In Vivo Evaluation of a New Magnetic Resonance Imaging Contrast Agent (P947) to Target Matrix Metalloproteinases in Expanding Experimental Abdominal Aortic Aneurysms

被引:35
作者
Bazeli, Romain [1 ]
Coutard, Michele [2 ,3 ]
Duport, Benjamin Daumas [2 ,3 ]
Lancelot, Eric [4 ]
Corot, Claire [4 ]
Laissy, Jean-Pierre [1 ,2 ,3 ]
Letourneur, Didier [2 ,3 ]
Michel, Jean-Baptiste [2 ,3 ]
Serfaty, Jean-Michel [1 ,2 ,3 ]
机构
[1] Hop Xavier Bichat, Dept Radiol, Paris, France
[2] INSERM, U698, Paris, France
[3] Univ Paris 07, U698, Paris, France
[4] Roissy, Guerbet Res, Paris, France
关键词
aneurysms; matrix metalloproteinases; magnetic resonance imaging; molecular probe; ATHEROSCLEROSIS; INFLAMMATION; RUPTURE; PATHOGENESIS; THROMBUS; PROBE; RATS; MRI;
D O I
10.1097/RLI.0b013e3181ee5bbf
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
Objective: Abdominal aortic aneurysm (AAA) rupture is a devastating event, and development of noninvasive methods to detect AAA at risk is needed. Matrix metalloproteinases (MMPs) play a major role in AAA growth and their subsequent rupture. This study was aimed to evaluate the ability of P947, a recently developed magnetic resonance imaging (MRI) contrast agent, to target MMPs in vivo in expanding experimental AAAs. Materials and Methods: AAAs were induced in Wistar rats (n = 18) by perfusion of a segment of the abdominal aorta with porcine elastase. After 5 or 6 days of elastase perfusion, when the aortic segment was expanding and showed inflammation with high MMP levels, rats were injected either with P947 (n = 6), P1135, a scramble form of P947 (n = 6), or with the reference contrast agent Gadolinium-DOTA (Gd-DOTA) (n = 3). Sham-operated rats (n = 3) were injected with P947 as controls. Imaging was performed on the animals using a 1.5T MRI scanner before and at different times after injection of contrast agents (100 mu mol/kg). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gelatin zymography of culture media conditioned by incubation with perfused aortic segment or control TA from elastase-perfused rats (n = 3) was performed to determine levels of MMP2 and MMP9. In addition, in situ gelatin zymography was used to localize these active MMPs on frozen histologic sections. Results: The normalized signal enhancement determined on MRI images was higher in the perfused aortic segment of rats injected with P947 (162%) than in rats injected with P1135 (100%) or Gd-DOTA (117%) (P < 0.01 using the Friedman test) from 5 to 125 minutes after injection. The area of contrast enhancement on MRI images colocalized with the fluorescence generated by MMPs in the AAA inflammatory area, as detected by in situ zymography on histologic sections. Conclusion: Our data showed that MRI using P947 allows detection of MMP activity within the inflammatory wall of experimental AAAs, thus representing a potential noninvasive method to detect AAAs with a high risk of rupture.
引用
收藏
页码:662 / 668
页数:7
相关论文
共 33 条
[1]   Biomimetic MRI Contrast Agent for Imaging of Inflammation in Atherosclerotic Plaque of ApoE-/- Mice A Pilot Study [J].
Alsaid, Hasan ;
De Souza, Genevieve ;
Bourdillon, Marie-Claude ;
Chaubet, Frederic ;
Sulaiman, Abdulrazzag ;
Desbleds-Mansard, Catherine ;
Chaabane, Linda ;
Zahir, Charaf ;
Lancelot, Eric ;
Rousseaux, Olivier ;
Corot, Claire ;
Douek, Philippe ;
Briguet, Andre ;
Letourneur, Didier ;
Canet-Soulas, Emmanuelle .
INVESTIGATIVE RADIOLOGY, 2009, 44 (03) :151-158
[2]   Atherosclerosis and Matrix Metalloproteinases: Experimental Molecular MR Imaging in Vivo [J].
Amirbekian, Vardan ;
Aguinaldo, Juan Gilberto S. ;
Amirbekian, Smbat ;
Hyafil, Fabien ;
Vucic, Esad ;
Sirol, Marc ;
Weinreb, David B. ;
Le Greneur, Soizic ;
Lancelot, Eric ;
Corot, Claire ;
Fisher, Edward A. ;
Galis, Zorina S. ;
Fayad, Zahi A. .
RADIOLOGY, 2009, 251 (02) :429-438
[3]   ELASTASE-INDUCED EXPERIMENTAL ANEURYSMS IN RATS [J].
ANIDJAR, S ;
SALZMANN, JL ;
GENTRIC, D ;
LAGNEAU, P ;
CAMILLERI, JP ;
MICHEL, JB .
CIRCULATION, 1990, 82 (03) :973-981
[4]  
Ballard DJ, 2000, COCHRANE DB SYST REV, V2
[5]   PROTEOLYTIC REMODELING OF EXTRACELLULAR-MATRIX [J].
BIRKEDALHANSEN, H .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (05) :728-735
[6]   Risk factors for aneurysm rupture in patients kept under ultrasound surveillance [J].
Brown, LC ;
Powell, JT .
ANNALS OF SURGERY, 1999, 230 (03) :289-296
[7]   Near-infrared fluorescent Imaging of matrix metalloproteinase activity after myocardial infarction [J].
Chen, JQ ;
Tung, CH ;
Allport, JR ;
Chen, S ;
Weissleder, R ;
Huang, PL .
CIRCULATION, 2005, 111 (14) :1800-1805
[8]   Transient exposure to elastase induces mouse aortic wall smooth muscle cell production of MCP-1 and RANTES during development of experimental aortic aneurysm [J].
Colonnello, JS ;
Hance, KA ;
Shames, ML ;
Wyble, CW ;
Ziporin, SJ ;
Leidenfrost, JE ;
Ennis, TL ;
Upchurch, GR ;
Thompson, RW .
JOURNAL OF VASCULAR SURGERY, 2003, 38 (01) :138-146
[9]   High-flow-induced arterial remodeling in rats with different susceptibilities to cerebral aneurysms [J].
Coutard, Michele ;
Osborne-Pellegrin, Mary ;
Fontaine, Vincent ;
Jacob, Marie-Paule ;
Michel, Jean-Baptiste .
JOURNAL OF VASCULAR RESEARCH, 2006, 43 (03) :217-228
[10]   Inflammation in atherosclerosis - Visualizing matrix metalloproteinase action in macrophages in vivo [J].
Deguchi, Jun-o ;
Aikawa, Masanori ;
Tung, Ching-Hsuan ;
Aikawa, Elena ;
Kim, Dong-Eog ;
Ntziachristos, Vasilis ;
Weissleder, Ralph ;
Libby, Peter .
CIRCULATION, 2006, 114 (01) :55-62