Targeting leukotriene B4 in inflammation

被引:40
作者
Di Gennaro, Antonio [1 ]
Haeggstrom, Jesper Z. [1 ]
机构
[1] Karolinska Inst, Dept Med Biochem & Biophys, Div Chem 2, S-17177 Stockholm, Sweden
关键词
5-lipoxygenase; arachidonic acid; inflammatory diseases; leukotriene A(4) hydrolase; CYTOSOLIC PHOSPHOLIPASE A(2); ISCHEMIA-REPERFUSION INJURY; COLLAGEN-INDUCED ARTHRITIS; A(4) HYDROLASE INHIBITOR; 5-LIPOXYGENASE PATHWAY; ARACHIDONIC-ACID; RECEPTOR BLT1; IN-VIVO; T-CELLS; POLYMORPHONUCLEAR LEUKOCYTES;
D O I
10.1517/14728222.2013.843671
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Leukotriene (LT) B-4 is a powerful proinflammatory lipid mediator and triggers adherence to the endothelium, activates and recruits leukocytes to the site of injury. When formed in excess, LTB4 plays a pathogenic role and may sustain chronic inflammation in diseases such as asthma, rheumatoid arthritis, and inflammatory bowel disease. Recent investigations have also indicated that LTB4 is involved in cardiovascular diseases. Areas covered: As the 5-lipoxygenase pathway involves several discrete, tightly coupled, enzymes, which convert the substrate, 'step by step', into bioactive products, several different strategies have been used to target LTB4 as a means to treat inflammation. Here, we discuss recent findings regarding the development of selective enzyme inhibitors and antagonists for LTB4 receptors, as well as their application in preclinical and clinical studies. Expert opinion: Components of the 5-lipoxygenase pathway have received considerable attention as candidate drug targets resulting in one new class of medications against asthma, that is, the antileukotrienes. However, efforts to specifically target LTB4 have not yet been fruitful in the clinical setting, in spite of very promising preclinical data. Recently, crystal structures along with hitherto unknown functions of key enzymes in the leukotriene cascade have emerged, offering new opportunities for drug development and, with time, pharmacological intervention in LTB4-mediated pathologies.
引用
收藏
页码:79 / 93
页数:15
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