急性肾损伤
医学
缺血
体内
动物模型
转基因小鼠
肾
肾缺血
疾病
肾脏疾病
临床前试验
重症监护医学
转基因
心脏病学
内科学
再灌注损伤
生物
基因
医学物理学
生物技术
生物化学
作者
Qingqing Wei,Zheng Dong
出处
期刊:American Journal of Physiology-renal Physiology
[American Physiological Society]
日期:2012-09-19
卷期号:303 (11): F1487-F1494
被引量:265
标识
DOI:10.1152/ajprenal.00352.2012
摘要
Renal ischemia-reperfusion leads to acute kidney injury (AKI), a major kidney disease associated with an increasing prevalence and high mortality rates. A variety of experimental models, both in vitro and in vivo, have been used to study the pathogenic mechanisms of ischemic AKI and to test renoprotective strategies. Among them, the mouse model of renal clamping is popular, mainly due to the availability of transgenic models and the relatively small animal size for drug testing. However, the mouse model is generally less stable, resulting in notable variations in results. Here, we describe a detailed protocol of the mouse model of bilateral renal ischemia-reperfusion. We share the lessons and experiences gained from our laboratory in the past decade. We further discuss the technical issues that account for the variability of this model and offer relevant solutions, which may help other investigators to establish a well-controlled, reliable animal model of ischemic AKI.
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