Bioassay of 2,5-dithiobiurea for possible carcinogenicity.

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Abstract

A bioassay of 2,5-dithiobiurea for possible carcinogenicity was conducted using Fischer 344 rats and B6C3F1 mice. 2,5-Dithiobiurea 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 high dose male rats, of which there were only 49. The dietary concentrations used in the chronic bioassay were 0.6 percent for the low dose rats and 1.2 percent for the high dose rats. The dietary concentrations used for low and high dose mice were 1.0 and 2.0 percent, respectively. After a 78-week dosing period, observation of the mice continued for an additional 16 weeks. For each species, 50 animals of each sex were placed on test as controls. In both species, adequate numbers of animals in all groups survived sufficiently long to be at risk from late-developing tumors. Compound-related mean body weight depression was observed in mice but not in rats. No consistent pattern of clinical signs was observed in either species. No tumors occurred at a significantly higher incidence in dosed rats than in their controls. Among female mice, the Cochran-Armitage test indicated a significant positive association between the incidence of hepatocellular carcinoma and dietary concentrations of 2,5-dithiobiurea. According to results of the Fisher exact test, the incidence of hepatocellular carcinoma was significantly higher in the high dose female mouse group when compared to the corresponding control group but not when compared to the laboratory historical control data. No neoplasms occurred at a significantly higher incidence in dosed male mice than in their controls. Under the conditions of this bioassay, the evidence suggested, but was insufficient to establish the carcinogenicity of 2,5-dithiobiurea for female B6C3F1 mice. The compound was not carcinogenic to male B6C3F1 mice or to male or female Fischer 344 rats.

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2,5-二硫代比脲可能致癌性的生物测定。
采用Fischer 344大鼠和B6C3F1小鼠对2,5-二硫代比脲进行了可能致癌性的生物测定。2,5-二硫代比脲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,高剂量雄性大鼠除外,其中只有49只。慢性生物测定中使用的饮食浓度低剂量大鼠为0.6%,高剂量大鼠为1.2%。低剂量和高剂量小鼠的饮食浓度分别为1.0%和2.0%。在78周的给药期后,对小鼠的观察又持续了16周。每个物种各取50只雌雄动物作为对照进行试验。在这两个物种中,所有群体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。在小鼠中观察到化合物相关的平均体重下降,而在大鼠中没有。在两种动物中均未观察到一致的临床症状。在给药的大鼠中,肿瘤的发生率没有明显高于对照组。在雌性小鼠中,Cochran-Armitage试验显示肝细胞癌的发病率与饮食中2,5-二硫代比脲的浓度之间存在显著的正相关。Fisher精确检验结果显示,与相应的对照组相比,高剂量雌性小鼠组的肝细胞癌发病率显著升高,但与实验室历史对照数据相比则无显著升高。在给药的雄性小鼠中,肿瘤发生率没有明显高于对照组。在此生物测定条件下,证据提示,但不足以确定2,5-二硫代脲对雌性B6C3F1小鼠的致癌性。该化合物对雄性B6C3F1小鼠和雌雄Fischer 344大鼠均无致癌性。
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