Quantitative Analysis of Microperfusion in Contrast-Induced Nephropathy Using Contrast-Enhanced Ultrasound: An Animal Study

Objective: To investigate imaging biomarkers of microperfusion in contrast-induced nephropathy (CIN) using contrast enhanced ultrasound (CEUS). Materials and Methods: The CIN model was fabricated by administering indomethacin (10 mg/kg), L-NAME (15 mg/kg), and iopamidol (10 mL/kg) to Sprague-Dawley rats. After 24 hours, CEUS was performed on CIN (n = 6) and control (n = 6) rats with sulphur hexafluoride microbubbles (SonoVue). From time-intensity curves obtained from the kidney arriving time (AT), acceleration time (AC), time to peak (TTP), and peak enhancement (PE) were measured and compared between the groups. After CEUS, the rats were sacrificed, and cell apoptosis markers were evaluated to confirm the development of CIN. Results: Among CEUS parameters, AT (7.8 +/- 1.6 vs. 4.2 +/- 0.5 s, p = 0.002), AC (4.7 +/- 1.4 vs. 2.0 +/- 0.4 s, p = 0.002), and TTP (12.5 +/- 2.9 vs. 6.2 +/- 0.6 s, p = 0.002) were significantly prolonged in the CIN group compared to controls. PE was significantly higher in the control group than in the CIN group (17.1 +/- 1.9 vs. 12.2 +/- 2.0 dB, p = 0.004). In kidney tissue, mRNA and protein levels of the apoptotic makers were significantly higher in the CIN group than in the control group (p = 0.003 and p = 0.002). Conclusion: CEUS parameters can be used as imaging biomarkers for microperfusion in CIN. In rats with CIN, AT, AC, and TTP were significantly prolonged, while PE was significantly lower compared to controls.

Automated summary

This study investigated imaging biomarkers of microperfusion in contrast-induced nephropathy using contrast enhanced ultrasound (CEUS). Results showed that in rats with CIN, parameters like AT, AC, and TTP were significantly prolonged, while PE was lower compared to controls. Levels of apoptotic markers were also significantly higher in the CIN group.