Division of Diabetic Complications, Baker IDI Heart and Diabetes Institute, P.O. Box 6492, Melbourne, VIC 8008, Australia.
PPAR Res. 2012;2012:456529. doi: 10.1155/2012/456529. Epub 2012 Feb 12.
Pharmaceutical agonists of peroxisome proliferator-activated receptors (PPARs) are widely used in the management of type 2 diabetes, chiefly as lipid-lowering agents and oral hypoglycaemic agents. Although most of the focus has been placed on their cardiovascular effects, both positive and negative, these agents also have significant renoprotective actions in the diabetic kidney. Over and above action on metabolic control and effects on blood pressure, PPAR agonists also appear to have independent effects on a number of critical pathways that are implicated in the development and progression of diabetic kidney disease, including oxidative stress, inflammation, hypertrophy, and podocyte function. This review will examine these direct and indirect actions of PPAR agonists in the diabetic kidney and explore recent findings of clinical trials of PPAR agonists in patients with diabetes.
过氧化物酶体增殖物激活受体 (PPAR) 的药物激动剂被广泛用于 2 型糖尿病的治疗,主要用作降脂药和口服降糖药。尽管大多数研究都集中在其心血管作用上(既有积极的也有消极的),但这些药物在糖尿病肾脏中也具有显著的肾脏保护作用。除了对代谢控制的作用和对血压的影响外,PPAR 激动剂似乎还对许多与糖尿病肾病发生和进展有关的关键途径具有独立作用,包括氧化应激、炎症、肥大和足细胞功能。本文将探讨 PPAR 激动剂在糖尿病肾脏中的这些直接和间接作用,并探讨最近在糖尿病患者中进行的 PPAR 激动剂临床试验的结果。