Journal List > J Korean Soc Radiol > v.62(2) > 1086715

Baik, Ahn, Park, and Chung: Dynamic Contrast-Enhanced MR Imaging of Renal Ischemia-Reperfusion Injury

Abstract

Purpose

To evaluate the usefulness of magnetic resonance imaging (MRI) in a renal ischemia-reperfusion injury.

Materials and Methods

Twenty-four rabbits were randomly divided into four groups, including a sham operated group (n=3). Renal ischemia was induced for 30 minutes (group 1), 60 minutes (group 2) and 120 minutes (group 3). MR imaging was performed before ischemia as well as one hour, 24 hours, and 72 hours after reperfusion. A 99mTc-dimercaptosuccinic acid (DMSA) scintigraphy was performed before ischemia, as well as 24 hours and 72 hours after reperfusion. The signal-to-noise ratio (SNR) on the T2WI, time-relative signal intensity (%RSI) curve on dynamic enhanced images, and relative left renal uptake (%) on DMSA scan were obtained and compared to the histologic findings.

Results

The SNR of the cortex on the T2WI changed significantly over the course of the reperfusion time (p<0.001), but was not significantly different among the ischemia groups. The area under the time-%RSI curve gradually decreased from cortex to inner medulla before ischemia, which was reversed and gradually increased after reperfusion. The areas under the time-%RSI curve of outer and inner medulla were significantly different among the ischemia groups (p=0.04, p=0.008). The relative renal uptake (%) of left kidney decreased significantly over the reperfusion time (p=0.03), and was also significantly different among the ischemia groups (p=0.005). Tubular cell necrosis was observed in 16 rabbits (76.2%). The histologic grades of group 3 were higher than those of group 1 and group 2 (p=0.002). Even in rabbits without tubular cell necrosis, the areas under the time-%RSI curves of the cortex, outer, and inner medulla after a 72 hour reperfusion time were significantly lower than those before ischemia (p=0.007, p=0.005, p=0.004).

Conclusion

The results of this study suggest that dynamic enhanced MR imaging could be a useful tool for the evaluation of renal ischemia and reperfusion injury.

Figures and Tables

Fig. 1

SNR on T2-weighted image during renal ischemia. SNR of cortex (Cx), outer medulla (OM) and inner medulla (IM) are significantly decreased after clamping of renal artery. Changes of SNR over time are not significant.

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Fig. 2

SNR of renal cortex on T2-weighted image before and after reperfusion. SNR of renal cortex is significantly decreased over time (p=0.003) but the difference of SNR among groups is not significant (p=0.42).

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Fig. 3

Sequential dynamic MR Images of a left kidney of 30 minutes ischemia group. Before ischemia, a high signal intensity band (arrows), migrating from cortex to inner medulla, was well demonstrated (A). One hour after reperfusion, the movement of high SI band was delayed (B). MRI after 24 (C) and 72 hours (D) reperfusion showed improved flow of Gd-DTPA through medulla.

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Fig. 4

Sequential dynamic MR Images of a left kidney of one hour ischemia group. Before ischemia, a high signal intensity band (arrows), migrating from cortex to inner medulla along time, was demonstrated (A). This high SI band was disappeared and stagnation of Gd-DTPA was noted in the medulla after one and 24 hours reperfusion (B, C). 72 hours after reperfusion, the migrating high SI band was not seen but the stagnation of Gd-DTPA in medulla was improved (D).

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Fig. 5

Sequential dynamic MR Images of a left kidney of two hour ischemia group. Before the ischmia, a high signal intensity band (arrows) migrating from cortex to inner medulla was well demonstrated (A). After reperfusion, all layers of kidney are strongly and persistently enhanced, regardless of reperfusion time (B-D).

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Fig. 6

Area under the time-relative signal intensity (%RSI) curve of renal cortex (A), outer medulla (B) and inner medulla (C) after reperfusion. Areas under %RSI curve of all layers are significantly changed over time. Areas under the time-%RSI curve of outer and inner medulla of 2 hour ischemia group are significantly higher than those of 30 minute ischemia group (p=0.004, p<0.001).

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Fig. 7

Area under the time-relative signal intensity (%RSI) curve along layers from cortex to inner medulla. Before ischemia, the area under the curve is gradually decreased from cortex to medulla (A). one hour after reperfusion, the area under the curve is reversed; the area is gradually increased from cortex to medulla (B). This pattern is also seen at 24 hours after reperfusion (C). 72 hours after reperfusion (D), 30 minute and one hour ischemia groups show little difference in the area under the curve between cortex and medulla whereas two hour ischemia group shows again higher area under the curve of renal medulla than that of cortex.

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Fig. 8

Relative left renal uptake (%) of 99mTc DMSA before and after reperfusion of left renal artery. Relative left renal uptake is significantly decreased over time (p=0.03). The two hour ischemia group shows significantly lower uptake than 30 minute and one hour ischemia groups after reperfusion (p=0.005).

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Fig. 9

Histology of left renal cortex (H and E). No sign of necrosis in proximal convoluted tubules (A, ×400). Necrosis of several tubular cells in grade I necrosis (arrow in B, ×400). Necrosis of All cells in a tubule in grade II necrosis (C, ×400). Necrosis extending across the inner cortex in group III necrosis (D, ×200).

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Table 1

Patterns of Time-Relative Signal Intensity Curve at 72 hours After Reperfusion and Mean of Time-to-Peak in Rabbits with Cyclic Curve Patterns Before Ischemia and After Reperfusion

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Table 2

Correlation Between Pathologic Grading and Ischemia Group

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p=0.002, Kruskal-Wallis test, *PCT, proximal convoluted tubule.

Table 3

Mean Value of Parameters of MRI and 99mTc-DMSA Scintigraphy Before Ischemia and After 72 hour Reperfusion in Rabbits Without Tubular Cell Necrosis

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* Paired t-test

Table 4

Mean Value of Parameters of MRI and 99mTc-DMSA Scintigraphy Before Ischemia and After 72 hour Reperfusion in Rabbits with Tubular Cell Necrosis

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* Paired t-test

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