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氧化还原活性化合物在耐药性 P388 白血病小鼠株治疗中的应用。

Redox-Active Compounds in the Therapy of Drug-Resistant Murine Leukemia P388 Strains.

机构信息

Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russia.

出版信息

Bull Exp Biol Med. 2024 Jun;177(2):266-270. doi: 10.1007/s10517-024-06170-4. Epub 2024 Aug 2.

Abstract

The efficiency of combinations of cytostatics cisplatin and adriamycin with antioxidant sodium 3-(3'-tert-butyl-4-hydroxyphenyl)propyl thiosulfate (TS-13), and nitric oxide (NO) donor NaNO was evaluated on two drug-resistant strains of leukemia P388 with changed redox-status of cells. Simultaneous use of both NO donor and TS-13 in combinations with the cytostatics did not increase the efficiency of therapy. In addition, antioxidant activity of TS-13, NaNO, and their combinations was studied by the method of luminol-dependent chemiluminescence on the model systems with the use of the homogenized cells of sensitive strain and two drug-resistant strains of leukemia P388. It was shown that TS-13 and NO donor produced opposite effects: TS-13 decreased, while NO donor increased the content of free radicals in the model system. Combinations of antioxidant TS-13 and NO donor should be used with consideration for the redox-status of tumor treated.

摘要

评估了细胞氧化还原状态改变的白血病 P388 两种耐药株中细胞抑制剂顺铂和阿霉素与抗氧化剂 3-(3'-叔丁基-4-羟基苯基)丙基硫代硫酸盐(TS-13)和一氧化氮(NO)供体 NaNO 的组合的效率。在细胞抑制剂联合使用两种 NO 供体和 TS-13 并没有提高治疗效率。此外,通过使用敏感株和白血病 P388 的两种耐药株的匀浆细胞的模型系统,用发光依赖性化学发光法研究了 TS-13、NaNO 及其组合的抗氧化活性。结果表明,TS-13 和 NO 供体产生相反的作用:TS-13 降低,而 NO 供体增加模型系统中自由基的含量。抗氧化剂 TS-13 和 NO 供体的组合应考虑到治疗的肿瘤的氧化还原状态来使用。

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