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作 者:陈隆典[1,2,3,4] 冯鲁中[1,2,3,4] 倪伟虹 黄钦田 张辰官
机构地区:[1]南京市鼓楼医院消化科 [2]南京医科大学药理学教研室 [3]南京医科大学生化教研室 [4]南京医科大学病理学教研室
出 处:《南京医科大学学报(自然科学版)》1998年第2期132-135,共4页Journal of Nanjing Medical University(Natural Sciences)
摘 要:为建立大鼠淤胆模型,并观察熊去氧胆酸(UDCA)对其的作用。将雌性大鼠分成4组:对照组每只灌胃0.5%羧甲基纤维素(CMC);模型组每只灌胃雌二醇(EE)及氯丙嗪(CPZ);大剂量UDCA组每日给EE及CPZ,同时灌胃UDCA60mg/kg;小剂量UDCA组则给UDCA30mg/kg。给药14天,分别于第7及14天处死5及10只,停药7天后处死剩余5只,宰杀时取血测肝功能,称空腹体重及肝重,并取鼠肝标本切片光镜检查。结果:给药1周后模型组与对照组在脏器系数与生化指标方面有显著差异,2周后差异明显加大,且与UDCA剂量相关。本实验以EE及CPZ制成的大鼠淤胆肝损模型可用于临床肝内淤胆性疾病的基础研究;UDCA使大鼠免受肝毒性药物的攻击。In order to establish the model of cholestatic rats and observe the effect of UDCA on the model, we divided the female rats at random into 4 groups. A, control, 0.5% CMC 1 ml/100 mg b.w/d orally; B, model, EE 5 mg/kg.b.w./d+CPZ 30 mg/kg.b.w./d orally; C, UDCA (60 mg/kg.b.w./d) treated the model rats orally; D, UDCA (30 mg/kg.b.w./d)treated the model rats. Discontinued all the drugs on day 14. On day 7 and day 14 killed 5 and 10 rats respectively, then on day 21 killed the rest. On the killing day, assay T Bili, ALT, ALP, γGT; Measure the body and liver weight,calculate the organ coefficient (OC); Take the liver sample for hsitological study. Results: significant difference observed between the control and the model on OC and biochemical assay on day 7 ( P <0.01); The two UDCA treated groups were different significantly with the model on OE and ALT on day 7 ( P <0.05); On day 14, the difference even more significant between the model and the two treated groups ( P <0.01), and it is related with the UDCA doses. On day 21, the difference still showed between the model and the other groups. Conclusion: Established cholestatic rats with EE and CPZ can be used for clinical intrahepatic cholestasis research; UDCA can protect rat liver from the attack of hepatic toxic drugs.
分 类 号:R575.630.5[医药卫生—消化系统]
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