Bioassay of carbromal for possible carcinogenicity.

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Abstract

A bioassay for the possible carcinogenicity of carbromal was conducted using Fischer 344 rats and B6C3F1 mice. Carbromal was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species with the exception of 49 low dose male mice and high dose female mice. Twenty animals of each sex and species were placed on test as controls. The high and low dietary concentrations of carbromal were, respectively, 2,500 and 1,250 ppm for rats and 2,500 and 1,250 ppm for mice. The compound was administered for 103 weeks to rats and for 78 weeks to mice. The period of compound administration was followed by an observation period of 1 week for rats and 26 weeks for mice. There was no significant positive associations between the concentrations of carbromal 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. Slight dose-related mean body weight depression was observed for male rats and for females of both species and the mean body weight among dosed male mice was lower than that for controls, indicating that the concentrations of carbromal administered to the animals in this bioassay may have approximated the maximum tolerated concentrations. None of the statistical tests for any site in female rats or in mice of either sex indicated a significant positive association between compound administration and tumor incidence. There was a significant positive association between the concentrations administered and the incidences of adrenal pheochromocytomas in male rats; however, the Fisher exact comparisons were not significant. Under the conditions of this bioassay, dietary administration of carbromal was not carcinogenic in Fischer 344 rats or B6C3F1 mice.

可能致癌性的生物测定。
以Fischer 344大鼠和B6C3F1小鼠为实验对象,对其可能的致癌性进行了生物测定。除49只低剂量雄性小鼠和高剂量雌性小鼠外,在饲料中以两种浓度中的任何一种给药,每组50只雄性和50只雌性动物。各性别、各物种各20只作为对照进行试验。大鼠饮食中铬铬的高、低浓度分别为2500 ppm和1250 ppm,小鼠为2500 ppm和1250 ppm。大鼠服用该化合物103周,小鼠服用78周。复方给药期后,大鼠观察1周,小鼠观察26周。在给药的大鼠或小鼠中,无论性别,胭脂红浓度与死亡率之间没有显著的正相关。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。在雄性大鼠和雌性大鼠中观察到轻微的剂量相关的平均体重下降,并且在给药的雄性小鼠中平均体重低于对照组,这表明在该生物试验中给药的动物浓度可能接近最大耐受浓度。对雌性大鼠或雌雄小鼠的任何部位进行的统计检验均未显示复方用药与肿瘤发病率之间存在显著的正相关。给药浓度与雄性大鼠肾上腺嗜铬细胞瘤发生率呈显著正相关;然而,费雪精确比较并不显著。在此生物试验条件下,膳食给药对Fischer 344大鼠或B6C3F1小鼠没有致癌作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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