Allikmets Kristina
Department of Drug Development and Medical Affairs, Nycomed Group, Roskilde, Denmark.
Vasc Health Risk Manag. 2007;3(6):809-15.
The importance of renin-angiotensin-aldosterone system (RAAS) in diseases such as hypertension, congestive heart failure and chronic renal failure has long ago been recognized. It has also been established that inhibition of RAAS, using inhibitors of the angiotensin-converting enzyme (ACE) or angiotensin II receptor blockers (ARB), is an effective way to intervene with the pathogenesis of these disorders. Renin inhibitors block the RAAS at the highest level, at its origin, and might thus offer a new exciting approach for pharmacotherapy of arterial hypertension. Aliskiren is the first in a new class of orally active, non-peptide, low molecular weight renin inhibitors, and so far the only renin inhibitor that has progressed to phase III clinical trials. This review summarizes the available data on the pharmacokinetic and pharmacodynamic properties of aliskiren and its clinical development for treatment of arterial hypertension.
肾素-血管紧张素-醛固酮系统(RAAS)在诸如高血压、充血性心力衰竭和慢性肾衰竭等疾病中的重要性早已得到认可。人们还证实,使用血管紧张素转换酶(ACE)抑制剂或血管紧张素II受体阻滞剂(ARB)抑制RAAS是干预这些疾病发病机制的有效方法。肾素抑制剂在最高水平、其源头阻断RAAS,因此可能为动脉高血压的药物治疗提供一种令人兴奋的新方法。阿利吉仑是新型口服活性、非肽类、低分子量肾素抑制剂中的首个药物,也是迄今为止唯一进入III期临床试验的肾素抑制剂。本综述总结了关于阿利吉仑药代动力学和药效学特性及其治疗动脉高血压临床进展的现有数据。