Steinhilber D
Institute of Pharmaceutical Chemistry, University of Frankfurt Marie-Curie-Str. 9 Frankfurt D-60439 Germany.
Curr Med Chem. 1999 Jan;6(1):71-85.
Arachidonate 5-lipoxygenase is the key enzyme in leukotriene biosynthesis and catalyzes the initial steps in the conversion of arachidonic acid to biologically active leukotrienes. Leukotrienes are considered as potent potent mediators of inflammatory and allergic reactions which are locally released by leukocytes and other 5-LO expressing cells and exert their effects via binding to specific membrane receptors and, as suggested recently, the nuclear receptor PPARa. Because of the proinflammatory profile of leukotrienes it was assumed that leukotriene biosynthesis inhibitors and leukotriene receptor antagonists have a therapeutical potential in a variety of inflammatory diseases. Clinical studies confirmed the therapeutic value of the antileukotriene therapy in asthma but the results with leukotriene biosynthesis inhibitors in psoriasis, arthritis and inflammatory bowel disease were more or less disappointing. This review summarizes the biochemistry of the 5-lipoxygenase pathway, the pharmacology of FLAP and 5 lipoxygenase inhibitors and discusses possible criteria for the development of these drugs.
花生四烯酸5-脂氧合酶是白三烯生物合成中的关键酶,催化花生四烯酸转化为生物活性白三烯的起始步骤。白三烯被认为是炎症和过敏反应的强效介质,由白细胞和其他表达5-脂氧合酶的细胞在局部释放,并通过与特定膜受体结合发挥作用,最近还发现其可与核受体PPARα结合发挥作用。由于白三烯具有促炎特性,人们认为白三烯生物合成抑制剂和白三烯受体拮抗剂在多种炎症性疾病中具有治疗潜力。临床研究证实了抗白三烯疗法在哮喘治疗中的价值,但白三烯生物合成抑制剂在银屑病、关节炎和炎症性肠病中的治疗效果或多或少令人失望。本综述总结了5-脂氧合酶途径的生物化学、FLAP和5-脂氧合酶抑制剂的药理学,并讨论了这些药物开发的可能标准。