Prolonged Administration Enhances the Renoprotective Effect of Pentoxifylline via Anti-Inflammatory Activity in Streptozotocin-Induced Diabetic Nephropathy

被引:21
|
作者
Han, Kum Hyun [1 ]
Han, Sang Youb [1 ]
Kim, Han Seong [2 ]
Kang, Young Sun [3 ]
Cha, Dae Ryong [3 ]
机构
[1] Inje Univ, Ilsan Paik Hosp, Dept Internal Med, Coll Med, Goyang 411706, Gyeonggi Prov, South Korea
[2] Inje Univ, Ilsan Paik Hosp, Dept Pathol, Coll Med, Goyang 411706, Gyeonggi Prov, South Korea
[3] Korea Univ, Dept Internal Med, Coll Med, Ansan Hosp, Ansan, South Korea
关键词
diabetic nephropathy; inflammation; pentoxifylline; MONOCYTE CHEMOATTRACTANT PROTEIN-1; CONVERTING ENZYME-INHIBITION; TUMOR-NECROSIS-FACTOR; GENE-THERAPY; SHORT-TERM; URINARY; PROGRESSION; EXPRESSION; EXCRETION; BLOCKADE;
D O I
10.1007/s10753-009-9167-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The beneficial effects of pentoxifylline (PTX), which has an anti-inflammatory and renoprotective effect in diabetic nephropathy, are not completely understood. This study investigates whether prolonged administration of PTX (40 mg/kg, per oral) is effective in streptozotocin-induced diabetic nephropathy. The amount of urinary protein was higher in the diabetic rats than in the control rats. The amount remained unchanged after 4 weeks and decreased after 8 weeks of PTX treatment. Accumulation of monocyte chemoattractant peptide-1 (MCP-1) and mouse monoclonal anti-monocyte/macrophage antibody (ED-1) positive cells was higher in untreated diabetic rats than in the control rats. PTX administration ameliorated the urinary MCP-1 excretion and interstitial infiltration of ED-1 positive cells at 4 weeks. Further, in diabetic rats, administration of PTX for 4 weeks inhibited the renal inflammatory reaction, and when administration for 8 weeks, it prevented proteinuria. These findings support the hypothesis that prolonged administration enhances the protective effects of PTX.
引用
收藏
页码:137 / 143
页数:7
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