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非人类灵长类动物高胆固醇血症的研究。II. 脂纹向纤维斑块的转变。

Studies of hypercholesterolemia in the nonhuman primate. II. Fatty streak conversion to fibrous plaque.

作者信息

Faggiotto A, Ross R

出版信息

Arteriosclerosis. 1984 Jul-Aug;4(4):341-56. doi: 10.1161/01.atv.4.4.341.

Abstract

This report presents the second portion of the morphologic studies on chronic, diet-induced hypercholesterolemia in nonhuman primates (Macaca nemestrina) examined sequentially between 5 and 13 months. A direct relationship was observed between the rate of cholesterol increase, the level and duration of hypercholesterolemia, and the changes in the artery wall that led to the formation of fatty streaks and their conversion to fibrous plaques. A loss of endothelial continuity was first observed in the iliac arteries between 3 and 4 months of atherogenic diet and appears to be a critical step in the conversion of many fatty streaks to fibrous plaques. With breaks in endothelial junctions and exposure of some of the macrophages in a fatty streak, many of the lipid-filled macrophages appeared to detach and enter the circulation. The number of circulating foam cells increased precipitously between 3 and 4 months, the time when increased sites of endothelial dysjunction and macrophage egress were observed. Exposure of subendothelial macrophages also permitted adherence of platelets to these macrophages and to exposed connective tissue. Fibrous plaques were found at similar anatomic sites where endothelial denudation had been observed at earlier time points but were more prevalent in the abdominal aorta and iliac arteries. These changes subsequently occurred at every level of the aortic tree and appeared to progress in a cephalad fashion with increasing rate, level, and duration of hypercholesterolemia. The results of these studies stress the importance of following cholesterol levels of each animal throughout the entire period of the study and of sampling the entire arterial tree at every level with time. This helped us to understand the complicated interrelationships between the various cells in atherogenesis, provided further support for the "Response to Injury Hypothesis of Atherosclerosis," and helped to explain how hypercholesterolemia may be involved in the different stages of atherogenesis in nonhuman primates and possibly in humans.

摘要

本报告展示了对食蟹猴(Macaca nemestrina)慢性饮食诱导高胆固醇血症进行形态学研究的第二部分内容,这些食蟹猴在5至13个月期间被依次检查。研究观察到胆固醇升高速率、高胆固醇血症水平和持续时间与动脉壁变化之间存在直接关系,这些变化导致了脂肪条纹的形成及其向纤维斑块的转变。在致动脉粥样硬化饮食3至4个月时,首次在髂动脉中观察到内皮连续性丧失,这似乎是许多脂肪条纹转变为纤维斑块的关键步骤。随着内皮连接中断以及脂肪条纹中的一些巨噬细胞暴露,许多充满脂质的巨噬细胞似乎脱离并进入循环。在3至4个月期间,循环泡沫细胞数量急剧增加,此时观察到内皮功能障碍和巨噬细胞外渗的部位增多。内皮下巨噬细胞的暴露也使血小板能够黏附于这些巨噬细胞以及暴露的结缔组织。在早期观察到内皮剥脱的相似解剖部位发现了纤维斑块,但在腹主动脉和髂动脉中更为普遍。这些变化随后在主动脉树的各个层面出现,并似乎随着高胆固醇血症的速率、水平和持续时间增加而呈头向进展。这些研究结果强调了在整个研究期间跟踪每只动物胆固醇水平以及随时间对主动脉树各个层面进行采样的重要性。这有助于我们理解动脉粥样硬化形成过程中各种细胞之间复杂的相互关系,为“动脉粥样硬化损伤反应假说”提供了进一步支持,并有助于解释高胆固醇血症如何参与食蟹猴乃至可能人类动脉粥样硬化形成的不同阶段。

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