Lancellotti P, Ancion A, D'Orio V, Gach O, Maréchal P, Krzesinski J M
Service de Cardiologie, CHU Sart Tilman, Liège, Belgique.
Service de Néphrologie, Transplantation, Hypertension, CHU Sart Tilman, Liège, Belgique.
Rev Med Liege. 2018 Apr;73(4):197-205.
The endothelium plays a vital role as part of the cardiovascular continuum. Risk factors such as hypertension and dyslipidemia unbalance angiotensin II - bradykinin homeostasis, leading to endothelial dysfunction and changes in vascular structure that promote atherosclerosis and thrombosis. When dealing with risk factors, treatment should focus on the prevention and restoration of endothelial function. Not all cardiovascular drugs are able to reverse vascular and structural endothelial dysfunction. Increasing levels of bradykinin is an effect of the use of angiotensin-converting enzyme inhibitors (ACE-Is), and also a fundamental part of their mode of action. The cardiovascular protection observed with ACE-I, and not with sartans, can be explained rationally by the specific effects of bradykinin on the endothelium. In the pharmacological class of ACE-Is, perindopril likely produces the strongest effects on bradykinin, which may explain, at least in part, the documented superiority of this drug in the prevention and treatment of cardiovascular disease.
内皮作为心血管系统的一部分发挥着至关重要的作用。高血压和血脂异常等危险因素会破坏血管紧张素II - 缓激肽的稳态,导致内皮功能障碍和血管结构改变,进而促进动脉粥样硬化和血栓形成。在应对这些危险因素时,治疗应着重于预防和恢复内皮功能。并非所有心血管药物都能逆转血管和结构性内皮功能障碍。缓激肽水平升高是使用血管紧张素转换酶抑制剂(ACE-Is)的一个作用,也是其作用方式的一个基本部分。ACE-Is所观察到的心血管保护作用(而沙坦类药物没有),可以通过缓激肽对内皮的特定作用得到合理阐释。在ACE-Is这一药理学类别中,培哚普利对缓激肽可能产生最强的作用,这至少可以部分解释该药物在预防和治疗心血管疾病方面已被证实的优越性。