Horsman M R, Stratford I J
Chem Biol Interact. 1982 Aug;41(2):193-201. doi: 10.1016/0009-2797(82)90089-8.
Caffeine was found to potentiate the cytotoxic effect of misonidazole (1-(2-nitroimidazol-1-yl)-3-methoxy-2-propanol) towards mammalian cells in vitro. This enhancement of toxicity is shown to occur under both aerobic and hypoxic conditions. Split dose experiments indicate that the general shape of the hypoxic survival curve can be restored by exposure of cells of O2 between doses. Exposure of cells to 2mM caffeine during the split dose experiment has no potentiating effect. Further experiments showed that caffeine affects the expression of misonidazole-induced potentially lethal damage. Other electron-affinic nitro compounds which show greater toxicity to hypoxic compared to aerobic cells, viz. metronidazole and nitrofurantoin, also have their toxicities enhanced by subsequent exposure to caffeine.
研究发现,咖啡因可增强米索硝唑(1-(2-硝基咪唑-1-基)-3-甲氧基-2-丙醇)在体外对哺乳动物细胞的细胞毒性作用。这种毒性增强作用在有氧和缺氧条件下均会出现。分次给药实验表明,在两次给药之间让细胞暴露于氧气中,可恢复缺氧存活曲线的总体形状。在分次给药实验中,将细胞暴露于2mM咖啡因下没有增强作用。进一步的实验表明,咖啡因会影响米索硝唑诱导的潜在致死性损伤的表达。其他对缺氧细胞毒性比对有氧细胞更大的亲电子硝基化合物,即甲硝唑和呋喃妥因,在随后暴露于咖啡因后其毒性也会增强。