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前列腺素合酶 1 和 2 及白三烯 C4 合酶在阿司匹林性哮喘中的表达作用:理论研究。

Role of expression of prostaglandin synthases 1 and 2 and leukotriene C4 synthase in aspirin-intolerant asthma: a theoretical study.

机构信息

Faculty of Natural Sciences and Mathematics, Faculty of Medicine, Faculty of Health Sciences, University of Maribor, Slomškov trg 15, 2000 Maribor, Slovenia.

出版信息

J Pharmacokinet Pharmacodyn. 2011 Apr;38(2):261-78. doi: 10.1007/s10928-011-9192-6. Epub 2011 Feb 18.

Abstract

Altered expressions of the key enzymes in arachidonic acid (AA) metabolism, prostaglandin synthase 1 and 2 and cysteinyl leukotriene C(4) synthase, are of importance in understanding aspirin-induced asthma. We propose a mathematical model of AA metabolism and its interaction with non-steroidal anti-inflammatory drugs (NSAIDs). Model simulations depict the impact of modified expressions of the above enzymes on the time dependent synthesis of cysteinyl leukotrienes and anti-inflammatory prostaglandins before and during NSAID exposure in different model states describing healthy humans as well as aspirin-tolerant and -intolerant asthmatics. The results are compared and evaluated with experimental data taken from the literature. Our results identify the decreased expression of prostaglandin H synthase 1 and increased expression of leukotriene C(4) synthase as the key elements in AA metabolism that contribute to increased leukotriene C(4) and decreased anti-inflammatory prostaglandins after NSAID dosing in aspirin-intolerant patients. On the other hand, the decreased expression of prostaglandin H synthase 2 implies permanently increased leukotriene C(4) and lowers the sensitivity to increased drug doses. The model is used for identification of susceptible patient populations for aspirin and ibuprofen, and for identification of critical aspirin doses that might induce bronchoconstriction.

摘要

花生四烯酸(AA)代谢中关键酶,前列腺素合酶 1 和 2 以及半胱氨酰白三烯 C(4)合酶的表达改变,对于理解阿司匹林诱发的哮喘非常重要。我们提出了一个 AA 代谢及其与非甾体抗炎药(NSAIDs)相互作用的数学模型。模型模拟描述了在不同模型状态下,健康人群以及阿司匹林耐受和不耐受哮喘患者中,上述酶的修饰表达对 NSAID 暴露前后时间依赖性半胱氨酰白三烯和抗炎前列腺素合成的影响。将结果与文献中的实验数据进行了比较和评估。我们的结果表明,前列腺素 H 合酶 1 的表达降低和白三烯 C(4)合酶的表达增加是 AA 代谢中的关键因素,导致阿司匹林不耐受患者 NSAID 给药后白三烯 C(4)增加和抗炎前列腺素减少。另一方面,前列腺素 H 合酶 2 的表达降低意味着永久性增加白三烯 C(4),并降低对增加药物剂量的敏感性。该模型用于鉴定阿司匹林和布洛芬易感患者人群,以及鉴定可能引起支气管收缩的关键阿司匹林剂量。

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