n -亚硝基二苯胺可能致癌性的生物测定。

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Because of excessive depression in the amount of mean body weight gained in the dosed groups, the doses for the females were then reduced to 1,000 and 4,000 ppm, respectively, and administration at the lowered doses was continued for 60 weeks. The time-weighted average doses for the female mice were either 2,315 or 5,741 ppm. Matched controls consisted of 20 untreated mice of each sex. All surviving mice were killed at the end of administration of the test chemical. Mean body weights of dosed rats and mice of each sex were lower than those of corresponding controls, and were dose related throughout the bioassay, except for those of female rats during the first part of the bioassay. Mortality was dose related in the female rats, but was not affected when the test chemical was administered to the male rats or the male or female mice. Survival at the end of the bioassay was 64% or greater in the dosed and control groups of rats and mice of each sex, and sufficient numbers of animals were at risk in all groups for the development of late-appearing tumors. Transitional-cell carcinomas of the urinary bladder occurred at incidences that were dose related (P</= 0.001) in both male and female rats, and in direct comparisons the incidences of these tumors in the high-dose groups of each sex were significantly higher (P</= 0.001) than those in the corresponding controls (males: controls 0/19; low-dose 0/46; high-dose 16/45; females: controls 0/18; low-dose 0/48; high-dose 40/49). The possible mechanism by which these tumors were induced, such as calculi formation in the bladder or nitrosation of amines present in feed to a carcinogenic nitrosoamine, is unknown. Fibromas of the integumentary system occurred in male rats at incidences that were dose related (P=0.003), although in direct comparisons the incidences of these tumors in the individual dosed groups were not significantly higher than those in the control group (controls 1/20, or 5%; low-dose 1/50, or 2%; high-dose 10/50, or 20%). The incidence of fibromas of the integumentary system in historical-control male F344 rats at this laboratory is 6/285, or 2%. These results suggest an association of the fibromas in the male rats with the administration of the test chemical. No tumors occurred in the mice of either sex at incidences that were significantly higher in the dosed groups than in the corresponding control groups. The only changes related to compound administration were chronic inflammatory lesions in the urinary bladders of dosed mice. 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引用次数: 0

摘要

对F344大鼠和B6C3F1小鼠进行了n -亚硝基二苯胺致癌性的生物测定。每组50只老鼠,每只雌雄,被注射两种剂量的n -亚硝基二苯胺,浓度分别为1000ppm或4000ppm,持续100周。配对的对照组包括20只未治疗的大鼠,雌雄各一只。在给药结束时,所有幸存的老鼠都被杀死。每组50只雄性老鼠被注射了两种剂量的n -亚硝基二苯胺,浓度分别为1万或2万ppm,持续101周。每组50只雌性老鼠被注射两种剂量中的一种,最初是5000或10000 ppm,持续38周。由于给药组的平均体重增加量过度下降,雌性的剂量分别减少到1,000 ppm和4,000 ppm,并以降低的剂量持续给药60周。雌性小鼠的时间加权平均剂量为2,315或5,741 ppm。配对的对照组由雌雄各20只未经治疗的老鼠组成。在给药结束时,所有幸存的老鼠都被杀死。各组大鼠和小鼠的平均体重均低于相应的对照组,且在整个生物测定过程中均与剂量相关,雌性大鼠在生物测定的第一部分除外。雌性大鼠的死亡率与剂量有关,但雄性大鼠或雄性或雌性小鼠服用试验化学品时,死亡率不受影响。在给药组和对照组中,各性别大鼠和小鼠在生物测定结束时的存活率为64%或更高,并且所有组中都有足够数量的动物处于晚期肿瘤发展的风险中。膀胱移行细胞癌的发生率与剂量有关(P
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Bioassay of N-nitrosodiphenylamine for possible carcinogenicity.

A bioassay of N-nitrosodiphenylamine 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 N-nitrosodiphenylamine at one of two doses, either 1,000 or 4,000 ppm, for 100 weeks. Matched controls consisted of 20 untreated rats of each sex. All surviving rats were killed at the end of administration of the test chemical. Groups of 50 male mice were administered N-nitrosodiphenylamine at one of two doses, either 10,000 or 20,000 ppm, for 101 weeks. Groups of 50 female mice were administered the test chemical at one of two doses, initially 5,000 or 10,000 ppm, for 38 weeks. Because of excessive depression in the amount of mean body weight gained in the dosed groups, the doses for the females were then reduced to 1,000 and 4,000 ppm, respectively, and administration at the lowered doses was continued for 60 weeks. The time-weighted average doses for the female mice were either 2,315 or 5,741 ppm. Matched controls consisted of 20 untreated mice of each sex. All surviving mice were killed at the end of administration of the test chemical. Mean body weights of dosed rats and mice of each sex were lower than those of corresponding controls, and were dose related throughout the bioassay, except for those of female rats during the first part of the bioassay. Mortality was dose related in the female rats, but was not affected when the test chemical was administered to the male rats or the male or female mice. Survival at the end of the bioassay was 64% or greater in the dosed and control groups of rats and mice of each sex, and sufficient numbers of animals were at risk in all groups for the development of late-appearing tumors. Transitional-cell carcinomas of the urinary bladder occurred at incidences that were dose related (P

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Bioassay of sulfisoxazole for possible carcinogenicity. Bioassay of diazinon for possible carcinogenicity. Bioassay of aldicarb for possible carcinogenicity. Bioassay of malaoxon for possible carcinogenicity. Bioassay of C.I. vat yellow 4 for possible carcinogenicity.
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