Pharmacy Department, Faculty of Tech. and Engg., The M. S. University of Baroda, Vadodara 390 001, Gujarat, India.
Bioorg Med Chem. 2010 Dec 15;18(24):8418-56. doi: 10.1016/j.bmc.2010.10.043. Epub 2010 Nov 9.
Hypertension is a major risk factor for human morbidity and mortality through its effects on target organs like heart, brain and kidneys. More intensive treatment for the effective control of blood pressure significantly reduces the morbidity and mortality. The renin angiotensin system (RAS) is a coordinated hormonal cascade of major clinical importance in the regulation of blood pressure. The principal effector peptide of RAS is angiotensin II, which acts by binding to one of the two major angiotensin II receptors AT(1) and AT(2). Angiotensin II through AT(1) receptor mediates vast majority of biologically detrimental actions. Nonpeptidic angiotensin II (AT(1)) antagonists are the most specific means to block the renin angiotensin enzymatic cascade available presently. Majority of AT(1) antagonists are based on modifications of losartan structure, the first clinically used AT(1) antagonist. In this review, a comprehensive presentation of the literature on AT(1) receptor antagonists has been given.
高血压通过对心脏、大脑和肾脏等靶器官的影响,成为人类发病率和死亡率的主要危险因素。更积极的降压治疗可显著降低发病率和死亡率。肾素-血管紧张素系统(RAS)是一个协调的激素级联反应,在调节血压方面具有重要的临床意义。RAS 的主要效应肽是血管紧张素 II,它通过与两种主要的血管紧张素 II 受体 AT(1)和 AT(2)之一结合发挥作用。血管紧张素 II 通过 AT(1)受体介导绝大多数生物学上有害的作用。非肽类血管紧张素 II(AT(1))拮抗剂是目前可获得的阻断肾素-血管紧张素酶级联反应的最特异手段。大多数 AT(1)拮抗剂基于氯沙坦结构的修饰,氯沙坦是第一个临床应用的 AT(1)拮抗剂。在这篇综述中,对 AT(1)受体拮抗剂的文献进行了全面的介绍。