PPARα as a therapeutic target in inflammation-associated diseases

被引:46
作者
Gervois, Philippe [1 ]
Mansouri, Roxane M. [1 ]
机构
[1] Univ Lille Nord France, Fac Sci Pharmaceut & Biol, Biochim Lab, F-59006 Lille, France
关键词
C/EBP; IL-1; IL-6; inflammation; NF-kappa B; PPAR alpha; STAT3; PROLIFERATOR-ACTIVATED-RECEPTOR; NF-KAPPA-B; TISSUE FACTOR EXPRESSION; CORONARY-HEART-DISEASE; C-REACTIVE PROTEIN; GENE-EXPRESSION; CARDIAC-HYPERTROPHY; TRANSCRIPTION FACTORS; AGONIST FENOFIBRATE; AIRWAY INFLAMMATION;
D O I
10.1517/14728222.2012.715633
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: The nuclear receptor peroxisome proliferator-activated receptor alpha (PPAR alpha) plays a major regulatory function of genes involved in energy metabolism and is a therapeutic target for dyslipidemia. The last decade provided a constellation of findings demonstrating that PPARa behaves as a modulator of both acute and chronic inflammation. PPARa became a rational potential therapeutic target for the treatment of inflammatory disorders. Aeras covered: The ability of PPARa to control inflammatory signaling pathways via a diversity of molecular mechanisms is discussed. This review is especially focused on the global action of PPARa on inflammation in several tissues from data obtained in numerous cell types and in vivo models exposed to inflammatory stimuli. Expert opinion: Available PPARa agonists currently used in clinic belong to the class of hypolipidemic drugs but were not expected and not designed to act as anti-inflammatory drugs. To date, accumulating preclinical suggest evidence promising benefits when considering PPARa as a drug target to treat inflammatory disorders. However, clinical studies are needed to validate this concept. Drug design should also be directed toward the elaboration of PPARa agonists more specifically active in the control inflammatory signaling.
引用
收藏
页码:1113 / 1125
页数:13
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