Henderson W R
University of Washington, Seattle.
Ann Allergy. 1994 Mar;72(3):272-8.
The allergen-induced release of leukotrienes, the 5-lipoxygenase products of arachidonic acid metabolism in activated airway cells, is critical in the pathophysiology of asthma. Key proteins in leukotriene formation are 5-lipoxygenase and 5-lipoxygenase-activating protein. The leukotrienes have potent biologic activity: leukotriene (LT)B4 is a chemoattractant for leukocytes and also induces leukocyte aggregation and adherence to vascular endothelium; and the sulfidopeptide leukotrienes, LTC4, LTD4, and LTE4 are bronchoconstrictors, induce airway mucous secretion, and increase vascular permeability. Sulfidopeptide leukotriene release has also been shown to be important in the pathogenesis of asthmatic aspirin intolerance. Effective, selective inhibitors of 5-lipoxygenase and 5-lipoxygenase-activating protein and leukotriene receptor antagonists have recently been developed as novel therapies for bronchial asthma and other inflammatory disorders.
在活化的气道细胞中,变应原诱导的白三烯释放是花生四烯酸代谢的5-脂氧合酶产物,在哮喘的病理生理学中起关键作用。白三烯形成中的关键蛋白是5-脂氧合酶和5-脂氧合酶激活蛋白。白三烯具有强大的生物活性:白三烯(LT)B4是白细胞的趋化因子,还可诱导白细胞聚集并黏附于血管内皮;而硫肽白三烯LTC4、LTD4和LTE4是支气管收缩剂,可诱导气道黏液分泌并增加血管通透性。硫肽白三烯的释放也已被证明在阿司匹林不耐受性哮喘的发病机制中起重要作用。最近已开发出有效的、选择性的5-脂氧合酶和5-脂氧合酶激活蛋白抑制剂以及白三烯受体拮抗剂,作为支气管哮喘和其他炎症性疾病的新型疗法。