Abstract

BackgroundDynamic first pass contrast-enhanced myocardial perfusion is the standard CMR method for the estimation of myocardial blood flow (MBF) and MBF reserve in man, but it is challenging in rodents because of the high temporal and spatial resolution requirements. Hyperemic first pass myocardial perfusion CMR during vasodilator stress in mice has not been reported.MethodsFive C57BL/6 J mice were scanned on a clinical 3.0 Tesla Achieva system (Philips Healthcare, Netherlands). Vasodilator stress was induced via a tail vein catheter with an injection of dipyridamole. Dynamic contrast-enhanced perfusion imaging (Gadobutrol 0.1 mmol/kg) was based on a saturation recovery spoiled gradient echo method with 10-fold k-space and time domain undersampling (k-t PCA). One week later the mice underwent repeat anaesthesia and LV injections of fluorescent microspheres at rest and at stress. Microspheres were analysed using confocal microscopy and fluorescence-activated cell sorting.ResultsMean MBF at rest measured by Fermi-function constrained deconvolution was 4.1 ± 0.5 ml/g/min and increased to 9.6 ± 2.5 ml/g/min during dipyridamole stress (P = 0.005). The myocardial perfusion reserve was 2.4 ± 0.54. The mean count ratio of stress to rest microspheres was 2.4 ± 0.51 using confocal microscopy and 2.6 ± 0.46 using fluorescence. There was good agreement between cardiovascular magnetic resonance CMR and microspheres with no significant difference (P = 0.84).ConclusionFirst-pass myocardial stress perfusion CMR in a mouse model is feasible at 3 Tesla. Rest and stress MBF values were consistent with existing literature and perfusion reserve correlated closely to microsphere analysis. Data were acquired on a 3 Tesla scanner using an approach similar to clinical acquisition protocols, potentially facilitating translation of imaging findings between rodent and human studies.

Highlights

  • Dynamic first pass contrast-enhanced myocardial perfusion is the standard cardiovascular magnetic resonance (CMR) method for the estimation of myocardial blood flow (MBF) and MBF reserve in man, but it is challenging in rodents because of the high temporal and spatial resolution requirements

  • All mice tolerated the scanning without complication and rest/stress first-pass myocardial perfusion imaging was successfully performed

  • This study has shown that dynamic contrast enhanced myocardial perfusion CMR during dipyridamole-stress in a murine model is feasible at 3 Tesla

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Summary

Introduction

Dynamic first pass contrast-enhanced myocardial perfusion is the standard CMR method for the estimation of myocardial blood flow (MBF) and MBF reserve in man, but it is challenging in rodents because of the high temporal and spatial resolution requirements. Dynamic contrast-enhanced myocardial perfusion imaging during vasodilator stress is the method of choice for the detection of ischemia with CMR. Data are usually interpreted by visual analysis, estimations of MBF and MBF reserve can be derived from the acquired data [11,12] Such quantitative analysis methods increase the objectivity of the analysis and allow monitoring of disease progression and assessment of treatment efficacy, which is an important consideration in developing translatable rodent models of cardiovascular disease. Hyperemic myocardial first pass stress perfusion CMR in mice has not been reported or validated against microspheres

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