Berstein L M, Pozharisski K M, Dilman V M
Oncology. 1982;39(5):331-5. doi: 10.1159/000225663.
Intestinal tumors were induced by treatment with dimethylhydrazine (DMH) (14 mg with reference to base/kg body weight, weekly, s.c., for 20 weeks) in male rats supplied by Rappolovo Animal Farm. Some of the animals received 25 mg/day of misclerone (clofibrate) per os, 5 times a week. Clofibrate treatment did not affect the frequency of tumors of the large and small intestine but was followed by a significant decrease in the number of large- and medium-size tumors. The animals which had received clofibrate beginning from 10 days before the first injection of DMH revealed a relatively greater fraction of exophytic intestinal tumors and less invasion of the intestinal wall as compared with the animals treated with DMH alone. Possible mechanisms of the effect of clofibrate are discussed.
用二甲基肼(DMH)(14毫克碱基/千克体重,每周皮下注射,共20周)处理来自拉波洛沃动物农场的雄性大鼠,诱发肠道肿瘤。部分动物口服氯贝丁酯(安妥明),剂量为每天25毫克,每周5次。氯贝丁酯治疗不影响大肠和小肠肿瘤的发生率,但可使大、中尺寸肿瘤的数量显著减少。与仅接受DMH治疗的动物相比,从首次注射DMH前10天开始接受氯贝丁酯治疗的动物,其外生性肠道肿瘤的比例相对更高,肠壁侵犯更少。文中讨论了氯贝丁酯作用的可能机制。