Biology and Therapeutic Applications of Peroxisome Proliferator-Activated Receptors

被引:7
作者
Menendez-Gutierrez, Maria P. [1 ]
Roszer, Tamas [1 ]
Ricote, Mercedes [1 ]
机构
[1] CNIC, Cardiovasc Dev & Repair Dept, Madrid 28029, Spain
关键词
Nuclear receptors; PPAR; transcription; metabolism; inflammation; cardiovascular disease; neuroinflammation; cancer; GAMMA PPAR-GAMMA; HIGH-FAT DIET; NF-KAPPA-B; CAUSES INSULIN-RESISTANCE; ENDOTHELIAL GROWTH-FACTOR; HUMAN BREAST-CANCER; CELLS IN-VITRO; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; INHIBIT INFLAMMATORY RESPONSES; ALPHA AGONIST FENOFIBRATE;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Peroxisome proliferator-activated receptors (PPARs) are ligand dependent transcription factors. The three mammalian PPARs are key regulators of fatty acid and lipoprotein metabolism, glucose homeostasis, cellular proliferation/differentiation and the immune response. PPARs are therefore important targets in the treatment of metabolic disorders such as insulin resistance and type 2 diabetes mellitus, and are also of interest in relation to chronic inflammatory diseases such as atherosclerosis, arthritis, chronic pulmonary inflammation, pancreatitis, inflammatory bowel disease, and psoriasis. Recent advances have attributed novel functions to PPARs in blood pressure regulation, neuroinflammation, nerve-cell protection, inflammatory pain reduction, and the hypothalamic control of metabolism. The abundant pleiotropic actions of PPARs suggest that PPAR agonists have enormous therapeutic potential. However, current PPAR-based therapies often have undesired side effects due to the concomitant activation of PPARs in non-target cells. There is therefore growing interest in the development of cell-specific PPAR agonists and improvement of the clinical use of PPAR ligands. This review gives an overview of PPAR functions and discusses the current and potential medical implications of PPAR ligands in various pathologies, ranging from metabolic disorders to cardiovascular disease, chronic inflammation, neurodegenerative disorders and cancer.
引用
收藏
页码:548 / 584
页数:37
相关论文
共 436 条
[11]   An antidiabetic thiazolidinedione induces eccentric cardiac hypertrophy by cardiac volume overload in rats [J].
Arakawa, K ;
Ishihara, T ;
Aoto, M ;
Inamasu, M ;
Kitamura, K ;
Saito, A .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2004, 31 (1-2) :8-13
[12]   Free fatty acids repress the GLUT4 gene expression in cardiac muscle via novel response elements [J].
Armoni, M ;
Harel, C ;
Bar-Yoseph, F ;
Milo, S ;
Karnieli, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (41) :34786-34795
[13]   Peroxisome proliferator-activated receptor-γ represses GLUT4 promoter activity in primary adipocytes, and rosiglitazone alleviates this effect [J].
Armoni, M ;
Kritz, N ;
Harel, C ;
Bar-Yoseph, F ;
Chen, H ;
Quon, MJ ;
Karnieli, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (33) :30614-30623
[14]   Stimulatory Effects of Peroxisome Proliferator-Activated Receptor-γ on Fcγ Receptor-Mediated Phagocytosis by Alveolar Macrophages [J].
Aronoff, David M. ;
Serezani, Carlos H. ;
Carstens, Jennifer K. ;
Marshall, Teresa ;
Gangireddy, Srinivasa R. ;
Peters-Golden, Marc ;
Reddy, Raju C. .
PPAR RESEARCH, 2007, 2007
[15]   Peroxisome proliferator-activated receptor γ plays a critical role in inhibition of cardiac hypertrophy in vitro and in vivo [J].
Asakawa, M ;
Takano, H ;
Nagai, T ;
Uozumi, H ;
Hasegawa, H ;
Kubota, N ;
Saito, T ;
Masuda, Y ;
Kadowaki, T ;
Komuro, I .
CIRCULATION, 2002, 105 (10) :1240-1246
[16]   Expression of inducible 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase/PFKFB3 isoforms in adipocytes and their potential role in glycolytic regulation [J].
Atsumi, T ;
Nishio, T ;
Niwa, H ;
Takeuchi, J ;
Bando, H ;
Shimizu, C ;
Yoshioka, N ;
Bucala, R ;
Koike, T .
DIABETES, 2005, 54 (12) :3349-3357
[17]  
Atug O, 2008, J GASTROINTEST LIVER, V17, P433
[18]   Macrophage expression of peroxisome proliferator-activated receptor-α reduces atherosclerosis in low-density lipoprotein receptor-deficient mice [J].
Babaev, Vladimir R. ;
Ishiguro, Hiroyuki ;
Ding, Lei ;
Yancey, Patricia G. ;
Dove, Dwayne E. ;
Kovacs, William J. ;
Semenkovich, Clay F. ;
Fazio, Sergio ;
Linton, MacRae F. .
CIRCULATION, 2007, 116 (12) :1404-1412
[19]   Pleiotropic actions of fenofibrate on the heart [J].
Balakumar, Pitchai ;
Rohilla, Ankur ;
Mahadevan, Nanjaian .
PHARMACOLOGICAL RESEARCH, 2011, 63 (01) :8-12
[20]   PPAR dual agonists: Are they opening Pandora's box? [J].
Balakumar, Pitchal ;
Rose, Madhankumar ;
Ganti, Subrahmanya S. ;
Krishan, Pawan ;
Singh, Manjeet .
PHARMACOLOGICAL RESEARCH, 2007, 56 (02) :91-98