Protective Effects of Adiponectin Against Renal Ischemia-Reperfusion Injury Via Prostacyclin-PPARα-Heme Oxygenase-1 Signaling Pathway

被引:73
作者
Cheng, Ching-Feng [2 ,3 ,4 ]
Lian, Wei-Shiung [4 ,5 ]
Chen, Sung-Ho [1 ]
Lai, Pei-Fen [1 ]
Li, Hsiao-Fen [4 ]
Lan, Yi-Fan [1 ]
Cheng, Winston Teng-Kuei [6 ]
Lin, Heng [1 ,7 ]
机构
[1] Tzu Chi Univ, Inst Pharmacol & Toxicol, Coll Med, Hualien 970, Taiwan
[2] Tzu Chi Gen Hosp, Dept Med Res, Hualien, Taiwan
[3] Tzu Chi Univ, Dept Pediat, Hualien 970, Taiwan
[4] Acad Sinica, Inst Biomed Sci, Taipei, Taiwan
[5] Natl Taiwan Univ, Dept Anim Sci & Technol, Taipei 10764, Taiwan
[6] Tunghai Univ, Dept Anim Sci & Biotechnol, Taichung 40704, Taiwan
[7] Taipei Med Univ, Coll Med, Inst Physiol, Taipei, Taiwan
关键词
ACTIVATED PROTEIN-KINASE; FATTY-ACID OXIDATION; EPITHELIAL-CELLS; RECEPTOR-ALPHA; DIABETIC-RATS; EXPRESSION; KIDNEY; ADIPOSE; MUSCLE; INFLAMMATION;
D O I
10.1002/jcp.22726
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
Adiponectin (APN), a circulating adipose-derived hormone that regulates inflammation and energy metabolism, has beneficial effects on the cardiovascular disorders. Serum APN levels are lower in patients with coronary artery disease and higher in patients with chronic kidney disease. However, the precise role of APN in acute reno-vascular disease is not clear. Results of the present study show that serum APN concentration decreased after renal ischemia reperfusion (I/R) injury in mice. In addition, I/R-induced renal dysfunction (elevated serum creatinine and urea levels), inflammation (number of infiltrating neutrophils, myeloperoxidase activity), and apoptotic responses (apoptotic cell number and caspase-3 activation) were attenuated in APN-treated compared to control mice. Molecular and biochemical analysis revealed that APN up-regulates heme oxygenase-1 (HO-1) via peroxisome-proliferator-activated-receptor-alpha (PPAR alpha) dependent pathway which is mediated through the enhancement of COX-2 and 6-keto PGF1 alpha expression. Chromatin immune-precipitation assay demonstrated that APN increases the binding activity of PPAR alpha to PPRE region of HO-1 promoter. Furthermore, APN induced HO-1 expression was only found in wild-type but not in PPAR alpha gene deleted mice. This provides in vivo evidence that APN mediated HO-1 expression depends on PPAR alpha regulation. In conclusion, our results provide a novel APN mediated prostacyclin-PPAR alpha-HO-1 signaling pathway in protecting renal I/R injury. J. Cell. Physiol. 227: 239-249, 2012. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:239 / 249
页数:11
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