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剪切应力与血流介导的血管舒张之间的关系:对内皮功能评估的意义。

The relationship between shear stress and flow-mediated dilatation: implications for the assessment of endothelial function.

作者信息

Pyke Kyra E, Tschakovsky Michael E

机构信息

Human Vascular Control Laboratory, School of Physical and Health Education, Queen's University, Kingston, ON, Canada.

出版信息

J Physiol. 2005 Oct 15;568(Pt 2):357-69. doi: 10.1113/jphysiol.2005.089755. Epub 2005 Jul 28.

Abstract

Endothelium-dependent flow-mediated dilatation (FMD) describes the vasodilatory response of a vessel to elevations in blood flow-associated shear stress. Nitric oxide (NO), one of many vasoactive substances released by the endothelium in response to shear stress, is of particular interest to researchers as it is an antiatherogenic molecule, and a reduction in its bioavailability may play a role in the pathogenesis of vascular disease. The goal of many human studies is to create a shear stress stimulus that produces an NO-dependent response in order to use the FMD measurements as an assay of NO bioavailability. The most common non-invasive technique is the 'reactive hyperaemia test' which produces a large, transient shear stress profile and a corresponding FMD. Importantly, not all FMD is NO mediated and the stimulus creation technique is a critical determinant of NO dependence. The purpose of this review is to (1) explain that the mechanisms of FMD depend on the nature of the shear stress stimulus (stimulus response specificity), (2) provide an update to the current guidelines for FMD assessment, and (3) summarize the issues that surround the clinical utility of measuring both NO- and non-NO-mediated FMD. Future research should include (1) the identification and partitioning of mechanisms responsible for FMD in response to various shear stress profiles, (2) investigation of stimulus response specificity in coronary arteries, and (3) investigation of non-NO FMD mechanisms and their connection to the development of vascular disease and occurrence of cardiovascular events.

摘要

内皮依赖性血流介导的血管舒张(FMD)描述了血管对与血流相关的剪切应力升高的血管舒张反应。一氧化氮(NO)是内皮细胞在对剪切应力作出反应时释放的多种血管活性物质之一,因其是一种抗动脉粥样硬化分子,其生物利用度的降低可能在血管疾病的发病机制中起作用,所以特别受到研究人员的关注。许多人体研究的目标是创建一种能产生依赖NO反应的剪切应力刺激,以便将FMD测量用作NO生物利用度的检测方法。最常见的非侵入性技术是“反应性充血试验”,它会产生一个大的、短暂的剪切应力曲线和相应的FMD。重要的是,并非所有的FMD都是由NO介导的,刺激创建技术是NO依赖性的关键决定因素。本综述的目的是:(1)解释FMD的机制取决于剪切应力刺激的性质(刺激反应特异性);(2)更新当前FMD评估指南;(3)总结围绕测量NO介导和非NO介导的FMD临床效用的问题。未来的研究应包括:(1)识别和区分对各种剪切应力曲线作出反应时导致FMD的机制;(2)研究冠状动脉中的刺激反应特异性;(3)研究非NO介导的FMD机制及其与血管疾病发展和心血管事件发生的关联。

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