盐酸对茴香胺可能致癌性的生物测定(CAS No. 20265-97-8)。

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引用次数: 0

摘要

采用Fischer 344大鼠和B6C3F1小鼠对盐酸茴香胺进行了可能致癌性的生物测定。将对茴香胺盐酸盐以两种浓度中的任意一种添加到饲料中,每组55只雄性和55只雌性动物。各性别、各物种的55只动物作为对照进行试验。大鼠饲粮中对茴香胺的高、低浓度分别为0.6%和0.3%,小鼠饲粮中对茴香胺的高、低浓度分别为1.0%和0.5%。给药103周,大鼠观察2 ~ 3周,小鼠观察2周。对茴香胺浓度与死亡率之间没有显著的正相关关系。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。在雄性大鼠中,复方给药与皮肤鳞状细胞癌和肺泡/细支气管腺瘤的发病率之间存在显著关联。然而,费舍尔精确的比较都没有支持这些发现。当将患有NOS腺瘤或包皮腺癌的男性合并并对其发病率进行统计分析时,唯一提供显著结果的测试是低剂量与对照组的Fisher精确比较。在任何性别的小鼠中,对茴香胺盐酸盐的施用与任何肿瘤的发生率之间没有显著的正相关。虽然,在这种生物测定条件下,在低剂量雄性大鼠中,化学给药与包膜腺肿瘤发生率增加之间似乎存在关联,但证据不足以确定对茴香胺盐酸盐在Fischer 344大鼠中的致癌性。该化合物对B6C3F1小鼠无致癌性。
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Bioassay of p-Anisidine Hydrochloride for Possible Carcinogenicity (CAS No. 20265-97-8).

A bioassay for possible carcinogenicity of p-anisidine hydrochloride was conducted using Fischer 344 rats and B6C3F1 mice. p-Anisidine hydrochloride was administered in the feed, at either of two concentrations, to groups of 55 male and 55 female animals of each species. Fifty-five animals of each sex and species were placed on test as controls. The high and low dietary concentrations of p-anisidine hydrochloride were, respectively, 0.6 and 0.3 percent for rats and 1.0 and 0.5 percent for mice. The compound was administered in the diet for 103 weeks, followed by an observation period of 2 to 3 weeks for rats and 2 weeks for mice. There were no significant positive associations for either species between the concentration of p-anisidine hydrochloride administered and mortality. In addition, adequate numbers of animals in all groups survived sufficiently long to be at risk from late-developing tumors. In male rats there were significant associations between compound administration and the incidences of both squamous-cell carcinomas of the skin and alveolar/bronchiolar adenomas. None of the Fischer exact comparisons, however, supported these findings. When those males having adenomas NOS or carcinomas NOS of the preputial gland were combined and the resulting incidences statistically analyzed, the only test providing a significant result was the Fisher exact comparison of the low dose to the control. There were no significant positive associations between the administration of p-anisidine hydrochloride and the incidence of any tumor in mice of either sex. Although, under the conditions of this bioassay, there appeared to be an association between chemical administration and the increased incidence of preputial gland tumors in low dose male rats, the evidence was insufficient to establish the carcinogenicity of p-anisidine hydrochloride in Fischer 344 rats. The compound was not carcinogenic in B6C3F1 mice.

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