Abstract

Summary We used first-pass contrast-enhanced MRI to quantatively measure the myocardial Ktrans, a parameter indicating myocardial perfusion and vascular permeability, in mice with or without vasodilation. We measured a significant increase in myocardial Ktrans with vasodilation. We believe this may be the first report showing that first-pass imaging can quantify increased myocardial perfusion in mice relative to baseline. Background First-pass contrast-enhanced MRI is a well-established technique for quantifying myocardial perfusion in humans and large animals and has recently emerged as a viable tool for quantifying myocardial perfusion in mice [1-3]. Applied in mice, first-pass MRI could be used to assess the roles of individual genes in perfusion and vascular permeability. The purpose of this study was test the hypothesis that first-pass contrast-enhanced MRI can measure increased myocardial perfusion after administration of a vasodilator in mice. Methods Imaging was performed on a 7T Clinscan MR system equipped with a gradient system having a full strength of 650mT/m and as lew rate of 6666 mT/m/ms, and using a 30mm diameter birdcage RF coil. A saturationrecovery spiral sequence was employed, with TE = 0.36 ms, TR = 3.9ms, interleaves = 14, FOV = 25.6 x 25.6mm, matrix = 128x128, saturation delay = 40 ms, alpha = 20°, and slice thickness = 1mm. Data acquisition required 55 ms/image, approximately 40% of the murine R-R interval, and was placed in the latter part of the cardiac cycle. C57Bl6/J mice were imaged with (n=5) and without (n=5) an intraperitoneal bolus injection of the vasodilator ATL313 (Adenosine Therapeutics, Charlottesville, VA). First-pass images were acquired for one mid-ventricular short-axis slice. A dual-bolus gadolinium injection technique was used, acquiring the arterial input and tissue functions (AIF and TF) in separate scans. Myocardial Ktrans, the product of myocardial perfusion and the first-pass extraction fraction of gadolinium, was quantified using a standard Kety model deconvolution method. Results

Highlights

  • First-pass contrast-enhanced MRI is a well-established technique for quantifying myocardial perfusion in humans and large animals and has recently emerged as a viable tool for quantifying myocardial perfusion in mice [1,2,3]

  • Imaging was performed on a 7T Clinscan MR system equipped with a gradient system having a full strength of 650mT/m and a slew rate of 6666 mT/m/ms, and using a 30mm diameter birdcage RF coil

  • Example Gd concentration vs. time curves for the TF and AIF are shown in Figure 1, comparing mice with and without ATL313 vasodilation

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Summary

Background

First-pass contrast-enhanced MRI is a well-established technique for quantifying myocardial perfusion in humans and large animals and has recently emerged as a viable tool for quantifying myocardial perfusion in mice [1,2,3]. First-pass MRI could be used to assess the roles of individual genes in perfusion and vascular permeability. The purpose of this study was test the hypothesis that first-pass contrast-enhanced MRI can measure increased myocardial perfusion after administration of a vasodilator in mice

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