三甲基磷酸可能致癌性的生物测定。

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引用次数: 0

摘要

对Fischer 344大鼠和B6C3F1小鼠灌胃三甲基磷酸进行了可能致癌性的生物测定。每组各50只大鼠和50只小鼠,每周三次,以两种剂量中的一种给药,大鼠为50或100毫克/公斤体重,小鼠为250或500毫克/公斤体重。载体对照组由各性别20只大鼠和20只小鼠组成。大鼠给药104周,小鼠给药103周。105周处死所有存活的大鼠,103周处死所有存活的小鼠。在整个研究过程中,给药的雄性、雌性大鼠和雌性小鼠的平均体重略低于相应的载体对照;雄鼠的平均体重与对照组相当。大鼠和小鼠的存活率都很高,并且有足够数量的动物面临晚期肿瘤发展的风险。在雄性大鼠中,高剂量组皮下组织纤维瘤的发生率高于对照(对照组0/20,低剂量2/50,高剂量9/49)(P=0.036),且这些纤维瘤的发生率呈剂量相关趋势(P=0.006)。在雌性大鼠中,与相应的对照组相比,剂量组未发生肿瘤,但发生率显著增加。在雄性小鼠中,与对照组相比,服用剂量组没有发生肿瘤,但发病率明显增加。在雌性小鼠中,高剂量组子宫内膜腺癌的发生率高于对照组(对照组0/16,低剂量组7/40,高剂量组13/37)(P=0.004),且这些腺癌的发生率存在显著的剂量相关趋势(P=0.003)。由此可见,在本实验条件下,三甲基磷酸对雌性B6C3F1小鼠具有致癌性,可诱导子宫/子宫内膜腺癌。三甲基磷酸与雄性Fischer 344大鼠皮下组织良性纤维瘤的诱导有关。在雌性大鼠或雄性小鼠中没有发现该化合物致癌性的证据。
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Bioassay of trimethylphosphate for possible carcinogenicity.

A bioassay of trimethylphosphate for possible carcinogenicity was conducted by administering the compound by gavage to Fischer 344 rats and B6C3F1 mice. Groups of 50 rats and 50 mice of each sex were administered trimethylphosphate in distilled water three times per week at one of two doses, either 50 or 100 mg/kg body weight for the rats and either 250 or 500 mg/kg body weight for the mice. Vehicle controls consisted of groups of 20 rats and 20 mice of each sex. The rats were dosed for 104 weeks and the mice for 103 weeks. All surviving rats were killed at week 105 and all surviving mice at week 103. Mean body weights of dosed male and female rats and female mice were slightly lower than those of the corresponding vehicle controls throughout the study; mean body weights of the male mice were comparable to those of the vehicle controls. Survival rates of both rats and mice were high, and adequate numbers of animals were at risk for the development of late-appearing tumors. In male rats, the incidence of fibromas of the subcutaneous tissue was higher (P=0.036) in the high-dose group than in the vehicle controls (control 0/20, low-dose 2/50, high-dose 9/49), and there was a dose-related trend (P=0.006) in the incidences of these fibromas. In the female rats, no tumors occurred in the dosed groups at significantly increased incidences, compared with corresponding controls. In the male mice, no tumors occurred in the dosed groups at significantly increased incidences, compared with controls. In the female mice, the incidence of adenocarcinomas of the endometrium was higher (P=0.004) in the high-dose group than in the vehicle controls (controls 0/16, low-dose 7/40, high-dose 13/37), and there was a significant dose-related trend (P=0.003) in the incidences of these adenocarcinomas. It is concluded that under conditions of this bioassay, trimethylphosphate was carcinogenic in female B6C3F1 mice, inducing adenocarcinomas of the uterus/endometrium. Trimethylphosphate was associated with the induction of benign fibromas of the subcutaneous tissue in male Fischer 344 rats. No evidence of carcinogenicity of the compound was obtained in female rats or in male mice.

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