硝芬可能致癌性的生物测定。

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引用次数: 0

摘要

用奥斯本-孟德尔大鼠和B6C3F1小鼠进行了工业级硝芬可能致癌性的生物测定。在饲料中加入两种浓度的硝基芬,每组50只雄性和50只雌性动物。雄性大鼠的时间加权平均高、低浓度分别为3656 ppm和2300ppm,雌性大鼠为2600 ppm和1300ppm,雄性和雌性小鼠分别为4696 ppm和2348 ppm。78周治疗期结束后,低剂量和对照雄性和所有雌性大鼠继续观察32周;高剂量雄性大鼠继续观察4周。在78周的治疗期后,对所有小鼠进行了额外的12周观察。每个物种各取20只雌雄动物作为对照进行试验。他们的饮食中没有添加硝芬。雌性大鼠胰脏癌的发病率与饮食中硝芬的浓度有统计学意义的正相关。与对照组相比,高剂量雌性大鼠的肿瘤发生率显著。与化学毒性相关的低存活率妨碍了对雄性大鼠硝芬致癌性的评估。在两性小鼠中,与对照组相比,高剂量和低剂量水平的肝细胞癌发病率都非常显著。在两性小鼠中,肝脏血管肉瘤的发病率与饮食中硝芬的浓度有统计学意义的关系,与对照组相比,高剂量雄性小鼠的发病率显著。本研究结果表明,口服技术级硝芬在B6C3F1小鼠和雌雄小鼠中都是一种肝癌致癌物。硝芬对雌性奥斯本-孟德尔大鼠也有致癌性。
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Bioassay of nitrofen for possible carcinogenicity.

A bioassay of technical-grade nitrofen for possible carcinogenicity was conducted using Osborne-Mendel rats and B6C3F1 mice. Nitrofen was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species. The time-weighted average high and low dietary concentrations of nitrofen were 3,656 and 2,300 ppm for male rats, 2,600 and 1,300 ppm for female rats, and 4,696 and 2,348 ppm for both male and female mice, respectively. After a 78-week treatment period, observation of the low dose and control male and all female rats continued for an additional 32 weeks; observation of the high dose male rats continued for an additional 4 weeks. All mice were observed for an additional 12 weeks after the 78-week treatment period. For each species, 20 animals of each sex were placed on test as controls. No nitrofen was added to their diet. The incidence of carcinomas of the pancreas had a statistically significant positive association with concentration of nitrofen in the diet of female rats. The incidence of this tumor in high dose female rats was significant when compared to controls. Poor survival related to chemical toxicity precluded the evaluation of the carcinogenicity of nitrofen in male rats. In mice of both sexes, the incidence of hepatocellular carcinoma at both high and low dose levels was highly significant when compared to the controls. The incidence of hemangiosarcoma of the liver had a statistically significant relationship with nitrofen concentration in the diet for mice of both sexes, and the incidence in high dose male mice was significant when compared to controls. The results of this study indicate that orally administered technical-grade nitrofen is a liver carcinogen in B6C3F1 mice of both sexes. Nitrofen is also carcinogenic to female Osborne-Mendel rats.

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