied.
研究了大鼠肿瘤(詹森肉瘤、肉瘤45、肉瘤M-1)移植以及大鼠正常结缔组织接种对抗肿瘤制剂环磷酰胺(CP)、硫磷酰胺、丙脒腙和模型化合物亚硝基吗啉(NM)生物转化过程的影响。该研究通过艾姆斯试验,使用指示菌株鼠伤寒沙门氏菌TA 1950,针对外源化合物代谢第一和第二阶段的反应来完成。结果表明,肿瘤的存在导致前诱变剂NM和CP的代谢活化过程以及这些化合物的遗传活性代谢物与还原型谷胱甘肽的结合反应均受到抑制。在应用其诱变活性归因于代谢物活性的抗肿瘤制剂时,遗传风险可能会增加。值得注意的是,肉瘤M-1对NM和CP的生物转化过程影响最为显著,在前诱变剂生物转化过程中观察到的最重要变化出现在病理过程的初期,即在接种后的第3天。大鼠正常结缔组织的移植对所研究的前诱变剂代谢第一和第二阶段的反应均无影响。