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使用氧化铁增强磁共振成像早期识别主动脉瓣硬化

Early identification of aortic valve sclerosis using iron oxide enhanced MRI.

作者信息

Hamilton Amanda M, Rogers Kem A, Belisle Andre J L, Ronald John A, Rutt Brian K, Weissleder Ralph, Boughner Derek R

机构信息

Department of Anatomy, The University of Western Ontario, London, ON, Canada.

出版信息

J Magn Reson Imaging. 2010 Jan;31(1):110-6. doi: 10.1002/jmri.22008.


DOI:10.1002/jmri.22008
PMID:20027578
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5638659/
Abstract

PURPOSE: To test the ability of MION-47 enhanced MRI to identify tissue macrophage infiltration in a rabbit model of aortic valve sclerosis (AVS). MATERIALS AND METHODS: The aortic valves of control and cholesterol-fed New Zealand White rabbits were imaged in vivo pre- and 48 h post-intravenous administration of MION-47 using a 1.5 Tesla (T) MR clinical scanner and a CINE fSPGR sequence. MION-47 aortic valve cusps were imaged ex vivo on a 3.0T whole-body MR system with a custom gradient insert coil and a three-dimensional (3D) FIESTA sequence and compared with aortic valve cusps from control and cholesterol-fed contrast-free rabbits. Histopathological analysis was performed to determine the site of iron oxide uptake. RESULTS: MION-47 enhanced the visibility of both control and cholesterol-fed rabbit valves in in vivo images. Ex vivo image analysis confirmed the presence of significant signal voids in contrast-administered aortic valves. Signal voids were not observed in contrast-free valve cusps. In MION-47 administered rabbits, histopathological analysis revealed iron staining not only in fibrosal macrophages of cholesterol-fed valves but also in myofibroblasts from control and cholesterol-fed valves. CONCLUSION: Although iron oxide labeling of macrophage infiltration in AVS has the potential to detect the disease process early, a macrophage-specific iron compound rather than passive targeting may be required.

摘要

目的:在兔主动脉瓣硬化(AVS)模型中,测试超顺磁性氧化铁纳米颗粒-47(MION-47)增强磁共振成像(MRI)识别组织巨噬细胞浸润的能力。 材料与方法:使用1.5特斯拉(T)MR临床扫描仪和电影稳态自由梯度回波(CINE fSPGR)序列,对对照组和喂食胆固醇的新西兰白兔的主动脉瓣在静脉注射MION-47前及注射后48小时进行体内成像。将注射MION-47后的主动脉瓣尖在3.0T全身MR系统上,使用定制梯度插入线圈和三维(3D)快速成像稳态采集(FIESTA)序列进行离体成像,并与来自对照组和喂食胆固醇且未注射造影剂的兔子的主动脉瓣尖进行比较。进行组织病理学分析以确定氧化铁摄取的部位。 结果:MION-47增强了体内图像中对照组和喂食胆固醇的兔子瓣膜的可视性。离体图像分析证实,注射造影剂的主动脉瓣中存在明显的信号缺失。在未注射造影剂的瓣膜尖中未观察到信号缺失。在注射MION-47的兔子中,组织病理学分析显示,不仅在喂食胆固醇的瓣膜的纤维巨噬细胞中有铁染色,在对照组和喂食胆固醇的瓣膜的肌成纤维细胞中也有铁染色。 结论:尽管氧化铁标记AVS中的巨噬细胞浸润有潜力早期检测疾病进程,但可能需要一种巨噬细胞特异性铁化合物而非被动靶向。

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引用本文的文献

[1]
Magnetic resonance imaging diagnosis of metastatic lymph nodes in a rabbit model: efficacy of PJY10, a new ultrasmall superparamagnetic iron oxide agent, with monodisperse iron oxide core and multiple-interaction ligands.

PLoS One. 2014-9-12

[2]
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Int J Inflam. 2011

[3]
Calcific aortic valve stenosis: methods, models, and mechanisms.

Circ Res. 2011-5-27

本文引用的文献

[1]
Unbiased discovery of in vivo imaging probes through in vitro profiling of nanoparticle libraries.

Integr Biol (Camb). 2009-2-9

[2]
The in vivo diagnosis of early-stage aortic valve sclerosis using magnetic resonance imaging in a rabbit model.

J Magn Reson Imaging. 2009-4

[3]
Intensive lipid lowering with simvastatin and ezetimibe in aortic stenosis.

N Engl J Med. 2008-9-25

[4]
Noninvasive detection of macrophage-rich atherosclerotic plaque in hyperlipidemic rabbits using "positive contrast" magnetic resonance imaging.

J Am Coll Cardiol. 2008-8-5

[5]
Fractionated Feridex and positive contrast: in vivo MR imaging of atherosclerosis.

Magn Reson Med. 2008-4

[6]
Nanoparticle PET-CT imaging of macrophages in inflammatory atherosclerosis.

Circulation. 2008-1-22

[7]
Aortic stenosis: assessment of the patient at risk.

J Interv Cardiol. 2007-12

[8]
Magnetic resonance imaging of vulnerable atherosclerotic plaques: current imaging strategies and molecular imaging probes.

J Magn Reson Imaging. 2007-9

[9]
Localization to atherosclerotic plaque and biodistribution of biochemically derivatized superparamagnetic iron oxide nanoparticles (SPIONs) contrast particles for magnetic resonance imaging (MRI).

Biomed Microdevices. 2007-10

[10]
Rosuvastatin affecting aortic valve endothelium to slow the progression of aortic stenosis.

J Am Coll Cardiol. 2007-2-6

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