N-(1-萘基)二盐酸乙二胺可能致癌性的生物测定。

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引用次数: 0

摘要

采用Fischer 344大鼠和B6C3F1小鼠进行了N-(1-萘基)乙二胺二盐酸可能致癌性的生物测定。将N-(1-萘基)乙二胺二盐酸盐以两种浓度中的任意一种加入饲料中,每组50只雄性和50只雌性动物。雌雄各25只大鼠和雌雄各50只小鼠作为对照。给大鼠和雄性小鼠的饲料N-(1-萘基)乙二胺的高、低浓度分别为0.1%和0.05%。给雌性小鼠的高、低时间加权平均浓度分别为0.3%和0.2%。给药104周,高剂量大鼠观察4周,低剂量大鼠、低剂量雌性小鼠、高剂量雌性小鼠观察3周,高剂量雄性小鼠观察1周。给药的N-(1-萘基)乙二胺的浓度与雌雄大鼠或雄性小鼠的死亡率之间没有显著的正相关。在雌性小鼠中,浓度与死亡率呈显著正相关。在所有组中,除了高剂量的雌性外,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,大鼠和小鼠的平均体重明显下降,这表明这些动物无法忍受更高浓度的测试化学物质。在大鼠或小鼠中,N-(1-萘基)二盐酸乙二胺浓度与肿瘤发生率之间无统计学意义的正相关。在本生物试验条件下,对Fischer 344大鼠和B6C3F1小鼠膳食给予N-(1-萘基)乙二胺二盐酸盐无致癌性。
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Bioassay of N-(1-naphthyl)ethylenediamine dihydrochloride for possible carcinogenicity.

A bioassay for the possible carcinogenicity of N-(1-naphthyl)ethylenediamine dihydrochloride was conducted using Fischer 344 rats and B6C3F1 mice. N-(1-Naphthyl)ethylenediamine dihydrochloride was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species. Twenty-five rats of each sex and 50 mice of each sex were placed on test as controls. The high and low dietary concentrations of N-(1-naphthyl)ethylenediamine dihydrochloride administered to rats and male mice were 0.1 and 0.05 percent, respectively. The high and low time-weighted average concentrations administered to female mice were, respectively, 0.3 and 0.2 percent. The compound was administered in the diet for 104 weeks, followed by an observation period of 4 weeks for high dose rats, 3 weeks for low dose rats, low dose female mice, and high dose female mice, and 1 week for high dose male mice. There were no significant positive associations between the concentrations of N-(1-naphthyl)ethylenediamine dihydrochloride administered and mortality in rats of either sex or in male mice. There was a significant positive association between concentration and mortality in female mice. In all groups, except for high dose females, adequate numbers of animals survived sufficiently long to be at risk from late-developing tumors. Mean body weight depression, in relation to controls, was apparent for both sexes of rats and mice, indicating that higher concentrations of the test chemical would not have been tolerated by these animals. In rats or mice of either sex, there were no statistically significant positive associations between the concentration of N-(1-naphthyl)ethylenediamine dihydrochloride and tumor incidence. Under the conditions of this bioassay, dietary administration of N-(1-naphthyl)ethylenediamine dihydrochloride was not carcinogenic in Fischer 344 rats or B6C3F1 mice.

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