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Am J Physiol Renal Physiol 293: F1408-F1412, 2007. First published July 18, 2007; doi:10.1152/ajprenal.00083.2007
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INNOVATIVE METHODOLOGY

Detection of early changes in renal function using 99mTc-MAG3 imaging in a murine model of ischemia-reperfusion injury

John Roberts,1 Bo Chen,1 Lisa M. Curtis,1,3 Anupam Agarwal,1 Paul W. Sanders,1,3 and Kurt R. Zinn2

1Department of Medicine, Nephrology Research and Training Center, 2Department of Radiology, Multimodality Imaging Laboratory, University of Alabama at Birmingham, and 3Department of Veterans Affairs, Birmingham, Alabama

Submitted 16 February 2007 ; accepted in final form 5 July 2007

Accurate determination of renal function in mice is a major impediment to the use of murine models in acute kidney injury. The purpose of this study was to determine whether early changes in renal function could be detected using dynamic gamma camera imaging in a mouse model of ischemia-reperfusion (I/R) injury. C57BL/6 mice (n = 5/group) underwent a right nephrectomy, followed by either 30 min of I/R injury or sham surgery of the remaining kidney. Dynamic renal studies (21 min, 10 s/frame) were conducted before surgery (baseline) and at 5, 24, and 48 h by injection of 99mTc-mercaptoacetyltriglycine (MAG3; ~1.0 mCi/mouse) via the tail vein. The percentage of injected dose (%ID) in the kidney was calculated for each 10-s interval after MAG3 injection, using standard region of interest analyses. A defect in renal function in I/R-treated mice was detected as early as 5 h after surgery compared with sham-treated mice, identified by the increased %ID (at peak) in the I/R-treated kidneys at 100 s (P < 0.01) that remained significantly higher than sham-treated mice for the duration of the scan until 600 s (P < 0.05). At 48 h, the renal scan demonstrated functional renal recovery of the I/R mice and was comparable to sham-treated mice. Our study shows that using dynamic imaging, renal dysfunction can be detected and quantified reliably as early as 5 h after I/R insult, allowing for evaluation of early treatment interventions.

acute kidney injury; nuclear imaging; mice models of acute renal failure



Address for reprint requests and other correspondence: A. Agarwal, Div. of Nephrology, ZRB 614, Univ. of Alabama at Birmingham, Birmingham, AL 35294 (e-mail: agarwal{at}uab.edu)




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L. M. Curtis, S. Chen, B. Chen, A. Agarwal, C. A. Klug, and P. W. Sanders
Contribution of intrarenal cells to cellular repair after acute kidney injury: subcapsular implantation technique
Am J Physiol Renal Physiol, July 1, 2008; 295(1): F310 - F314.
[Abstract] [Full Text] [PDF]




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