Metformin prevents renal interstitial fibrosis in mice with unilateral ureteral obstruction

被引:62
作者
Cavaglieri, Rita C. [1 ]
Day, Robert T. [1 ]
Feliers, Denis [1 ]
Abboud, Hanna E. [1 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Med Nephrol, San Antonio, TX 78229 USA
关键词
Metformin; Adenosine monophosphate-activated kinase; Kidney; Fibrosis; Inflammation; ACTIVATED PROTEIN-KINASE; CHRONIC KIDNEY-DISEASE; TUBULOINTERSTITIAL FIBROSIS; CARDIAC FIBROSIS; NEPHROPATHY; PROGRESSION; EXPRESSION; MODEL; AMPK; MECHANISMS;
D O I
10.1016/j.mce.2015.06.006
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Unilateral ureteral obstruction causes important tubulo-interstitial fibrosis in the kidney. Metformin reduces fibrosis in mice with diabetic nephropathy. We examined the effects of metformin in a mouse model of unilateral ureteral obstruction (UUO). Expression of inflammation and fibrosis markers was studied by immunohistochemistry, immunoblot and quantitative real-time polymerase chain reaction. Seven days after UUO, kidneys presented dilated tubules, expansion of the tubulo-interstitial compartment, and significant infiltration of inflammatory cells. Macrophage infiltration and inflammation markers expression were increased in obstructed kidneys and reduced by metformin. Metformin reduced expression of extracellular matrix proteins and profibrotic factor TGF beta in obstructed kidneys, measured by immunohistochemistry. Interstitial fibroblast activation was evident in obstructed kidneys and ameliorated by metformin. UUO did not affect adenosine monophosphate-activated kinase (AMPK) activity, but metformin activated AMPK. Our results show that metformin prevents or slows down the onset of renal inflammation and fibrosis in mice with UUO, an effect that could be mediated by activation of AMPK. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:116 / 122
页数:7
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