McMillan R M, Walker E R
Bioscience Department 1, ICI Pharmaceuticals, Macclesfield, Cheshire, UK.
Trends Pharmacol Sci. 1992 Aug;13(8):323-30. doi: 10.1016/0165-6147(92)90100-k.
Metabolism of arachidonic acid by the enzyme 5-lipoxygenase leads to the formation of a group of biologically active lipids known as leukotrienes. Peptidoleukotrienes are powerful bronchoconstrictor agents while leukotriene B4 is a potent chemotactic agent for a variety of leukocytes. In view of these properties, leukotrienes have been proposed as important mediators in allergic and inflammatory disorders, and inhibitors of 5-lipoxygenase, by blocking leukotriene synthesis, have therapeutic potential in a range of diseases including arthritis and asthma. This review by Rodger McMillan and Ed Walker summarizes the biology of leukotrienes and the current knowledge of the mechanism of 5-lipoxygenase, providing a framework for consideration of the discovery, development and clinical status of drugs in the three major classes of 5-lipoxygenase inhibitors: 'redox' inhibitors, iron ligand inhibitors and 'non-redox' inhibitors.
花生四烯酸经5-脂氧合酶代谢会生成一组被称为白三烯的生物活性脂质。肽白三烯是强效支气管收缩剂,而白三烯B4是多种白细胞的有效趋化剂。鉴于这些特性,白三烯被认为是过敏和炎症性疾病中的重要介质,而5-脂氧合酶抑制剂通过阻断白三烯的合成,在包括关节炎和哮喘在内的一系列疾病中具有治疗潜力。罗杰·麦克米兰和埃德·沃克撰写的这篇综述总结了白三烯的生物学特性以及目前对5-脂氧合酶作用机制的认识,为考量5-脂氧合酶抑制剂三大主要类别(“氧化还原”抑制剂、铁配体抑制剂和“非氧化还原”抑制剂)药物的发现、研发及临床状况提供了一个框架。