丁基羟基甲苯(BHT)可能致癌性的生物测定。

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引用次数: 0

摘要

通过给F344大鼠和B6C3F1小鼠喂食饲料,对BHT可能的致癌性进行了生物测定。每组各50只大鼠和50只小鼠被注射了两种剂量中的一种,即3000或6000 ppm;大鼠105周,小鼠107或108周。配对的对照组包括20只未治疗的大鼠和20只未治疗的小鼠。所有幸存的动物都在施用试验化学品结束时被杀死。给药的大鼠和小鼠的平均体重低于相应的对照组,并且在大部分生物测定中都与剂量相关。在给药组的大鼠或小鼠中,存活率没有受到显著影响,在生物测定结束时,所有给药组或对照组的大鼠和小鼠的存活率均为60%或更高。有足够数量的动物有发展为晚期肿瘤的风险。低剂量组雌性小鼠肺泡/细支气管癌或腺瘤发生率显著(P=0.009),高剂量组发生率不显著,且与剂量无关(对照组1/20,低剂量组16/46,高剂量组7/50)。因此,这些女性肺部肿瘤不能明确地与给予BHT有关。雄性或雌性大鼠均未发生肿瘤,剂量组的发生率明显高于相应的对照组。非肿瘤性病变可能与试验化学物质的施用有关,包括局灶性肺泡组织细胞增生,在给药的雌性大鼠中发病率增加,在给药的雄性小鼠中肝脏的各种病变发病率增加。本实验条件下,BHT对F344大鼠和B6C3F1小鼠均无致癌性。
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Bioassay of butylated hydroxytoluene (BHT) for possible carcinogenicity.

A bioassay of BHT for possible carcinogenicity was conducted by administering the test chemical in feed to F344 rats and B6C3F1 mice. Groups of 50 rats and 50 mice of each sex were administered BHT at one of two doses, either 3,000 or 6,000 ppm; the rats for 105 weeks and the mice for 107 or 108 weeks. Matched controls consisted of 20 untreated rats and 20 untreated mice of each sex. All surviving animals were killed at the end of administration of the test chemical. Mean body weights of the dosed rats and mice were lower than those of the corresponding controls and were dose related throughout most of the bioassay. Survival was not affected significantly in the dosed groups of rats or mice, and the survival was 60% or greater in all dosed or control groups of rats and mice of each sex at the end of the bioassay. Sufficient number of animals were at risk for the development of late-appearing tumors. Alveolar/bronchiolar carcinomas or adenomas occurred in the female mice at a significant incidence in the low-dose group (P=0.009) but not in the high dose group, and the incidences were not significantly dose related (control 1/20, low-dose 16/46, high-dose 7/50). Thus, these lung tumors in the female cannot clearly be related to the administration of the BHT. No tumors occurred in either male or female rats at incidences that were significantly higher in dosed groups than in corresponding control groups. Nonneoplastic lesions that may have been related to the administration of the test chemical included focal alveolar histiocytosis at increased incidences in the dosed female rats and various lesions of the liver at increased incidences in the dosed male mice. It is concluded that under the conditions of this bioassay, BHT was not carcinogenic for F344 rats or B6C3F1 mice.

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