Division of Nephrology and Hypertension, Oregon Health & Science University, Portland, OR 97239-2940, USA.
Curr Diab Rep. 2009 Dec;9(6):447-52. doi: 10.1007/s11892-009-0073-y.
Inhibition of the renin-angiotensin-aldosterone system (RAAS) plays a pivotal role in preventing and treating diabetic nephropathy. However, despite documented beneficial effects of RAAS inhibitors in diabetic patients with nephropathy, reversal of the progressive course of this disorder or at least long-term stabilization of renal function are often difficult to achieve, and many patients still progress to end-stage renal disease. Incomplete inhibition of the RAAS has been postulated as one of the reasons for unsatisfactory therapeutic responses to RAAS inhibition in some patients. Inhibition of renin, a rate-limiting step in the RAAS activation cascade, is the logical approach to overcome at least some of the above-mentioned problems associated with the treatment with traditional RAAS inhibitors. This article focuses on experimental and clinical studies evaluating the two principal approaches to renin inhibition: direct renin inhibition with competitive inhibitors (eg, aliskiren) and inhibition of the (pro)renin receptor.
肾素-血管紧张素-醛固酮系统(RAAS)的抑制在预防和治疗糖尿病肾病方面起着关键作用。然而,尽管有文献证明 RAAS 抑制剂对合并肾病的糖尿病患者有益,但该疾病的进行性过程的逆转,或至少肾功能的长期稳定,往往难以实现,许多患者仍会进展为终末期肾病。RAAS 抑制不完全被认为是一些患者对 RAAS 抑制治疗反应不佳的原因之一。RAAS 激活级联反应中的限速步骤——肾素的抑制,是克服与传统 RAAS 抑制剂治疗相关的至少部分上述问题的合理方法。本文重点介绍了评估两种主要肾素抑制方法的实验和临床研究:竞争性抑制剂(如阿利克仑)的直接肾素抑制和(前)肾素受体的抑制。