118 First pass vasodilator-stress myocardial perfusion CMR in mice on a clinical whole-body 3 Tesla scanner: validation against microspheres. (16th May 2012)

• Record Type: Journal Article
• Authors: Jogiya, R; Makowski, M; Phinikaridou, A; Chiribiri, A; Zarinabad, N; Kozerke, S; Botnar, R; Nagel, E; Plein, S
• Is Part Of: Heart. Volume 98(2012)Supplement 1
• Page Start: A66
• Page End: A67
• Publication Date: 2012-05-16
• Subjects: Cardiac MRI -- myocardial perfusion imaging -- murine perfusion; Heart -- Diseases -- Treatment -- Periodicals; Cardiology -- Periodicals; 616.12
• DOI: 10.1136/heartjnl-2012-301877b.118
• Languages: English
• ISSNs: 1355-6037

Abstract

Abstract : Background: Animal models are important to develop our understanding of the pathophysiology of cardiovascular disease and for the development of new therapies. While coronary autoregulation maintains resting MBF constant over a wide range of pathological conditions, MBF reserve during hyperaemic stress is impaired in several common disease processes. First pass contrast-enhanced myocardial perfusion is the standard CMR method for the estimation of MBF and MBF reserve in man, but is challenging in rodents because of the constraints related to the high temporal and spatial resolution requirements. Aim: To evaluate first pass vasodilator stress myocardial perfusion CMR of the mouse heart against microspheres as the gold standard for regional organ flow. Methods: Five healthy 6-month old C57BL/6J mice were anaesthetized using 2% isoflurane. CMR imaging was performed on a clinical 3.0 Tesla scanner (Philips Healthcare, Best, the Netherlands) with a 23 mm single loop surface coil and a murine monitoring and ECG gating system (SA Instruments, NY, USA). Vasodilator stress was induced using a slow injection of dipyrimadole via a tail vein catheter. Stress perfusion data were acquired with an injection of gadolinium contrast (Gadobutrol 0.5 mmol/kg) 30 s later. The perfusion pulse sequence has been reported1, in summary, it used a saturation recovery gradient echo method with 10-fold k-space and time domain undersampling with constrained image reconstruction using temporal basis sets (k-t PCA) to achieve a spatial resolution of 0.2×0.2×1.5 mm 3 and an acquisition window of 43 ms. Following stress perfusion mice were recovered. One week later the mice underwent repeat anaesthesia and stress testing with LV injections of fluorescent microspheres at rest and at stress. Microsphere images were analysed using confocal microscopy. Results: Data were acquired successfully in all five mice. Mean heart rate increased from 480±27.4 bpm at rest to 503±41.5 bpm (p=0.08) during vasodilatation. Mean myocardial blood flow at rest by Fermi-function constrained deconvolution in control mice was 3.4±0.5 ml/g/min and increased to 8.9±3.0 ml/g/min during stress (ratio 2.6:1, p=0.036). The mean count of microspheres increased from rest to stress by a ratio of 2.7:1 (mean spheres per slice n=27±3.2, n=74±18.5, p=0.0005). Conclusion: First-pass myocardial stress perfusion CMR in a mouse model is feasible. Although the quantification of myocardial blood was lower than published values, the trend in myocardial blood flow was consistent with existing literature. Data were acquired on a 3 Tesla scanner using an approach similar to clinical acquisition protocols, thus facilitating translation of imaging findings between rodent and human studies to elucidate mechanisms and develop therapies for cardiovascular disease.