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载脂蛋白E基因敲除小鼠无名动脉中的晚期动脉粥样硬化病变。

Advanced atherosclerotic lesions in the innominate artery of the ApoE knockout mouse.

作者信息

Rosenfeld M E, Polinsky P, Virmani R, Kauser K, Rubanyi G, Schwartz S M

机构信息

Department of Pathology, University of Washington, Seattle 98195, USA.

出版信息

Arterioscler Thromb Vasc Biol. 2000 Dec;20(12):2587-92. doi: 10.1161/01.atv.20.12.2587.

Abstract

Most previous studies of atherosclerosis in hyperlipidemic mouse models have focused their investigations on lesions within the aorta or aortic sinus in young animals. None of these studies has demonstrated clinically significant advanced lesions. We previously mapped the distribution of lesions throughout the arterial tree of apolipoprotein E knockout (apoE(-/-)) mice between the ages of 24 and 60 weeks. We found that the innominate artery, a small vessel connecting the aortic arch to the right subclavian and right carotid artery, exhibits a highly consistent rate of lesion progression and develops a narrowed vessel characterized by atrophic media and perivascular inflammation. The present study reports the characteristics of advanced lesions in the innominate artery of apoE(-/-) mice aged 42 to 60 weeks. In animals aged 42 to 54 weeks, there is a very high frequency of intraplaque hemorrhage and a fibrotic conversion of necrotic zones accompanied by loss of the fibrous cap. By 60 weeks of age, the lesions are characterized by the presence of collagen-rich fibrofatty nodules often flanked by lateral xanthomas. The processes underlying these changes in the innominate artery of older apoE(-/-) mice could well be a model for the critical processes leading to the breakdown and healing of the human atherosclerotic plaque.

摘要

以往大多数关于高脂血症小鼠模型动脉粥样硬化的研究都将重点放在了幼龄动物主动脉或主动脉窦内的病变上。这些研究均未证实存在具有临床意义的晚期病变。我们之前绘制了24至60周龄载脂蛋白E基因敲除(apoE(-/-))小鼠整个动脉树中病变的分布情况。我们发现无名动脉,即连接主动脉弓与右锁骨下动脉和右颈动脉的一条小血管,呈现出高度一致的病变进展速率,并形成了以中膜萎缩和血管周围炎症为特征的血管狭窄。本研究报告了42至60周龄apoE(-/-)小鼠无名动脉晚期病变的特征。在42至54周龄的动物中,斑块内出血的频率非常高,坏死区域发生纤维化转变,同时伴有纤维帽的缺失。到60周龄时,病变的特征是存在富含胶原蛋白的纤维脂肪结节,其两侧常伴有黄色瘤。老年apoE(-/-)小鼠无名动脉这些变化背后的过程很可能是导致人类动脉粥样硬化斑块破裂和愈合的关键过程的一个模型。

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