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Endothelial effects of antihypertensive treatment: focus on irbesartan

机译:降压治疗的内皮效应:以厄贝沙坦为重点

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The endothelium is characterized by a wide range of important homeostatic functions. It participates in the control of hemostasis, blood coagulation and fibrinolysis, platelet and leukocyte interactions with the vessel wall, regulation of vascular tone, and of blood pressure. Many crucial vasoactive endogenous compounds are produced by the endothelial cells to control the functions of vascular smooth muscle cells and of circulating blood cells. These complex systems determine a fine equilibrium which regulates the vascular tone. Impairments in endothelium-dependent vasodilation lead to the so called endothelial dysfunction. Endothelial dysfunction is then characterized by unbalanced concentrations of vasodilating and vasoconstricting factors, the most important being represented by nitric oxide (NO) and angiotensin II (AT II). High angiotensin-converting enzyme (ACE) activity leads to increased AT II generation, reduced NO levels with subsequent vasoconstriction. The net acute effect results in contraction of vascular smooth muscle cells and reduced lumen diameter. Furthermore, when increased ACE activity is chronically sustained, increase in growth, proliferation and differentiation of the vascular smooth muscle cells takes place; at the same time, a decrease in the anti-proliferative action by NO, a decrease in fibinolysis and an increase in platelets aggregation may be observed. AT II is then involved not only in the regulation of blood pressure, but also in vascular inflammation, permeability, smooth muscle cells remodelling, and oxidative stress which in turn lead to atherosclerosis and increased cardiovascular risk. Given the pivotal role exerted by AT II in contributing to alteration of endothelial function, treatment with ACE inhibitors or angiotensin receptor blockers (ARBs) may be of particular interest to restore a physiological activity of endothelial cells. In this view, the blockade of the renin-angiotensin system (RAS), has been shown to positively affect the endothelial function, beyond the antihypertensive action displayed by these compounds. In this review, attention has been specifically focused on an ARB, irbesartan, to examine its effects on endothelial function.
机译:内皮的特征在于广泛的重要稳态功能。它参与止血,凝血和纤维蛋白溶解,血小板和白细胞与血管壁的相互作用,血管张力和血压调节的控制。内皮细胞产生许多重要的血管活性内源性化合物,以控制血管平滑肌细胞和循环血细胞的功能。这些复杂的系统决定了调节血管张力的良好平衡。内皮依赖性血管舒张功能受损会导致所谓的内皮功能障碍。内皮功能障碍的特征是血管扩张和血管收缩因子的浓度不平衡,最重要的是一氧化氮(NO)和血管紧张素II(AT II)。血管紧张素转换酶(ACE)的高活性导致AT II生成增加,NO水平降低以及随后的血管收缩。净急性作用导致血管平滑肌细胞收缩和管腔直径减小。此外,当长期持续维持增加的ACE活性时,血管平滑肌细胞的生长,增殖和分化就会增加。同时,可以观察到NO引起的抗增殖作用降低,纤维蛋白溶解降低和血小板聚集增加。然后,AT II不仅涉及血压的调节,还涉及血管炎症,通透性,平滑肌细胞重塑和氧化应激,进而导致动脉粥样硬化和心血管风险增加。考虑到AT II在促进内皮功能改变中所起的关键作用,使用ACE抑制剂或血管紧张素受体阻滞剂(ARB)进行治疗对于恢复内皮细胞的生理活性可能特别有意义。以这种观点,已经证明,肾素-血管紧张素系统(RAS)的阻滞除了对这些化合物所表现出的降压作用外,还对内皮功能产生积极影响。在本综述中,注意力特别集中在ARB厄贝沙坦上,以检查其对内皮功能的影响。

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