可能致癌性的氰酰胺钙生物测定。

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引用次数: 0

摘要

通过给F344大鼠和B6C3F1小鼠喂食饲料中的试验化学品,对配制的氰酰胺钙进行了可能致癌性的生物测定。每组50只,雌雄各别,喂食含有63%氰胺钙的商业配方,两种剂量中的一种,雄性剂量为100或200 ppm,雌性剂量为100或400 ppm,持续107周。每组50只雌雄老鼠分别以两种剂量(500ppm或2000ppm)中的一种给药,持续100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。剂量大鼠和小鼠的平均体重仅略低于相应的对照组,但低剂量雌性小鼠的平均体重不受试验化学品的影响。死亡率仅在雄性小鼠中与剂量有关。在生物测定结束时,每个物种和性别的所有给药组和对照组的存活率为70%或更高,并且所有组中有足够数量的动物处于晚期肿瘤发展的风险中。大鼠和小鼠可能都能承受更高的剂量。在给药的大鼠中,无论性别,都没有肿瘤发生,其发生率显然与氰酰胺钙的施用有关。然而,在对大鼠进行的亚慢性研究中,发现氰酰胺钙引起甲状腺弥漫性滤泡增生,伴有腺周纤维化和突出的腺周血管。雄性小鼠血管肉瘤与剂量相关(P=0.006);然而,在直接比较中,个别给药组的发病率并不显著高于对照组(对照1/20 (5%);低剂量2/50 (4%);高剂量10/50(20%))。这些肿瘤在历史对照雄性B6C3F1小鼠中的发病率为(13/323(4%)),最高发病率为2/19(10%)。在雌性小鼠中,淋巴瘤或白血病与剂量相关(P=0.009),在直接比较中,高剂量组这些肿瘤的发生率显著高于对照组(对照1/20 (5%);低剂量11/46 (24%);高剂量18/50 (36%);然而,在历史对照组雌性B6C3F1小鼠中,淋巴瘤或白血病的发病率为67/324(21%),这表明在当前生物测定的匹配对照组中,这些肿瘤的发病率可能异常低。因此,无论是雄性小鼠的循环系统血管肉瘤的发生率,还是雌性小鼠的淋巴瘤或白血病的发生率,都不能明确地与试验化学品的施用有关。在本实验条件下,氰酰胺钙试验制剂对F344大鼠和B6C3F1小鼠均无致癌性。
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Bioassay of calcium cyanamide for possible carcinogenicity.

A bioassay of formulated calcium cyanamide for possible carcinogenicity was conducted by administering the test chemical in feed to F344 rats and B6C3F1 mice. Groups of 50 rats of each sex were administered a commercial formulation containing 63% calcium cyanamide in the diet at one of two doses, either 100 or 200 ppm for the males and either 100 or 400 ppm for the females, for 107 weeks. Groups of 50 mice of each sex were administered the test chemical at one of two doses, either 500 or 2,000 ppm, for 100 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 only slightly lower than those of corresponding controls, except for the low-dose female mice, whose mean body weights were unaffected by the test chemical. Mortality was dose related only in male mice. Survival was 70% or greater in all dosed and control groups of each species and sex at the end of the bioassay, and sufficient numbers of animals were at risk in all groups for the development of late-appearing tumors. Both rats and mice may have been able to tolerate higher doses. No tumors occurred in the dosed rats of either sex at incidences that could clearly be related to administration of the calcium cyanamide. However, in the subchronic studies performed with the rats, calcium cyanamide was found to cause diffuse follicular hyperplasia of the thyroid, with periglandular fibrosis and prominent periglandular vascularity. In male mice, hemangiosarcomas were dose related in the males (P=0.006); however, in direct comparisons, incidences in the individual dosed groups were not significantly higher than those in the control group (controls 1/20 (5%); low-dose 2/50 (4%); high-dose 10/50 (20%)). The incidence of these tumors in historical-control male B6C3F1 mice was (13/323 (4%)), and the highest incidence observed was 2/19 (10%). In female mice, lymphomas or leukemias were dose related (P=0.009), and in a direct comparison the incidence of these tumors in the high-dose group was significantly higher (P=0.006) than that in the control group (controls 1/20 (5%); low-dose 11/46 (24%); high-dose 18/50 (36%)); however, the incidence of the lymphomas or leukemias in historical-control female B6C3F1 mice was 67/324 (21%), suggesting that the incidence of these tumors in the matched-control group of the present bioassay may have been abnormally low. Thus, neither the incidences of hemangiosarcomas of the circulatory system in male mice nor of lymphomas or leukemias in the female mice can clearly be related to administration of the test chemical. It is concluded that under the conditions of this bioassay, the test formulation of calcium cyanamide was not carcinogenic for F344 rats or B6C3F1 mice of either sex.

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