Harrison S D, Denine E P, Peckham J C
Cancer Treat Rep. 1978 Apr;62(4):533-45.
Qualitative and quantitative toxicity studies were conducted in BDF mice after ip injection of 33, 66, 134, and 200 mg/kg of 5-fluorouracil (5-FU) in daily doses for 1, 2, 3, or 4 consecutive days. Groups of five mice from each schedule and dose level provided blood and selected visceral organs for hematologic and histologic evaluation on posttreatment Days 1, 3, 6, 10, 14, and 21. Comparable groups of five mice were blood donors for biochemical evaluation of pooled plasma samples. The results indicated the onset, severity, and duration of injury to target organs and characterized the relationship of sublethal toxicity to drug dose and frequency of administration. Marrow suppression was reflected in peripheral erythropenia, thrombocytopenia, and leukopenia and also in medullary erythropenia and granulocytopenia. A transient elevation of plasma LDH, loss of body weight, and appearance of microscopic lesions of the gastrointestinal mucosae were additional indices of toxicity. The BDF mouse appears to provide a good qualitative and quantitative prediction of 5-FU toxicity, although the mouse apparently is quantitatively more sensitive than man.
对BDF小鼠进行了定性和定量毒性研究,经腹腔注射33、66、134和200mg/kg的5-氟尿嘧啶(5-FU),每日给药一次,连续给药1、2、3或4天。每个给药方案和剂量水平的五组小鼠在治疗后第1、3、6、10、14和21天提供血液和选定的内脏器官用于血液学和组织学评估。五组可比的小鼠作为供血者,用于对混合血浆样本进行生化评估。结果表明了靶器官损伤的起始、严重程度和持续时间,并描述了亚致死毒性与药物剂量和给药频率之间的关系。骨髓抑制表现为外周血红细胞减少、血小板减少和白细胞减少,也表现为骨髓红细胞减少和粒细胞减少。血浆乳酸脱氢酶短暂升高、体重减轻以及胃肠道黏膜出现微观病变是毒性的其他指标。BDF小鼠似乎能对5-FU毒性进行良好的定性和定量预测,尽管小鼠在定量方面显然比人类更敏感。