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人乳动脉器官培养中支架置入后的新生内膜增生。

Neointimal hyperplasia after stenting in a human mammary artery organ culture.

作者信息

Guérin P, Rondeau F, Grimandi G, Heymann M F, Heymann D, Pillet P, Al Habash O, Loirand G, Pacaud P, Crochet D

机构信息

Laboratoire EE 9901, CHU Nantes, Nantes, France.

出版信息

J Vasc Res. 2004 Jan-Feb;41(1):46-53. doi: 10.1159/000076245. Epub 2004 Jan 16.

Abstract

Although the use of stents has limited the incidence of restenosis, in-stent restenosis remains an important problem. In-stent restenosis is the result of a healing process that induced neointimal hyperplasia through mechanisms that are still not understood. The aim of this study was to analyze the histological consequences of the healing process following stent implantation. Internal mammary arteries from atheroslerotic patients undergoing coronary artery bypass surgery were stented and maintained in culture for 0-28 days. Stent implantation after predilatation induced an extensive loss of endothelial cells whereas direct stenting preserved endothelium between the struts. Morphometric analysis shows that stent placement induced neointimal thickening. Smooth muscle alpha-actin labeling indicates that neo-intimal formation was mainly due to proliferation and migration of smooth muscle cells. Smooth muscle cell proliferation, assessed by MIB-1 staining, was maximal at day 14 after stent insertion. Human mammary artery organ culture thus provides valuable information on histological consequences of stent implantation with or without predilatation regarding endothelial cell disappearance and neointimal hyperplasia. These data also demonstrate that neointimal thickening induced by stent implantation comprises an intrinsic component resulting from the vessel wall response to stent insertion and suggest that blood factors could play an amplifying but not necessary role.

摘要

尽管支架的使用已降低了再狭窄的发生率,但支架内再狭窄仍是一个重要问题。支架内再狭窄是一种愈合过程的结果,该过程通过尚不清楚的机制诱导了新生内膜增生。本研究的目的是分析支架植入后愈合过程的组织学后果。对接受冠状动脉搭桥手术的动脉粥样硬化患者的乳内动脉进行支架置入,并在培养中维持0 - 28天。预扩张后植入支架导致内皮细胞大量丢失,而直接支架置入可保留支架小梁间的内皮。形态计量分析表明,支架置入可诱导新生内膜增厚。平滑肌α -肌动蛋白标记显示,新生内膜形成主要归因于平滑肌细胞的增殖和迁移。通过MIB - 1染色评估,平滑肌细胞增殖在支架置入后第14天达到最大值。因此,人乳动脉器官培养为有或无预扩张的支架植入在内皮细胞消失和新生内膜增生方面的组织学后果提供了有价值的信息。这些数据还表明,支架植入诱导的新生内膜增厚包括血管壁对支架置入反应产生的内在成分,并提示血液因素可能起放大作用,但并非必要作用。

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