Department of Internal Medicine, Korea University Ansan-Hospital, 516 Kojan-Dong, Ansan City, Kyungki-Do 425-020, Korea.
Curr Diab Rep. 2009 Dec;9(6):453-9. doi: 10.1007/s11892-009-0074-x.
Aldosterone plays an important role in salt and water homeostasis and blood pressure control through the classical mineralocorticoid receptor. However, recent findings of the mineralocorticoid receptor in nonepithelial tissues suggest that aldosterone may have additional functions. Significant evidence now exists suggesting that aldosterone directly induces tissue injury. Systemic or local aldosterone has emerged as a multifunctional hormone exhibiting profibrotic and proinflammatory actions that extend beyond the classical hemodynamic effect. The incomplete blockade of the renin-angiotensin-aldosterone system by angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers has led to experimental and clinical efforts using aldosterone inhibition. Recently, these efforts have provided us with an expanded understanding of a new pathogenic role for aldosterone in diabetic vascular complications. This article focuses on the role of aldosterone in the pathogenesis of diabetic kidney disease and recent important clinical data supporting the inhibition of aldosterone in treating diabetic kidney disease.
醛固酮通过经典的盐皮质激素受体在盐和水稳态及血压控制中发挥重要作用。然而,最近在非上皮组织中发现的盐皮质激素受体表明,醛固酮可能具有额外的功能。现在有大量证据表明,醛固酮可直接诱导组织损伤。全身性或局部醛固酮已成为一种多功能激素,具有成纤维和促炎作用,超出了经典的血流动力学效应。血管紧张素转换酶抑制剂或血管紧张素 II 受体阻滞剂对肾素-血管紧张素-醛固酮系统的不完全阻断导致了使用醛固酮抑制的实验和临床研究。最近,这些研究使我们对醛固酮在糖尿病血管并发症中的新致病作用有了更广泛的认识。本文重点介绍醛固酮在糖尿病肾病发病机制中的作用以及支持醛固酮抑制治疗糖尿病肾病的最新重要临床数据。