3-硝基对苯乙酯可能致癌性的生物测定。

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摘要

采用Fischer 344大鼠和B6C3F1小鼠进行了3-硝基对苯乙酯可能致癌性的生物测定。将3-硝基对苯乙肽以两种浓度中的任何一种加入饲料中,每组50只雄性和50只雌性动物,低剂量雄性小鼠除外,其中有49只。每个性别和物种各50只动物作为对照进行试验。大鼠的高、低时间加权平均日粮浓度分别为0.36%和0.18%,小鼠的高、低时间加权平均日粮浓度分别为1.46%和0.73%。该化合物在饮食中添加78周,随后对大鼠和小鼠进行长达30周的观察期。施用3-硝基对苯乙肽的浓度与大鼠或小鼠的死亡率之间没有显著的正相关。此外,所有组中都有足够数量的动物存活足够长的时间,从而有患晚期肿瘤的风险。与对照组相比,高剂量雄性小鼠肝细胞癌和腺瘤的发生率显著增加。与对照组相比,在任何其他剂量组中没有其他肿瘤发生显著的阳性增加。在此生物试验条件下,3-硝基-对苯乙肽对Fischer 344大鼠和雌性小鼠均无致癌性。然而,该化合物在雄性B6C3F1小鼠中被认为具有致癌性,因为在这些动物中肝细胞癌和肝细胞腺瘤的发病率显著增加。
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Bioassay of 3-nitro-p-acetophenetide for possible carcinogenicity.

A bioassay for possible carcinogenicity of 3-nitro-p-acetophenetide was conducted using Fischer 344 rats and B6C3F1 mice. 3-Nitro-p-acetophenetide was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species, with the exception of low dose male mice, of which there were 49. Fifty animals of each sex and species were placed on test as controls. The high and low time- weighted average dietary concentrations of 3-nitro-p-acetophenetide were, respectively, 0.36 and 0.18 percent for rats and 1.46 and 0.73 percent for mice. The compound was administered in the diet for 78 weeks, followed by an observation period of up to 30 weeks for rats and 20 weeks for mice. There were no significant positive associations between the concentrations of 3-nitro-p-acetophenetide administered and mortality in rats or mice of either sex. In addition, adequate numbers of animals in all groups survived sufficiently long to be at risk from late-developing tumors. There was a statistically significant increased incidence of a combination of hepatocellular carcinomas and adenomas when high dose male mice were compared to controls. No other neoplasm in any other dosed group occurred in significant positive increased incidences when compared to controls. Under the conditions of this bioassay, dietary administration of 3-nitro-p-acetophenetide was not carcinogenic in Fischer 344 rats of either sex or in female mice. The compound, however, was considered carcinogenic in male B6C3F1 mice based on a significant increase in the combined incidence of hepatocellular carcinomas and hepatocellular adenomas in these animals.

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