氯丙胺可能致癌性的生物测定。

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摘要

将氯丙胺的实验材料加入饲料中,对Fischer 344大鼠和B6C3F1小鼠进行致癌性生物测定。每组35只大鼠和35只小鼠按如下方式服用氯丙胺:大鼠每周服用5天,浓度为3000或6000 ppm,持续103至105周;小鼠每周服用5天,浓度为5000或10000 ppm,持续34周;随后服用70周,浓度为2500或5000 ppm。低剂量雄性和雌性小鼠的时间加权平均剂量为3317 ppm,高剂量雄性和雌性小鼠的时间加权平均剂量为6635 ppm。配对的对照组由各组各15只未治疗的大鼠和15只未治疗的小鼠组成。所有存活的大鼠和小鼠在103至105周时被杀死。在整个研究过程中,低剂量和高剂量大鼠的平均体重都低于匹配的对照组。在小鼠中,由于高剂量组的早期死亡,剂量在第34周减少;经过这种调整后,实验组的老鼠体重增加了,但体重从未达到对照组的体重。治疗大鼠和低剂量小鼠的存活率足以对肿瘤发生率进行有意义的统计分析。在大鼠和小鼠中,与匹配的对照组相比,治疗组的肿瘤发病率没有显著增加。结论在本实验条件下,氯丙胺对Fischer 344大鼠和B6C3F1小鼠无致癌性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioassay of chlorpropamide for possible carcinogenicity.

A bioassay of chlorpropamide for possible carcinogenicity was conducted by administering the test material in feed to Fischer 344 rats and B6C3F1 mice. Groups of 35 rats and 35 mice of each sex were administered chlorpropamide as follows: rats 5 days per week for 103 to 105 weeks at 3,000 or 6,000 ppm, and mice 5 days per week for 34 weeks at 5,000 or 10,000 ppm, followed by 70 weeks at 2,500 or 5,000 ppm. The time-weighted average doses for mice were 3,317 ppm for low-dose males and females, and 6,635 ppm for high-dose males and females. Matched controls consisted of groups of 15 untreated rats and 15 untreated mice of each sex. All surviving rats and mice were killed at 103 to 105 weeks. Mean body weights of both low- and high-dose rats were lower than those of the matched controls throughout the study. In mice, doses were reduced at week 34, due to early deaths in the high-dose groups; following this adjustment the treated mice gained weight, but the weights never reached those of the controls. Survival of the treated rats and the low-dose mice was adequate for meaningful statistical analyses of the incidences of tumors. In both rats and mice, the incidences of tumors among the treated groups were not significantly increased in comparison with matched controls. It is concluded that under the conditions of this bioassay, chlorpropamide was not carcinogenic for Fischer 344 rats or B6C3F1 mice.

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