1-苯基-3-甲基-5-吡唑酮可能致癌性的生物测定。

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摘要

采用Fischer 344大鼠和B6C3F1小鼠对1-苯基-3-甲基-5-吡唑酮进行了可能致癌性的生物测定。将1-苯基-3-甲基-5-吡唑酮以两种浓度中的任意一种添加到饲料中,每组49或50只雄性动物和50只雌性动物。大鼠使用的高、低浓度1-苯基-3-甲基-5-吡唑啉酮分别为5000 ppm和2500 ppm,小鼠使用的高、低浓度分别为15000 ppm和7500 ppm。每个物种和性别各20只动物作为对照进行试验。给药103周后,大鼠再加2周观察期。给药102周后,再对小鼠进行2周的观察。在这两个物种中,有足够数量的动物存活了足够长的时间,从而有可能患上晚期肿瘤。在小鼠中观察到化合物相关的平均体重下降,但在大鼠中没有。此外,大鼠饮食中服用1-苯基-3-甲基-5-吡唑啉酮并没有明显加速死亡或其他毒性迹象;因此,该化合物可能没有以最大耐受浓度给予大鼠。在大鼠和小鼠的性别中,没有肿瘤在化学药物给药和发病率之间建立显著的正相关关系。在本实验条件下,1-苯基-3-甲基-5-吡唑酮对Fischer 344大鼠和B6C3F1小鼠没有致癌性。
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Bioassay of 1-phenyl-3-methyl-5-pyrazolone for possible carcinogenicity.

A bioassay of 1-phenyl-3-methyl-5-pyrazolone for possible carcinogenicity was conducted using Fischer 344 rats and B6C3F1 mice. 1-Phenyl-3-methyl-5-pyrazolone was administered in the feed, at either of two concentrations, to groups of 49 or 50 male and 50 female animals of each species. The high and low concentrations of 1-phenyl-3-methyl-5-pyrazolone utilized were, respectively, 5,000 and 2,500 ppm for rats and 15,000 and 7,500 ppm for mice. Twenty animals of each species and sex were placed on test as controls. After a 103-week period of chemical administration, there was an additional observation period of 2 weeks for rats. A 102-week period of chemical administration was followed by an additional 2-week observation period for mice. In both species adequate numbers of animals survived sufficiently long to be at risk from late-developing tumors. Compound-related mean body weight depression was observed in mice, but not in rats. In addition, no significant accelerated mortality or other signs of toxicity were associated with the dietary administration of 1-phenyl-3-methyl-5-pyrazolone to rats; therefore, it is possible that the compound was not administered to rats at the maximum tolerated concentration. There were no tumors in either sex of rats or mice for which a significant positive association could be established between chemical administration and incidence. Under the conditions of this bioassay, there was no evidence for the carcinogenicity of 1-phenyl-3-methyl-5-pyrazolone to Fischer 344 rats or B6C3F1 mice.

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