5-氟尿嘧啶及其前药5'-脱氧-5-氟吡啶在大鼠体内的生物活性。

J L Au, Y M Rustum, H K Slocum
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引用次数: 3

摘要

比较了5-氟尿嘧啶(FUra)和5'-脱氧-5-氟吡啶(dFUR)对携带二甲肼诱导的移植结肠肿瘤的雌性Fischer大鼠的抗肿瘤活性和毒性。FUra和dFUR的治疗效果不受初始肿瘤大小的影响,但取决于剂量和治疗时间。用35 mg-kg-1-day-1 FUra或500 mg-kg-1-day-1 dFUR输注7 d,最大有效率为80-90%。FUra和dFUR对荷瘤大鼠和正常大鼠的宿主毒性包括胃肠道和中枢神经系统紊乱。毒性相关死亡之前,动物体重减轻20%以上,并出现其他胃肠道紊乱迹象。FUra的最大治疗剂量与引起正常大鼠40%死亡的中毒剂量相同。而dFUR的最大治疗剂量未引起中毒性死亡,dFUR的阈值致死剂量比最大治疗剂量高40%,表明dFUR对该大鼠肿瘤有较好的治疗指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biological activities of 5-fluorouracil and its prodrug 5'-deoxy-5-fluorouridine in rats.

The antitumor activity and toxicity of 5-fluorouracil (FUra) and 5'-deoxy-5-fluorouridine (dFUR) were compared in female Fischer rats bearing transplanted dimethylhydrazine-induced colon tumors. The therapeutic effects of FUra and dFUR were not affected by the initial tumor size, but were dependent on the dose and duration of treatment. The maximal response rate of 80-90% cures was obtained with 7-day infusions of 35 mg-kg-1-day-1 FUra or 500 mg-kg-1-day-1 dFUR. The host toxicity of FUra and dFUR in tumor-bearing or normal rats included gastrointestinal and central nervous system disturbances. Toxicity related death was preceded by a greater than 20% animal weight loss and other signs of gastrointestinal disturbances. The maximal therapeutic dose of FUra was identical to the toxic dose which caused 40% death in normal rats. By contrast, the maximal therapeutic dose of dFUR did not cause toxic death, and the threshold lethal dose of dFUR was 40% higher than the maximally therapeutic dose, indicating a better therapeutic index for dFUR in this rat tumor.

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