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人类的内皮功能与缓激肽

Endothelial function and bradykinin in humans.

作者信息

Hornig B, Drexler H

机构信息

Abteilung Kardiologie, Medizinische Hochschule Hannover, Germany.

出版信息

Drugs. 1997;54 Suppl 5:42-7. doi: 10.2165/00003495-199700545-00007.

Abstract

The endothelium controls vascular smooth muscle tone by secreting relaxing and contracting factors. There is a constant release of endothelium-derived relaxing factors (EDRFs) under basal conditions. In addition, the endothelium can increase the release of EDRFs in response to humoral stimulation by vasoactive substances such as acetylcholine or bradykinin. Under physiological conditions, the most important stimulus to the release of EDRFs is an increase in blood flow leading to increased shear stress on endothelial cells. Recent experimental studies raised the possibility that bradykinin plays an important role in the regulation of vascular tone at rest and during flow-stimulated conditions. Bradykinin is a very potent vasodilator that exerts its vasodilatory actions by causing endothelial release of nitric oxide, prostacyclin and/or a hyperpolarising factor [endothelium-derived hyperpolarising factor (EDHF)]. This concept is also supported by recent studies in humans demonstrating that bradykinin contributes to the regulation of coronary vascular tone under resting and flow-stimulated conditions. This mechanism has now been shown to be important in both human peripheral and coronary arteries. Angiotensin converting enzyme (ACE) inhibitors not only reduce angiotensin II, but also increase bradykinin levels, since the angiotensin converting enzyme is identical to kininase II, an enzyme that degrades bradykinin. This raises the possibility that beneficial vascular effects of ACE inhibitors may be related to increased availability of bradykinin. Indeed, we have recently shown that ACE inhibition improves flow-dependent, endothelium-mediated vasodilation and that this beneficial effect of ACE inhibition is bradykinin dependent. These findings raise the possibility that the beneficial effects of ACE inhibition in heart failure and coronary artery disease might be partly due to improved endothelial function.

摘要

内皮细胞通过分泌舒张和收缩因子来控制血管平滑肌张力。在基础条件下,内皮衍生舒张因子(EDRFs)持续释放。此外,内皮细胞可响应血管活性物质如乙酰胆碱或缓激肽的体液刺激,增加EDRFs的释放。在生理条件下,EDRFs释放的最重要刺激因素是血流增加,导致内皮细胞上的剪切应力增加。最近的实验研究提出,缓激肽在静息和血流刺激条件下的血管张力调节中起重要作用。缓激肽是一种非常强效的血管舒张剂,通过促使内皮细胞释放一氧化氮、前列环素和/或超极化因子[内皮衍生超极化因子(EDHF)]来发挥其血管舒张作用。这一概念也得到了最近人体研究的支持,这些研究表明缓激肽在静息和血流刺激条件下有助于冠状动脉张力的调节。现已证明这一机制在人体外周动脉和冠状动脉中均很重要。血管紧张素转换酶(ACE)抑制剂不仅能降低血管紧张素II,还能增加缓激肽水平,因为血管紧张素转换酶与激肽酶II相同,激肽酶II是一种降解缓激肽的酶。这就增加了ACE抑制剂有益的血管效应可能与缓激肽可用性增加有关的可能性。事实上,我们最近表明,ACE抑制可改善血流依赖性、内皮介导的血管舒张,且ACE抑制的这种有益作用依赖于缓激肽。这些发现增加了ACE抑制在心力衰竭和冠状动脉疾病中的有益作用可能部分归因于内皮功能改善的可能性。

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