Diffusion Weighted Imaging And T2 Mapping Detect Inflammatory Response In The Renal Tissue During Ischemia Induced Acute Kidney Injury In Different Mouse Strains And Predict Renal Outcome

To characterize ischemia reperfusion injury (IRI)-induced acute kidney injury (AKI) in C57BL/6 (B6) and CD1-mice by longitudinal functional MRI-measurement of edema formation (T2-mapping) and inflammation (diffusion weighted imaging (DWI)). IRI was induced with unilateral right renal pedicle clamping for 35min. 7T-MRI was performed 1 and 14 days after surgery. DWI (7 b-values) and multiecho TSE sequences (7 TE) were acquired. Parameters were quantified in relation to the contralateral kidney on day 1 (dl). Renal MCP-1 and IL-6-levels were measured by qPCR and serum-CXCL13 by ELISA. Immunohistochemistry for fibronectin and collagen-4 was performed. T2-increase on dl was higher in the renal cortex (127 +/- 5% vs. 94 +/- 6%, p < 0.01) and the outer stripe of the outer medulla (141 +/- 9% vs. 111 +/- 9%, p < 0.05) in CD1, indicating tissue edema. Medullary diffusivity was more restricted in CD1 than B6 (dl: 73 +/- 3% vs. 90 +/- 2%, p < 0.01 and d14: 77 +/- 5% vs. 98 +/- 3%, p < 0.01). Renal MCP-1 and IL-6-expression as well as systemic CXCL13-release were pronounced in CD1 on dl after IRI. Renal fibrosis was detected in CD1 on d14. T2-increase and ADC-reduction on dl correlated with kidney volume loss on d14 (r = 0.7, p < 0.05; r = 0.6, p < 0.05) and could serve as predictive markers. T2-mapping and DWI evidenced higher susceptibility to ischemic AKI in CD1 compared to B6.