硫丹可能致癌性的生物测定。

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摘要

用奥斯本-孟德尔大鼠和B6C3F1小鼠进行了技术级硫丹可能致癌性的生物测定。以两种浓度中的任意一种,在饲料中添加硫丹,每组50只雄性和50只雌性动物。时间加权平均饮食中硫丹的高、低浓度分别为雄性大鼠952和408 ppm,雌性大鼠445和223 ppm。在小鼠中,高、低时间加权平均浓度雄性分别为6.9和3.5 ppm,雌性分别为3.9和2.0 ppm。各性别、各物种各20只作为对照进行试验。高剂量雄性大鼠的生物实验在第82周结束,低剂量雄性大鼠的生物实验在第74周结束。化学给药78周后,雌性大鼠再观察33周,小鼠再观察14周。在本研究中,给药剂量的大鼠硫丹是有毒的,在两性中引起高发生率的中毒性肾病和雄性睾丸萎缩。在这两个物种中,雄性组中观察到较高的早期死亡率,并且从这部分生物测定中无法得出关于硫丹致癌性的结论。然而,两种雌性的存活率足以对晚期肿瘤的发生率进行有意义的统计评估。在本实验条件下,技术级硫丹对雌性奥斯本-孟德尔大鼠和雌性B6C3F1小鼠均无致癌性。
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Bioassay of endosulfan for possible carcinogenicity.

A bioassay of technical-grade endosulfan for possible carcinogenicity was conducted using Osborne-Mendel rats and B6C3F1 mice. Endosulfan was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species. The time-weighted average high and low dietary concentrations of endosulfan were, respectively, 952 and 408 ppm for the male rats, and 445 and 223 ppm for the female rats. In mice the high and low time-weighted average concentrations were, respectively, 6.9 and 3.5 ppm for the males and 3.9 and 2.0 ppm for the females. Twenty animals of each sex and species were placed on test as controls. The bioassay of high dose male rats was terminated during week 82, and the bioassay of low dose male rats was terminated during week 74. After a 78-week period of chemical administration, observation of female rats continued for 33 additional weeks and observation of mice continued for 14 additional weeks. At the doses administered to rats in this study endosulfan was toxic, inducing a high incidence of toxic nephropathy in both sexes and testicular atrophy in males. In both species high early mortality was observed in the male groups and no conclusions concerning the carcinogenicity of endosulfan can be drawn from this part of the bioassay. However, survival among females of both species was sufficient for meaningful statistical evaluation of the incidence of late-developing tumors. It is concluded that under the conditions of this bioassay, technical-grade endosulfan was not carcinogenic in female Osborne-Mendel rats or in female B6C3F1 mice.

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