二苯并对二恶英可能致癌性的生物测定。

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引用次数: 0

摘要

通过给奥斯本-孟德尔大鼠和B6C3F1小鼠喂食饲料,对二苯并-对二恶英(UDD)进行了可能致癌性的生物测定。每组35只大鼠,雌雄各一,以两种剂量(5000或10000 ppm)中的一种给药,持续110周。每组各50只雌雄老鼠,在87周或90周内服用相同的剂量。对照组由每性别35只未治疗的大鼠和每性别50只未治疗的小鼠组成。所有存活的雄性大鼠在110周龄时被杀死,所有存活的雄性小鼠在92至97周龄时被杀死,所有存活的雌性小鼠在91至93周龄时被杀死。给药的雌雄大鼠和小鼠的平均体重均低于相应的对照组;然而,服用药物的雄性小鼠体重增加的幅度相对较小。除雄性大鼠外,两组大鼠或小鼠在生物测定结束时的存活率都低于相应的对照组。在第90周,至少57%的大鼠和54%的小鼠仍然存活。由于给药动物的平均体重和存活率低于相应的对照组,并且肝毒性病变的发生率增加,因此给予大鼠和小鼠的10,000 ppm浓度被认为是最大耐受剂量。两种性别的大鼠或小鼠均未发生肿瘤,但剂量组的发生率明显高于相应的对照组。由此可见,在本实验条件下,UDD对奥斯本-孟德尔大鼠和B6C3F1小鼠无致癌性。
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Bioassay of dibenzo-p-dioxin for possible carcinogenicity.

A bioassay of dibenzo-p-dioxin (UDD) for possible carcinogenicity was conducted by administering the test chemical in feed to Osborne-Mendel rats and B6C3F1 mice. Groups of 35 rats of each sex were administered UDD at one of two doses, either 5,000 or 10,000 ppm, for 110 weeks. Groups of 50 mice of each sex were administered the same doses for 87 or 90 weeks. Controls consisted of groups of 35 untreated rats of each sex and 50 untreated mice of each sex. All surviving male rats were killed at 110 weeks, all surviving male mice at 92 to 97 weeks, and all surviving female mice at 91 to 93 weeks. Mean body weights of the dosed male and female rats and mice were lower than those of the corresponding controls; the depression in the amount of weight gained in the dosed male mice was, however, relatively slight. Except for the male rats, survival at the end of the bioassay was lower in the dosed groups of both rats or mice than in the corresponding control groups. At week 90, at least 57% of the rats and 54% of the mice were still alive. Because the mean body weights and survival rates of the dosed animals were lower than those of corresponding controls and because there was an increase in the incidence of hepatotoxic lesions, the 10,000-ppm concentration administered to the rats and mice is considered to be the maximum tolerated dose. No tumors were induced in rats or mice of either sex at incidences that were significantly higher in the dosed groups than in the corresponding control groups. It is concluded that under the conditions of this bioassay, UDD was not carcinogenic for Osborne-Mendel rats or B6C3F1 mice.

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