载脂蛋白E基因敲除小鼠头臂动脉完整和破裂的动脉粥样硬化斑块特征

H. Williams, Jason L. Johnson, K. Carson, C. Jackson
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引用次数: 233

摘要

脂肪喂养的载脂蛋白E敲除小鼠的头臂动脉形成斑块,经常破裂并形成管腔血栓。现在已经定义了没有不稳定证据或先前破裂(完整)愈合的斑块和急性破裂斑块(破裂)的血管的形态学特征,以便更详细地了解斑块不稳定的过程。98只载脂蛋白E敲除小鼠饲喂添加21%猪油和0.15%胆固醇的饲粮,为期5 ~ 59周。在这98只小鼠中,51只在头臂动脉中有急性破裂的斑块。破裂斑块和完整斑块的横截面积不同(完整斑块,0.109±0.016 mm2;破裂,0.192±0.009 mm2, P =0.0005),管腔闭塞(完整,35.3±3.3%;破裂,57.7±1.9%,P <0.0001),病变内埋帽数(完整,1.06±0.12;破裂,2.66±0.16;P <0.0001),纤维帽厚度(完整,4.7±0.6;m;破裂,2.0±0.3 &mgr;m;P =0.0004),脂质分数体积(完整,35.9±3.0%;破裂,50.7±2.2%;P =0.0019)。本研究证实,在高脂肪饮食的载脂蛋白E敲除小鼠的头臂动脉中,斑块破裂是经常发生的。数据还表明,这些小鼠的破裂斑块显示出人类易损斑块的许多特征。这支持了该模型在斑块破裂机制和治疗研究中的应用。
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Characteristics of Intact and Ruptured Atherosclerotic Plaques in Brachiocephalic Arteries of Apolipoprotein E Knockout Mice
The brachiocephalic arteries of fat-fed apolipoprotein E knockout mice develop plaques that frequently rupture and form luminal thromboses. The morphological characteristics of plaques without evidence of instability or with healed previous ruptures (intact) and vessels with acutely ruptured plaques (ruptured) have now been defined, to understand the process of plaque destabilization in more detail. Ninety-eight apolipoprotein E knockout mice were fed a diet supplemented with 21% lard and 0.15% cholesterol, for 5 to 59 weeks. Of these 98 mice, 51 had an acutely ruptured plaque in the brachiocephalic artery. Ruptured and intact plaques differed in terms of plaque cross-sectional area (intact, 0.109±0.016 mm2; ruptured, 0.192±0.009 mm2;P =0.0005), luminal occlusion (intact, 35.3±3.3%; ruptured, 57.7±1.9%;P <0.0001), the number of buried caps within the lesion (intact, 1.06±0.12; ruptured, 2.66±0.16;P <0.0001), fibrous cap thickness (intact, 4.7±0.6 &mgr;m; ruptured, 2.0±0.3 &mgr;m;P =0.0004), and lipid fractional volume (intact, 35.9±3.0%; ruptured, 50.7±2.2%;P =0.0019). This study confirms that plaque rupture is a frequent occurrence in the brachiocephalic arteries of apolipoprotein E knockout mice on a high-fat diet. The data also show that ruptured plaques in these mice show many of the characteristics of vulnerable plaques in humans. This supports the use of this model in studies of the mechanisms and therapy of plaque rupture.
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