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动脉粥样硬化的发病机制。

Pathogenetic mechanisms in atherosclerosis.

作者信息

Walton K W

出版信息

Am J Cardiol. 1975 Apr;35(4):542-58. doi: 10.1016/0002-9149(75)90839-5.

Abstract

Four theories of atherogenesis are briefly reviewed and criticized: the degenerative, the thrombogenic, the platelet aggregation and the insudative theory. Evidence is presented in detail to suggest that a modified form of the insudative theory (1) accounts more satisfactorily than the other theories for the known association of risk factors with atherosclerosis and (2) allows one to understand how some of the more important risk factors operate at the level of the arterial wall. It is proposed that atherosclerotic plaques, and also certain extravascular lesions broadly associated with atherosclerosis (corneal arcus, xanthomas), arise because altered endothelial permeability allows certain reactive macromolecular plasma proteins (the plasma low density and very low density lipoproteins and fibrinogen, which are normally largely confined to the circulation) to permeate endothelium and interact with charged components of the connective tissue gel of the arterial wall or other tissues. The effect of hyperlipidemia, hypertension, arterial disease or injury upon this process, and the manner in which these factors interact, is examined in relation to experimental findings and clinical observations.

摘要

本文简要回顾并批判了动脉粥样硬化形成的四种理论

退行性理论、血栓形成理论、血小板聚集理论和渗出理论。详细阐述的证据表明,一种改良形式的渗出理论(1)比其他理论更能令人满意地解释已知的风险因素与动脉粥样硬化之间的关联,并且(2)能让人理解一些更重要的风险因素是如何在动脉壁水平发挥作用的。本文提出,动脉粥样硬化斑块以及某些与动脉粥样硬化广泛相关的血管外病变(角膜弓、黄色瘤)的出现,是因为内皮通透性改变使得某些具有反应性的大分子血浆蛋白(血浆低密度脂蛋白、极低密度脂蛋白和纤维蛋白原,它们通常主要局限于循环系统)能够透过内皮,并与动脉壁或其他组织的结缔组织凝胶中的带电成分相互作用。结合实验结果和临床观察,研究了高脂血症、高血压、动脉疾病或损伤对这一过程的影响,以及这些因素相互作用的方式。

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