Mouse model of ischemic acute kidney injury: technical notes and tricks
Author(s) -
Qingqing Wei,
Zheng Dong
Publication year - 2012
Publication title -
ajp renal physiology
Language(s) - English
Resource type - Journals
eISSN - 1931-857X
pISSN - 1522-1466
DOI - 10.1152/ajprenal.00352.2012
Subject(s) - acute kidney injury , medicine , ischemia , in vivo , genetically modified mouse , animal model , kidney , disease , renal ischemia , kidney disease , preclinical testing , intensive care medicine , transgene , cardiology , reperfusion injury , biology , gene , medical physics , microbiology and biotechnology , biochemistry
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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