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肾素-血管紧张素-醛固酮系统在血管重塑和炎症中的作用:一项临床综述

Role of the renin-angiotensin-aldosterone system in vascular remodeling and inflammation: a clinical review.

作者信息

Duprez Daniel A

机构信息

Cardiovascular Division, Medical School, University of Minnesota, Minneapolis 55455, USA.

出版信息

J Hypertens. 2006 Jun;24(6):983-91. doi: 10.1097/01.hjh.0000226182.60321.69.

Abstract

The concept of hypertension as primarily a consequence of altered hemodynamics has changed. Many factors are now implicated in the development of hypertensive vascular disease, and the renin-angiotensin-aldosterone system (RAAS) appears to be one of the most significant. Angiotensin II, the principal effector peptide of the RAAS, has far-reaching effects on vascular structure, growth and fibrosis, and is a key regulator of vascular remodeling and inflammation. Reactive oxygen species and a network of signaling pathways mediate angiotensin II and cellular mechanisms that promote remodeling and inflammation. The involvement of aldosterone in vessel-wall and myocardial remodeling has also come under intensive research scrutiny. Treatments that block the pathologic effects of the RAAS at several points have been shown to limit target-organ damage in hypertension and to decrease cardiovascular morbidity and mortality. Understanding the molecular and cellular mechanisms that participate in the early development of hypertensive vascular disease may lead to more targeted treatment and improved outcomes.

摘要

高血压主要是血流动力学改变所致的这一概念已经发生了变化。现在许多因素都与高血压性血管疾病的发展有关,而肾素-血管紧张素-醛固酮系统(RAAS)似乎是最重要的因素之一。血管紧张素II是RAAS的主要效应肽,对血管结构、生长和纤维化具有深远影响,并且是血管重塑和炎症的关键调节因子。活性氧和信号通路网络介导血管紧张素II以及促进重塑和炎症的细胞机制。醛固酮在血管壁和心肌重塑中的作用也受到了深入的研究审视。在多个环节阻断RAAS病理效应的治疗方法已被证明可限制高血压患者的靶器官损害,并降低心血管发病率和死亡率。了解参与高血压性血管疾病早期发展的分子和细胞机制可能会带来更具针对性的治疗并改善治疗效果。

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