Is hypertension a tissue perfusion disorder? Implications for renal and myocardial perfusion.

Jean-Jacques Mourad, Maurice Laville
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引用次数: 22

Abstract

Structural alterations in the microcirculation form a major link between hypertension and target organ damage. More than 60% of the overall peripheral resistance of the circulatory system arises at the level of the microcirculation. The primary function of the microcirculation is to supply oxygen and nutrients to tissues. In hypertension, remodelling of the microvascular vessels occurs, leading to an early, functional then anatomical reduction in the number of arterioles or capillaries in a given vascular bed. Such changes have been seen in the structure and density of the microvasculature of different target organs such as the myocardium and the kidneys. In hypertension, capillary rarefaction induces an increase in blood pressure, a relative decrease in tissue perfusion and an increased cardiovascular risk. Recent in-vivo non-invasive techniques for exploring the human microcirculation have allowed the detection of myocardial and renal microvascular impairment in hypertensive patients. In comparative therapeutic studies, antihypertensive drugs have been shown to have different capacities for preventing or reversing changes to the microvasculature of affected organs.

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高血压是组织灌注紊乱吗?对肾脏和心肌灌注的影响。
微循环结构改变是高血压和靶器官损伤之间的主要联系。循环系统总外周阻力的60%以上产生于微循环水平。微循环的主要功能是为组织提供氧气和营养。在高血压患者中,微血管发生重构,导致给定血管床中小动脉或毛细血管数量的早期、功能性和解剖学上的减少。这种变化在不同靶器官如心肌和肾脏的微血管的结构和密度中已被观察到。在高血压中,毛细血管稀疏导致血压升高、组织灌注相对减少和心血管风险增加。最近的体内无创技术用于探索人体微循环,可以检测高血压患者的心肌和肾脏微血管损伤。在比较治疗研究中,降压药物已被证明在预防或逆转受影响器官微血管变化方面具有不同的能力。
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