目的建立良好、快捷、稳定的小鼠原发性肝癌模型。方法将128只雄性KM小鼠随机均分为8组:正常组给予自由饮食;二乙基亚硝胺(DEN)水溶液组每天给予含DEN(16.5 mg/kg)的水溶液;高剂量DEN麻油组(7次/周、3次/周、1次/周),经口给予含DEN(16.5 mg/kg)的麻油溶液;而低剂量DEN麻油组、nano-DEN组、纳米载体组则分别每周经口给予含DEN(8.25 mg/kg)的麻油溶液和nano-DEN或同量的纳米载体。20周后,处死小鼠,取肝脏标本,固定后行HE染色。结果 (1)含DEN的各组小鼠均出现不同程度毛色枯燥、无光泽、行动迟缓、体重增长缓慢;(2)20周时,同DEN水溶液组,高剂量DEN麻油组小鼠均出现肿瘤,且其1次/周的小鼠死亡率较低;(3)Nano-DEN组小鼠无死亡,且其肝脏损伤的HE评分较低剂量DEN麻油组严重。结论 DEN溶于麻油的经口给药增加了小鼠服药的顺应性,长期低频率给药能大大降低造模过程中的死亡率。而DEN的纳米微乳制剂,能增强对肝脏的损伤程度。
Objective To develop an efficient,fast and stable establishment method of mouse model of hepatocellular carcinoma. Methods 128 healthy Kunming male mice were equally divided into eight groups: normal group supplied with routine drinking water and food; diethylnitrosamine( DEN)-water group received 16. 5 mg / kg DEN in drinking water every day; high-dose DEN-oil groups received orally 16. 5 mg / kg of DEN oil solution once,3 times and 7 times per week,respectively; low-dose DEN-oil group and nano-DEN group received orally 8. 25 mg / kg DEN in oil or in nano-vehicle every week,while nano-vehicle group received only an equal amount of nano-vehicle. After twenty weeks,all mice were sacrificed. The paraffin-embedded mouse liver specimens were examined by pathology using HE staining. Results( 1)The mice treated with DEN solution showed dry and dull hair,slow movement and slow weight-gain to a varying degree.( 2) At the twentieth week,both the DEN-water group and high-dose DEN-oil group showed tumors,and the mortality of high-dose DEN-oil group( once per week) was low.( 3) There was no death of mice in the nano-DEN group,and the pathological examination revealed more serious liver injury in the nano-DEN group than in the low-dose DEN-oil group( once per week). Conclusions Oral administration of DEN-oil improved the dietary compliance of mice,and the mortality can be reduced significantly by long-term low frequency DEN administration. Microemulsion preparation of DEN dissolved in oil may enhance the DEN-induced liver damage.