High-resolution MRI with cardiac and respiratory gating allows for accurate in vivo atherosclerotic plaque visualization in the murine aortic arch

被引:69
作者
Wiesmann, F
Szimtenings, M
Frydrychowicz, A
Illinger, R
Hunecke, A
Rommel, E
Neubauer, S
Haase, A
机构
[1] Med Univ Klin Wurzburg, D-97080 Wurzburg, Germany
[2] Univ Wurzburg, Inst Phys, D-8700 Wurzburg, Germany
[3] Univ Oxford, John Radcliffe Hosp, Dept Cardiovasc Med, Oxford OX1 2JD, England
关键词
atherosclerosis; mouse aorta; magnetic resonance imaging; genetic engineering;
D O I
10.1002/mrm.10500
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Genetically engineered mouse models provide enormous potential for investigation of the underlying mechanisms of atherosclerotic disease, but noninvasive imaging methods for analysis of atherosclerosis in mice are currently limited. This study aimed to demonstrate the feasibility of MRI to noninvasively visualize atherosclerotic plaques in the thoracic aorta in mice deficient in apolipoprotein-E, who develop atherosclerotic lesions similar to those observed in humans. To freeze motion, MR data acquisition was both ECG- and respiratory-gated. T-1-weighted MR images were acquired with TR/TE similar to1000/10 ms. Spatial image resolution was 49 x 98 x 300 mum(3). MRI revealed a detailed view of the lumen and the vessel wall of the entire thoracic aorta. Comparison of MRI with corresponding cross-sectional histopathology showed excellent agreement of aortic vessel wall area (r = 0.97). Hence, noninvasive MRI should allow new insights into the mechanisms involved in progression and regression of atherosclerotic disease. Magn Reson Med 50: 69-74, 2003. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:69 / 74
页数:6
相关论文
共 16 条
[1]   Genes and physiology: Molecular physiology in genetically engineered animals [J].
Chien, KR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (04) :901-909
[2]   Atherosclerotic lesions in genetically modified mice quantified in vivo by non-invasive high-resolution magnetic resonance microscopy [J].
Choudhury, RP ;
Aguinaldo, JG ;
Rong, JX ;
Kulak, JL ;
Kulak, AR ;
Reis, ED ;
Fallon, JT ;
Fuster, V ;
Fisher, EA ;
Fayad, ZA .
ATHEROSCLEROSIS, 2002, 162 (02) :315-321
[3]  
Faraci FM, 1999, CIRC RES, V85, P1214
[4]   Noninvasive in vivo high-resolution magnetic resonance imaging of atherosclerotic lesions in genetically engineered mice [J].
Fayad, ZA ;
Fallon, JT ;
Shinnar, M ;
Wehrli, S ;
Dansky, HM ;
Poon, M ;
Badimon, JJ ;
Charlton, SA ;
Fisher, EA ;
Breslow, JL ;
Fuster, V .
CIRCULATION, 1998, 98 (15) :1541-1547
[5]   Repeated three-dimensional magnetic resonance imaging of atherosclerosis development in innominate arteries of low-density lipoprotein receptor-knockout mice [J].
Hockings, PD ;
Roberts, T ;
Galloway, GJ ;
Reid, DG ;
Harris, DA ;
Vidgeon-Hart, M ;
Groot, PHE ;
Suckling, KE ;
Benson, M .
CIRCULATION, 2002, 106 (13) :1716-1721
[6]   IN-VIVO ECHOCARDIOGRAPHIC DETECTION OF ENHANCED LEFT-VENTRICULAR FUNCTION IN GENE-TARGETED MICE WITH PHOSPHOLAMBAN DEFICIENCY [J].
HOIT, BD ;
HOURY, SF ;
KRANIAS, EG ;
BALL, N ;
WALSH, RA .
CIRCULATION RESEARCH, 1995, 77 (03) :632-637
[7]   Dilated cardiomyopathy in transgenic mice with cardiac-specific overexpression of tumor necrosis factor-alpha [J].
Kubota, T ;
McTiernan, CF ;
Frye, CS ;
Slawson, SE ;
Lemster, BH ;
Koretsky, AP ;
Demetris, AJ ;
Feldman, AM .
CIRCULATION RESEARCH, 1997, 81 (04) :627-635
[8]  
Manka DR, 2000, J MAGN RESON IMAGING, V12, P790, DOI 10.1002/1522-2586(200011)12:5<790::AID-JMRI19>3.0.CO
[9]  
2-6
[10]   IN-VIVO ASSESSMENT OF LV MASS IN MICE USING HIGH-FREQUENCY CARDIAC ULTRASOUND - NECROPSY VALIDATION [J].
MANNING, WJ ;
WEI, JY ;
KATZ, SE ;
LITWIN, SE ;
DOUGLAS, PS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (04) :H1672-H1675