丙卡嗪可能致癌性的生物测定。

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引用次数: 0

摘要

通过对Sprague-Dawley大鼠和B6C3F1小鼠进行腹腔注射,对丙卡嗪的致癌性进行了生物测定。每组34或35只雄鼠和35或36只雌鼠按两种剂量中的一种给药,大鼠为15或30毫克/公斤,小鼠为6或12毫克/公斤。每周注射三次,大鼠注射26周,小鼠注射52周。注射期结束后,大鼠观察时间最长为60周,小鼠观察时间最长为33周,视存活率而定。用于统计评价的模型对照组,各性别10只大鼠和15只小鼠,按与试验溶液相同的时间给予生理盐水;同样数量的大鼠和小鼠作为未经治疗的对照组。混合对照包括本生物测定的载体对照以及在同一实验室进行的其他两种类似生物测定的载体对照。混合对照组由各性别40只大鼠和各性别45只小鼠组成。存活的大鼠在86周时被杀死,存活的小鼠在85周时被杀死。低、高剂量大鼠和高剂量雌性小鼠的平均体重均低于对照。大鼠和小鼠的存活率都显示出明显的剂量相关趋势。在大鼠中,诱导的恶性淋巴瘤、乳腺腺癌、嗅觉神经母细胞瘤、腺癌或脑癌、嗅球癌或脑癌的数量具有统计学意义。在小鼠中,诱导恶性淋巴瘤或白血病、嗅觉神经母细胞瘤或未分化癌、肺泡/细支气管腺瘤和子宫腺癌的数量具有统计学意义。由此可见,在本实验条件下,丙卡嗪对Sprague-Dawley大鼠和B6C3F1小鼠均具有致癌性,在这两种小鼠中均产生多种肿瘤。
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Bioassay of procarbazine for possible carcinogenicity.

A bioassay of procarbazine for possible carcinogenicity was conducted by administering the test chemical by intraperitoneal injection to Sprague-Dawley rats and B6C3F1 mice. Groups of 34 or 35 males and 35 or 36 females of both species were administered procarbazine at one of two doses, either 15 or 30 mg/kg for rats, and either 6 or 12 mg/kg for mice. Injections were made three times per week for 26 weeks for the rats and 52 weeks for the mice. Following the periods of injection, the dosed animals were observed for a maximum period of 60 weeks for rats and 33 weeks for mice, depending on survival. Vehicle controls, used for statistical evaluation, consisted of 10 rats and 15 mice of each sex, administered saline solution on the same schedule as the test solution; the same numbers of rats and mice served as untreated controls. Pooled controls consisted of the vehicle controls from this bioassay together with the vehicle controls from two other bioassays similarly performed at the same laboratory. The pooled-control groups consisted of 40 rats of each sex and 45 mice of each sex. Surviving rats were killed at 86 weeks and surviving mice were killed at 85 weeks. Mean body weights of low- and high-dose rats and of high-dose female mice were lower than those of the vehicle controls. Survival rates of both rats and mice showed significant dose-related trends. In rats, malignant lymphomas, adenocarcinomas of the mammary gland, and the combination of olfactory neuroblastomas, adenocarcinomas, or carcinomas of the brain, olfactory bulb, or cerebrum were induced in statistically significant numbers. In mice, malignant lymphomas or leukemias, olfactory neuroblastomas or undifferentiated carcinomas, alveolar/bronchiolar adenomas, and adenocarcinomas of the uterus were induced in statistically significant numbers. It is concluded that under the conditions of this bioassay, procarbazine was carcinogenic for both Sprague-Dawley rats and B6C3F1 mice, producing several types of tumors in both of these two species.

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