Pioglitazone Improves Obesity Type Diabetic Nephropathy: Relation to the Mitigation of Renal Oxidative Reaction

作者：Hirasawa Yasushi^*; Matsui Yukari; Yamane Kazusuke; Yabuki Shin ya; Kawasaki Yukiko; Toyoshi Tohru; Kyuki Kohei; Ito Masanori; Sakai Takayuki; Nagamatsu Tadashi

来源：Experimental Animals, 2008, 57(5): 423-432.

DOI：10.1538/expanim.57.423

• 8-hydroxydeoxyguanosine (8-OHdG)
• malondialdehyde (MDA)
• pioglitazone
• receptor for advanced glycation end-products (RAGE)
• transforming growth factor-beta (TGF-beta)

Medications to treat hyperglycemia and hyperinsulinemia are expected to inhibit the accumulation of advanced glycation end-products in the diabetic kidney and improve renal function by inhibiting oxidative reactions. In this study, we examined the effect of pioglitazone, an insulin sensitizer, on diabetic nephropathy. Feed containing pioglitazone at 0.01 or 0.02% was given to Zucker-fatty rats for 27 weeks. Pioglitazone reduced plasma glucose, plasma insulin, and blood HbAlc levels. It also decreased plasma total cholesterol, triglyceride, phospholipid and cystatin C levels and inhibited the increase in urine of 8-hydroxydeoxyguanosine and in plasma of malondialdehyde. In the histopathological examinations, pioglitazone inhibited diffusive or nodular thickening of the mesangial matrix, atrophy of the proximal convoluted tubule, thickening of the basement membrane of the tubule, and mild cellular infiltration (mostly small lymphocytes) in the stroma. Furthermore, pioglitazone inhibited the mRNA expression of the receptor for advanced glycation end-products (RAGE) and that of transforming growth factor-beta. Long-term administration of pioglitazone improved hyperglycemia lipid profiles, hypercholesterolemia, and hyperinsulinemia and had a protective effect on diabetic nephropathy in Zucker-fatty rats.

• 出版日期2008-10