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血管重塑:对小动脉功能和靶器官损伤的影响

Vascular remodeling: implications for small artery function and target organ damage.

作者信息

Sonoyama Kazuhiko, Greenstein Adam, Price Anna, Khavandi Kaivan, Heagerty Tony

机构信息

Division of Cardiovascular and Endocrine Sciences, University of Manchester, UK.

出版信息

Ther Adv Cardiovasc Dis. 2007 Dec;1(2):129-37. doi: 10.1177/1753944707086358.

Abstract

At the level of the small artery, essential hypertension is associated with eutrophic inward remodeling. This involves reduction in lumen diameter by an increase in wall thickness. Previously thought to involve either hypertrophy or hyperplasia of the vascular smooth muscle cells in the media, it is now felt to be mediated by a functional property of the wall: myogenic tone. This is the ability of an artery to contract in response to an increase in intraluminal pressure. This autoregulatory function is also vital to ensure stabilisation of distal capillary pressures and so prevent, or limit, organ damage. Indeed in any animal model studied, when myogenic autoregulation is affected, target organ damage ensues. We have also observed, in two studies, that when myogenic autoregulation is damaged in the context of hypertension, eutrophic remodeling is replaced by an outward growth of the arterial wall with preservation of lumen diameter. This is called hypertrophic remodeling and, independently, has been observed by a number of groups in small arteries from patients with type 2 diabetes. We believe that this is a key reason for the unique propensity to hypertensive injury seen in patients with diabetes. We also discuss the significance of integrins, transmembrane proteins with wide ranging functions; from initiation of cell migration to intracellular signalling. Two particular integrins, alpha5beta1 and alphanubeta3, have been found to be necessary for both normal myogenic autoregulation and eutrophic remodeling and the possibility that damage to these may occur in diabetes is examined.

摘要

在小动脉水平,原发性高血压与营养正常的内向重塑有关。这涉及通过增加壁厚来减小管腔直径。以前认为这涉及中膜血管平滑肌细胞的肥大或增生,现在认为这是由血管壁的一种功能特性介导的:肌源性张力。这是动脉对管腔内压力增加做出收缩反应的能力。这种自动调节功能对于确保远端毛细血管压力的稳定以及预防或限制器官损伤也至关重要。事实上,在任何研究的动物模型中,当肌源性自动调节受到影响时,靶器官损伤就会发生。我们还在两项研究中观察到,在高血压背景下肌源性自动调节受损时,营养正常的重塑会被动脉壁的向外生长所取代,管腔直径得以保留。这被称为肥厚性重塑,并且多个研究小组在2型糖尿病患者的小动脉中也独立观察到了这一现象。我们认为这是糖尿病患者出现高血压损伤独特倾向的一个关键原因。我们还讨论了整合素的重要性,整合素是具有广泛功能的跨膜蛋白,从细胞迁移的启动到细胞内信号传导。已经发现两种特定的整合素,α5β1和ανβ3,对于正常的肌源性自动调节和营养正常的重塑都是必需的,并且研究了糖尿病中这些整合素可能受损的可能性。

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