Bioassay of 6-nitrobenzimidazole for possible carcinogenicity (CAS No. 94-52-0).

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Abstract

A bioassay for possible carcinogenicity of 6-nitrobenzimidazole was conducted using Fischer 344 rats and B6C3F1 mice. 6-Nitrobenzimidazole was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species. The dietary concentrations used in the chronic bioassay were 0.5 and 0.12 percent for the high and low dose rats, respectively, and 0.24 and 0.12 percent for the high and low dose mice, respectively. After a 78-week period of compound administration, observation of the rats continued for up to an additional 29 weeks and observation of the mice continued for an additional 18 weeks. For each species and each dosed group, 49 or 50 animals of each sex were placed on test as controls. There were no significant positive associations between the administered dietary concentrations of 6-nitrobenzimidazole and mortality in either sex of rats or mice. In all groups adequate numbers of animals survived sufficiently long to be at risk from late-developing tumors. Among both male and female mice, the incidences of hepatocellular carcinomas in high dose groups were statistically significant relative to controls. Among rats of both sexes, nonneoplastic lesions of the eyes and of the Harderian glands appeared to be associated with administration of 6-nitrobenzimidazole. No neoplasms, however, were attributed to compound administration. Under the conditions of this bioassay, dietary administration of 6-nitrobenzimidazole was not carcinogenic to Fischer 344 rats; however, the compound was carcinogenic to B6C3F1 mice, causing hepatocellular carcinomas in both sexes.

6-硝基苯并咪唑可能致癌性的生物测定(CAS No. 94-52-0)。
采用Fischer 344大鼠和B6C3F1小鼠对6-硝基苯并咪唑的致癌性进行了生物测定。将6-硝基苯并咪唑以两种浓度中的任意一种添加到饲料中,每组50只雄性和50只雌性动物。在慢性生物测定中,高剂量和低剂量大鼠的饮食浓度分别为0.5%和0.12%,高剂量和低剂量小鼠的饮食浓度分别为0.24%和0.12%。在78周的复合给药期后,对大鼠的观察持续了29周,对小鼠的观察持续了18周。对于每个物种和每个剂量组,每个性别的49或50只动物作为对照进行试验。饲粮中6-硝基苯并咪唑的浓度与大鼠和小鼠的死亡率均无显著正相关。在所有组中,有足够数量的动物存活足够长的时间,从而有可能罹患晚期肿瘤。在雄性和雌性小鼠中,高剂量组的肝细胞癌发生率相对于对照组有统计学意义。在雌雄大鼠中,眼睛和哈德氏腺的非肿瘤性病变似乎与6-硝基苯并咪唑的施用有关。然而,没有肿瘤归因于复合给药。在本实验条件下,6-硝基苯并咪唑对Fischer 344大鼠无致癌性;然而,该化合物对B6C3F1小鼠具有致癌性,在两性中均可引起肝细胞癌。
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