[红霉素及其顺磁类似物对DNA合成的影响]。

Antibiotiki Pub Date : 1984-06-01
L Iu Dederer, L B Gorbacheva
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引用次数: 0

摘要

Ruboxyl是一种顺磁性的红霉素类似物,在苏联科学院化学物理研究所合成并进行了初步研究。该药物具有抗肿瘤活性高、谱宽、全身毒性和心脏毒性低的特点。这是首次在DNA复制水平上对红霉素、红波基和硝基自由基进行比较生化研究的尝试。研究了这些药物对小鼠白血病细胞P-388、骨髓和心脏DNA合成的影响。结果表明,肿瘤细胞DNA合成抑制的程度和持续时间与药物的抗肿瘤活性密切相关。在给药后第3天,红霉素和红波基诱导骨髓细胞DNA合成的刺激。这可能是由于增殖细胞的细胞毒性损伤导致部分骨髓细胞从Go期转移。骨髓中的DNA合成刺激很可能与药物的毒性作用有关。心脏毒性与抑制小鼠心脏细胞DNA合成无相关性。硝基自由基对该模型无生物活性。用硝基自由基治疗的小鼠的平均寿命与对照动物相同。在肿瘤携带者中,随着肿瘤的发展,2- 14c -胸腺嘧啶在肿瘤、骨髓和心脏DNA中的结合减少。
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[Effect of rubomycin and its paramagnetic analog on DNA synthesis].

Ruboxyl, a paramagnetic analog of rubomycin, was synthesized and subjected to a preliminary investigation at the Institute of Chemical Physics of the Academy of Sciences of the USSR. The drug is characterized by a higher antitumor activity, broader spectrum and lower general and cardiac toxicity. This is the first attempt of comparative biochemical investigation of rubomycin, ruboxyl and the nitroxyl radical at the level of DNA replication. The effect of these drugs on the synthesis of DNA in the cells of leukemia P-388, the bone marrow and heart of mice was studied. It was shown that the degree and duration of the DNA synthesis inhibition in the tumor cells correlated well with the antitumor activity of the drugs. On the 3rd day after administration rubomycin and ruboxyl induced stimulation of the DNA synthesis in the cells of the bone marrow. This might be explained by transfer of a part of the population of the bone marrow cells from Go phase due to the cytotoxic damages of the proliferating cells. The DNA synthesis stimulation in the bone marrow was most likely associated with the toxic effect of the drugs. No correlation between the cardiotoxicity and inhibition of the DNA synthesis in the heart cells of the mice was observed. The nitroxyl radical showed no biological activity on this model. The average lifespan of the mice treated with the nitroxyl radical was the same as that of the control animals. A decrease in the incorporation of 2-14C-thymidine into DNA of the tumor, bone marrow and heart was observed in the tumor carriers with development of the tumor.

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