慢性肾衰竭小鼠模型的建立及生物学特征 |
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引用本文: | 薛澄,周晨辰,王冬梅,戴兵,梅长林. 慢性肾衰竭小鼠模型的建立及生物学特征[J]. 中国中西医结合肾病杂志, 2014, 0(2): 118-121,I0006 |
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作者姓名: | 薛澄 周晨辰 王冬梅 戴兵 梅长林 |
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作者单位: | [1] 第二军医大学附属长征医院肾内科,上海200003 [2] 武警总医院肾内科,北京100039 |
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基金项目: | 本课题为上海市浦江人才计划项目(N0.12PJ1403300) |
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摘 要: | 目的:通过制备小鼠慢性肾衰竭(CRF)模型,观察小鼠的生物学特征,有助于研究CRF的发病机制,预防终末期肾病的发生.方法:30只6-8周龄C57雄性小鼠适应性饲养1周后,5/6肾切除法(5/6 NX)切除模型组左肾上下极,1周后切除右肾,6周后处死.动态观察小鼠一般情况、血清常规和生化指标、测量体重和血压变化,检测肾脏组织病理学的变化.结果:与假手术组和正常对照组相比,模型组小鼠6周后出现体重减低、血清高尿素氮、高肌酐、高磷、贫血、血压升高和尿量增多(均P〈0.05).肾脏病理发现残肾单位代偿性肥大,系膜基质增生,胶原沉积增多.结论:5/6 NX是理想的CRF小鼠模型制作方法,CRF小鼠具有营养不良,高血压和钙磷代谢紊乱等特征.
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关 键 词: | 动物模型 慢性肾衰竭 慢性肾脏病 |
The Model of Chronic Renal Failure in Mouse and Its Biological Characteristics |
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Affiliation: | XUE Cheng, ZHOU Chenchen, WANG Dongmei, et al Department of Nephrology, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai (200003) |
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Abstract: | Objective:We produced the model of chronic renal failure (CRF) in mice which will help us study the patho genesis of CRF to prevent the occurrence of ESRD. Methods:30 C57 male mice (6 - 8 weeks' old) were adapted for 1 week. Then the model group underwent unilateral renal ablation by 5/6 nephrectomy (5/6 NX). The upper and low poles of the left kidney were cut. The right kidney was removed 1 week later. All the mice were executed at 6 weeks. The general conditions, serum biochemical parameters, measurement of body weight and blood pressure changes were observed. The detection of renal histopathological changes was also made. Results:Compared with the sham group and the normal control group, the model group lost weight, had higher serum urea nitrogen, creatinine, phosphorus, blood pressure, urine output and anemia (P 〈 0.05, respectively). The residual renal units of the model group got compensatory hypertrophy, proliferative mesangial matrix, and increased collagen deposition. Conclusion:The 5/6 NX was an appropriate way to produce the CRF model. CRF mice had many characteristics such as malnutrition, high blood pressure, calcium and phosphorus metabolism disorder and et al. |
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Keywords: | Animal model Chronic renal failure Chronic kidney disease |
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