High-field magnetic resonance microscopy of aortic plaques in a mouse model of atherosclerosis

被引:5
|
作者
Castro, Rita [1 ,2 ]
Gullette, Sean [3 ]
Whalen, Courtney [1 ]
Mattie, Floyd J. [1 ]
Ge, Ximing [1 ]
Ross, A. Catharine [1 ]
Neuberger, Thomas [3 ,4 ]
机构
[1] Penn State Univ, Dept Nutr Sci, University Pk, PA 16802 USA
[2] Univ Lisbon, Fac Pharm, Lisbon, Portugal
[3] Penn State Univ, Huck Inst Life Sci, University Pk, PA 16802 USA
[4] Penn State Univ, Dept Biomed Engn, University Pk, PA 16802 USA
关键词
Atherosclerotic plaque; Ex-vivo MRI; MR microscopy; Plaque burden; HIGH-RESOLUTION MRI; IN-VIVO; APOE KNOCKOUT; MICE; QUANTIFICATION; LESIONS;
D O I
10.1007/s10334-023-01102-1
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
ObjectivesPre-clinical models of human atherosclerosis are extensively used; however, traditional histological methods do not allow for a holistic view of vascular lesions. We describe an ex-vivo, high-resolution MRI method that allows the 3 dimensional imaging of the vessel for aortic plaque visualization and quantification.Materials and methodsAortas from apolipoprotein-E-deficient (apoE(-/-)) mice fed an atherogenic diet (group 1) or a control diet (group 2) were subjected to 14 T MR imaging using a 3D gradient echo sequence. The obtained data sets were reconstructed (Matlab), segmented, and analyzed (Avizo). The aortas were further sectioned and subjected to traditional histological analysis (Oil-Red O and hematoxylin staining) for comparison.ResultsA resolution up to 15 x 10x10 & mu;m(3) revealed that plaque burden (mm(3)) was significantly (p < 0.05) higher in group 1 (0.41 & PLUSMN; 0.25, n = 4) than in group 2 (0.01 & PLUSMN; 0.01, n = 3). The achieved resolution provided similar detail on the plaque and the vessel wall morphology compared with histology. Digital image segmentation of the aorta's lumen, plaque, and wall offered three-dimensional visualizations of the entire, intact aortas.Discussion14 T MR microscopy provided histology-like details of pathologically relevant vascular lesions. This work may provide the path research needs to take to enable plaque characterization in clinical applications.
引用
收藏
页码:887 / 896
页数:10
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