ANIMAL MODEL OF ACUTE KIDNEY INJURY

SH Salim S. Hayek
DL David E. Leaf
AT Ayman Samman Tahhan
MR Mohamad Raad
SS Shreyak Sharma
SW Sushrut S. Waikar
SS Sanja Sever
AC Alex Camacho
XW Xuexiang Wang
RD Ranadheer R. Dande
NI Nasrien E. Ibrahim
RB Rebecca M. Baron
MA Mehmet M. Altintas
CW Changli Wei
DS David Sheikh-Hamad
JP Jenny S.-C. Pan
MJ Michael W. Holliday, Jr.
JJ James L. Januzzi
SW Steven D. Weisbord
AQ Arshed A. Quyyumi
JR Jochen Reiser
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We used C57BL/6J wild-type mice and transgenic mice overexpressing suPAR in an animal model of contrast-induced nephropathy to study the effect of suPAR on kidney function.12,17 The median suPAR level in the suPAR-transgenic mice at 10 weeks of age was 210 ng per milliliter (interquartile range, 160 to 256). We injected iohexol intraperitoneally in suPAR-transgenic mice (20 mice, 9 of which were male) and in wild-type controls (16 mice, 8 of which were male) following published protocols.31 The mice were also randomly assigned to receive an intraperitoneal injection of either urokinase plasminogen activator receptor (uPAR)–blocking monoclonal antibody or the same concentration of IgG isotype. Serum creatinine and kidney histologic tests were used to assess the severity of acute kidney injury. Experimental details are provided in the Supplementary Appendix.14,16,32,33 The study was approved by the Institutional Animal Care and Use Committee of Rush University in Chicago.

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