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单次尾静脉注射法阿霉素大鼠肾病模型的建立 被引量:25

Establishment of a rat model of nephrosis induced by single tail vein injection of doxorubicin
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摘要 目的建立阿霉素大鼠肾病模型,并观察模型的动态变化。方法 26只Wistar雄性大鼠随机分为模型组(13只)和空白组(13只),模型组单次尾静脉注射阿霉素6.2 mg/kg,空白组注射等容积生理盐水。检测连续10周12 h尿蛋白定量、终末血生化指标,光镜、电镜下观察各组大鼠肾脏病理改变。结果模型组12 h尿蛋白定量造模后1周与空白组差异有显著性(P<0.01),第5周达到高峰;血总蛋白、白蛋白均低于空白组,甘油三酯、胆固醇、血尿素氮均高于空白组(均P<0.05),血肌酐差异无显著性(P=0.64)。肾脏病理改变:第5周为微小病变型,第10周为局灶性节段性肾小球硬化。结论单次尾静脉注射6.2 mg/kg阿霉素,可以成功建立渐进性的大鼠肾病综合征模型。 Objective To establish a rat model of doxorubicin-induced nephrotic syndrome and observe its dynamic development. Methods Twenty-six male Wistar rats were randomly divided into model group and control group. The model group received a single tail vein injection of doxorubicin 6.2 mg/kg body weight. The control group was injected with isotonic saline. 12-hour urines were collected and checked for 12 weeks once a week. Finally the rats were sacrificed, the blood biochemical indexes were checked, and renal morphological changes were examined by light and electron micros- copy. Results The urinary protein excretion in the model group was significantly increased ( P 〈 0.01 ) at the 7th day and reached a peak at 5th week. The serum total protein and albumin were decreased, triglyceride, cholesterol and blood urea nitrogen were increased ( all P 〈 0. 05 ), while serum creatinine was not significantly changed ( P = 0. 64). Minimal change disease was developed at the 5th Week, and focal segmental glomerulosclerosis was observed at the 10th week. Conclusion A model of progressive nephritic syndrome in rats can be successfully established by a single tail vein injection of doxorubicin in a dose of 6.2 mg/kg body weight.
出处 《中国实验动物学报》 CAS CSCD 2013年第1期1-4,107,共4页 Acta Laboratorium Animalis Scientia Sinica
基金 国家自然科学基金项目(编号:81072754) 国家自然科学基金项目(编号:81072398) 山东省科技发展计划(编号:2009GG10002044)
关键词 阿霉素 肾病综合征 蛋白尿 大鼠 Doxorubicin Nephrotic syndrome Proteinuria Rat
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