PPARγ as a therapeutic target in diabetic nephropathy and other renal diseases

被引:99
作者
Yang, Jichun [1 ]
Zhou, Yunfeng [1 ]
Guan, Youfei [1 ]
机构
[1] Peking Beijing Univ Hlth Sci Ctr, Dept Physiol & Pathophysiol, Peking Beijing Univ Diabet Ctr, Key Lab Mol Cardiovasc Sci, Beijing 100191, Peoples R China
关键词
diabetic nephropathy; hypertension; kidney injury; PPAR; ACTIVATED-RECEPTOR-GAMMA; GLYCATION END-PRODUCTS; TUBULAR EPITHELIAL-CELLS; CHRONIC KIDNEY-DISEASE; NF-KAPPA-B; INSULIN-RESISTANCE; MESANGIAL CELLS; ANGIOTENSIN-II; BLOOD-PRESSURE; ADIPONECTIN RECEPTORS;
D O I
10.1097/MNH.0b013e32834de526
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Purpose of review Peroxisome proliferator-activated receptor gamma (PPAR gamma) is a ligand-activated nuclear transcription factor that regulates many important physiological processes including glucose and lipid metabolism, energy homeostasis, cell proliferation, inflammation, immunity and reproduction. The current review aims to summarize and discuss recent findings evaluating the protective effects of PPAR gamma against kidney diseases with a focus on diabetic nephropathy. We will also delineate the potential underlying mechanisms. Recent findings PPAR gamma plays important roles in renal physiology and pathophysiology. Agonists of PPAR gamma exert protective effects against various kidney diseases including diabetic nephropathy, ischemic renal injury, IgA nephropathy, chemotherapy-associated kidney damage, polycystic kidney diseases and age-related kidney diseases via both systemic and renal actions. Summary PPAR gamma agonists are effective in delaying and even preventing the progression of many renal diseases, especially diabetic nephropathy. PPAR gamma may represent a promising target for the treatment of renal diseases.
引用
收藏
页码:97 / 105
页数:9
相关论文
共 128 条
[1]
A pilot randomized controlled trial of renal protection with pioglitazone in diabetic nephropathy [J].
Agarwal, R ;
Saha, C ;
Battiwala, M ;
Vasavada, N ;
Curley, T ;
Chase, SD ;
Sachs, N ;
Semret, MH .
KIDNEY INTERNATIONAL, 2005, 68 (01) :285-292
[2]
Fibrillogenic amylin evokes the apoptosis of human mesangial cells [J].
Ai, Peng ;
Zhi-Hong, Liu ;
Hong, Zhou ;
Mao-Yan, Zhu ;
Lei-Shi, Li .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2007, 78 (01) :16-22
[3]
The low dose combination of fenofibrate and rosiglitazone halts the progression of diabetes-induced experimental nephropathy [J].
Arora, Mandeep Kumar ;
Reddy, Krishna ;
Balakumar, Pitchai .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2010, 636 (1-3) :137-144
[4]
Telmisartan prevents the progression of renal injury in daunorubicin rats with the alteration of angiotensin II and endothelin-1 receptor expression associated with its PPAR-γ agonist actions [J].
Arozal, Wawaimuli ;
Watanabe, Kenichi ;
Veeraveedu, Punniyakoti T. ;
Ma, Meilei ;
Thandavarayan, Rajarajan A. ;
Sukumaran, Vijayakumar ;
Suzuki, Kenji ;
Kodama, Makoto ;
Aizawa, Yoshifusa .
TOXICOLOGY, 2011, 279 (1-3) :91-99
[5]
The lack of cyclin kinase inhibitor p27Kip1 ameliorates progression of diabetic nephropathy [J].
Awazu, M ;
Omori, S ;
Ishikura, K ;
Hida, M ;
Fujita, H .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (03) :699-708
[6]
PPAR ligands: Are they potential agents for cardiovascular disorders? [J].
Balakumar, Pitchai ;
Rose, Madhankumar ;
Singh, Manjeet .
PHARMACOLOGY, 2007, 80 (01) :1-10
[7]
Emerging role of PPAR ligands in the management of diabetic nephropathy [J].
Balakumar, Pitchai ;
Arora, Mandeep Kumar ;
Singh, Manjeet .
PHARMACOLOGICAL RESEARCH, 2009, 60 (03) :170-173
[8]
Blazer-Yost BL, 2010, PPAR RES, V2010, DOI [10.1155/2010/785369, 10.1155/2010/274376]
[9]
Advanced glycation end-products and the kidney [J].
Busch, Martin ;
Franke, Sybille ;
Ruester, Christiane ;
Wolf, Gunter .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2010, 40 (08) :742-755
[10]
Adiponectin stimulates phosphorylation of AMP-activated protein kinase α in renal glomeruli [J].
Cammisotto, Philippe G. ;
Bendayan, Moise .
JOURNAL OF MOLECULAR HISTOLOGY, 2008, 39 (06) :579-584