β -胡萝卜素对某些抗肿瘤药物致突变活性的影响。

Acta vitaminologica et enzymologica Pub Date : 1985-01-01
A Belisario, N Panza, G Pacilio
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引用次数: 0

摘要

研究了几种细胞抑制剂在无-胡萝卜素和有-胡萝卜素的情况下对鼠伤寒沙门菌的致突变活性。类维甲酸在体外和体内均能降低环磷酰胺的致突变性。相反,其代谢物4'-羟基环磷酰胺不需要酶转化来发挥对细菌的遗传毒性活性,不受β -胡萝卜素存在的影响。此外,典型的直接作用诱变剂顺铂、阿霉素和4′表阿霉素的诱变活性不受β -胡萝卜素的影响。获得的数据证实,β -胡萝卜素能够通过干扰环磷酰胺的代谢激活来阻止其致突变活性,但无法抑制基因毒性化合物与细菌DNA的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of beta-carotene on mutagenic activity of some antineoplastics.

Mutagenic activity on Salmonella typhimurium strains of some cytostatic drugs in the absence and in the presence of beta-carotene was evaluated. Cyclophosphamide mutagenicity was reduced by the retinoid both in vitro and in vivo. Conversely, its metabolite 4'-hydroxy-cyclophosphamide, which does not require enzymatic transformation to exert genotoxic activity against bacteria, was not affected by the presence of beta-carotene. Moreover, the mutagenic activity of cis-Platinum, Adriamycin and 4'Epiadriamycin, which are typical direct-acting mutagens, was not affected by beta-carotene. Data obtained confirm that beta-carotene is able to prevent mutagenic activity of cyclophosphamide by interfering with its metabolic activation but failed to inhibit the interaction of genotoxic compounds with bacterial DNA.

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