Antifibrotic Effects of Pioglitazone at Low Doses on the Diabetic Rat Kidney Are Associated with the Improvement of Markers of Cell Turnover, Tubular and Endothelial Integrity, and Angiogenesis

作者：Toblli Jorge E; Cao Gabriel; Giani Jorge F; Angerosa Margarita; Dominici Fernando P; Gonzalez Cadavid Nestor F^*

来源：Kidney & Blood Pressure Research, 2011, 34(1): 20-33.

DOI：10.1159/000320380

• Diabetic nephropathy
• Thiazolidinediones
• Peroxisome proliferator-activated receptor-gamma
• Metabolic syndrome
• Fibrosis
• Inflammation
• ZDF fa/fa rat
• Nitric oxide synthase
• VEGF
• Megalin

Background/Aims: Pioglitazone and other thiazolidinediones are renoprotective in diabetic nephropathy at doses that normalize glycemia, presumably as a consequence of glycennic control. However, low doses of pioglitazone that did not normalize glycemia in rat models of type 2 diabetes prevented tubulointerstitial fibrosis and glomerulosclerosis through counteracting inflammation, oxidative stress, cell cycle arrest, and fibrosis. The current work tested whether this low-dose treatment also reduces other fibrosis and inflammation factors in the diabetic kidney and prevents tubular cell loss, endothelial damage, and abnormal angiogenesis. Methods: ZDF fa/fa rats (ZDF) were fed for 4 months chow with 0.001% pioglitazone, and the untreated ZDF and the non-diabetic lean Zucker rats (LZR) received regular chow. Proteinuria, creatinine clearance, blood pressure, and renal quantitative histopathology markers were determined. Results: Correction of renal function in ZDF by pioglitazone, occurring with a glycemia >250 mg/dl, was accompanied by normalization of the renal levels of connective tissue growth factor and fibronectin (fibrosis), TNF-alpha, interleukin-6 and MCP-1 (inflammation), megalin (tubular cells), the PCNA/caspase-3 ratio (positive cell turnover), VEGF (abnormal angiogenesis), and the ratio between eNOS and iNOS (endothelial dysfunction). Conclusion:This supports mechanisms for the renoprotective effects of pioglitazone in diabetes additional to glycemic control.

• 出版日期2011