[抗亚硝化系统作为恶性肿瘤抵抗一氧化氮细胞毒作用的一个因素]。

Biofizika Pub Date : 2015-01-01
A F Vanin, L A Ostrovskaia, D B Korman, V D Miloian, L N Kubrina, M M Borodulin, M M Fomina, N V Bliukhterova, V A Rykova
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引用次数: 0

摘要

双核二硝基铁配合物与谷胱甘肽对Lewis肺癌BDF1小鼠移植实体瘤的生长有抑制作用。小鼠腹腔注射双核二硝基铁配合物,剂量为200 μM/kg,第1 ~ 5天和第7 ~ 11天。双核二硝基铁配合物:游离谷胱甘肽比例为1:1;在1:10溶液中,dnic的抑制效果分别达到70%和85%。当不进一步输注b - dnic时,观察到肿瘤生长强烈,肿瘤生长速度比对照组快。用EPR法检测肿瘤中dnic和含血红素蛋白的亚硝基铁复合物的选择性积累。后者也在对照动物的肿瘤中发现。小鼠B-DNIC给药过程中肿瘤生长的延迟可能是由于肿瘤组织对B-DNIC释放的NO的作用产生了抗亚硝化防御。
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[Anti-nitrosative system as a factor of malignant tumor resistance to cytotoxic effect of nitrogen monooxide].

The inhibitory action of binuclear dinitrosyl iron complexes with glutathione on the growth of implanted solid tumor in BDF1 mice bearing Lewis lung carcinoma cells was found. The effect was induced by intraperitoneal injection of the binuclear dinitrosyl iron complexes to mice at a dose of 200 μM/kg daily on days 1-5 and 7-11. At the binuclear dinitrosyl iron complexes: free glutathione ratios of 1:1; and 1:10 in solutions, the inhibitory effect of the DNICs reached the level of 70% and 85%, respectively. When B-DNICs were not further infused, intensive tumor growth, a more rapid rate of tumor growth than control, was observed. The selective accumulation of DNICs as well as iron nitrosyl complexes of heme-containing proteins in tumors were detected by EPR method. The latter were found also in the tumors in control animals. Tumor growth delay in course of B-DNIC administration to the mice is supposed to be due to the elaboration of anti-nitrosative defense in tumor tissue in response to the action of NO released from B-DNIC.

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