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Title
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Multi-slice computed tomography with N1177 identifies ruptured atherosclerotic plaques in rabbits
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Author
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Abstract
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| Rupture-prone and ruptured plaques are characterized by the presence of large numbers of macrophages. N1177 is a contrast agent consisting of iodinated nanoparticles that are selectively phagocytosed by macrophages. The aim of this study was to investigate the effect of N1177 on the CT attenuation of rupture-prone and ruptured plaques in rabbits. In addition, we examined in vitro whether uptake of N1177 occurred without cytotoxic or pro-inflammatory effects on macrophages. In vitro, the viability of J774 macrophages was not affected by treatment with N1177. Moreover, N1177 had no effect on the phagocytic capacity or cytokine production of macrophages. For the in vivo experiments, 6 New Zealand White rabbits were fed a cholesterol-supplemented diet for 1215 months, resulting in the development of large atherosclerotic plaques that resembled rupture-prone plaques in humans. In three rabbits, mechanical plaque rupture was induced by retrograde pullback of an embolic protection device. N1177 had no effect on the median density of rupture-prone plaques [35 HU (range 385) before injection vs. 32 HU (range 193) 2 h after injection of N1177; P > 0.05]. However, after induction of mechanical plaque rupture, the median density of the atherosclerotic plaques increased from 40 HU (range 686) before injection to 74 HU (range 14111) 2 h after injection of N1177 (P < 0.001). Using time-of-flight static secondary ion mass spectrometry, the presence of N1177 nanoparticles was demonstrated in macrophage-rich areas of ruptured plaques, but not of non-ruptured plaques. In conclusion, our results show that N1177 is a contrast agent that can identify ruptured atherosclerotic plaques. |
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Language
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English
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Source (journal)
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Basic research in cardiology. - Darmstadt
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Publication
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Darmstadt
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2010
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ISSN
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0300-8428
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DOI
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10.1007/S00395-009-0052-0
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Volume/pages
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105
:1
(2010)
, p. 51-59
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ISI
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000272530000007
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Full text (Publisher's DOI)
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Full text (publisher's version - intranet only)
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