Bell R L, Lanni C, Malo P E, Brooks D W, Stewart A O, Hansen R, Rubin P, Carter G W
Ann N Y Acad Sci. 1993 Nov 30;696:205-15. doi: 10.1111/j.1749-6632.1993.tb17153.x.
The importance of leukotrienes as mediators of inflammation and bronchoconstriction was examined with two recently described 5-lipoxygenase inhibitors, zileuton and A-78773. Preclinical evaluation of these two molecules indicates that they are potent, selective, direct, reversible inhibitors of 5-lipoxygenase with activity in a variety of purified cells and in more complex biological systems such as whole blood, lung fragments, and tracheal tissues. In various animals models of inflammation and allergy, the molecules inhibited edema, inflammatory cell influx, and bronchospasm. These observations are consistent with the recent clinical success of zileuton in treating asthma and inflammatory bowel disease. In all preclinical systems tested thus far, A-78773 is more potent and longer acting than zileuton, indicating that the molecule could be even more effective in the clinic than zileuton and that both molecules are useful tools in defining the role of leukotrienes in preclinical and clinical settings.
利用最近描述的两种5-脂氧合酶抑制剂齐留通和A-78773,研究了白三烯作为炎症和支气管收缩介质的重要性。对这两种分子的临床前评估表明,它们是强效、选择性、直接、可逆的5-脂氧合酶抑制剂,在多种纯化细胞以及更复杂的生物系统(如全血、肺组织切片和气管组织)中均有活性。在各种炎症和过敏动物模型中,这些分子可抑制水肿、炎症细胞浸润和支气管痉挛。这些观察结果与齐留通最近在治疗哮喘和炎症性肠病方面的临床成功相一致。在迄今为止测试的所有临床前系统中,A-78773比齐留通更有效且作用时间更长,这表明该分子在临床上可能比齐留通更有效,并且这两种分子都是在临床前和临床环境中确定白三烯作用的有用工具。