Bioassay of 2,3,5,6-tetrachloro-4-nitroanisole for possible carcinogenicity (CAS No. 2438-88-2).

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Abstract

A bioassay for possible carcinogenicity of 2,4,5,6-tetrachloro-4-nitroanisole was conducted using Fischer 344 rats and B6C3F1 mice. 2,3,5,6-Tetrachloro-4-nitroanisole was administered in the feed, at either of two concentrations, to groups of male and female animals of each species. The high and low dietary concentrations used in the chronic bioassay were 0.012 and 0.006 percent, respectively, for both species. After a 104-week period of chemical administration, observation of rats continued for up to 3 weeks and observation of mice continued for up to 1 week. For rats 50 animals of each sex were placed on test as controls, while for mice 55 animals of each sex were placed on test as controls. There were no significant positive associations between the dietary concentration of 2,3,5,6-tetrachloro-4-nitroanisole administered and mortality in rats or mice of either sex. Adequate numbers of animals in all groups survived sufficiently long to be at risk from late-developing tumors. No neoplasms, except for interstitial-cell testicular tumors in males, occurred at statistically significant incidences in dosed rats. Because of the high and variable spontaneous incidence of these lesions in Fischer 344 rats, these tumors were not considered to be associated with the administration of the test compound. Among dosed male mice the combined incidence of leukemia and malignant lymphoma was statistically significant. However, since these lesions were not spontaneously and with high variation in B6C3F1 mice, the lesions were not considered to be associated with the administration of the test compound. No neoplasms were of a statistically significant incidence in dosed female mice. Under the conditions of this bioassay, dietary administration of 2,3,5,6-tetrachloro-4-nitroanisole was not carcinogenic to male or female Fischer 344 rats or B6C3F1 mice of either sex.

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2,3,5,6-四氯-4-硝基苯甲醚可能致癌性的生物测定(CAS No. 2438-88-2)。
采用Fischer 344大鼠和B6C3F1小鼠进行了2,4,5,6-四氯-4-硝基苯甲醚可能致癌性的生物测定。将2,3,5,6-四氯-4-硝基苯甲醚以两种浓度中的任意一种加入饲料中,分别饲喂每一物种的雄性和雌性动物。在慢性生物试验中,两种物种的高、低饮食浓度分别为0.012%和0.006%。化学给药104周后,大鼠观察持续3周,小鼠观察持续1周。对于大鼠,每性别50只动物作为对照,而对于小鼠,每性别55只动物作为对照。饲粮中2,3,5,6-四氯-4-硝基苯甲醚的浓度与大鼠和小鼠的死亡率均无显著正相关。所有组中都有足够数量的动物存活了足够长的时间,从而有患晚期肿瘤的风险。除雄性间质细胞睾丸肿瘤外,在给药大鼠中没有发生统计学上显著的肿瘤发生率。由于Fischer 344大鼠中这些病变的自发发生率高且可变,因此不认为这些肿瘤与试验化合物的施用有关。在给药的雄性小鼠中,白血病和恶性淋巴瘤的联合发病率有统计学意义。然而,由于这些病变不是自发的,并且在B6C3F1小鼠中具有很高的变异,因此不认为这些病变与试验化合物的施用有关。在给药的雌性小鼠中没有统计学上显著的肿瘤发生率。在本实验条件下,2,3,5,6-四氯-4-硝基苯甲醚对雌雄Fischer 344大鼠或B6C3F1小鼠均无致癌性。
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