Devillier P, Baccard N, Advenier C
Laboratoire de Pharmacologie et Toxicologie, Ho@a5pital Maison Blanche, Centre Hospitalier et Universitaire de Reims, 45, rue Cognacq Jay, Reims, Cedex, 51092, France.
Pharmacol Res. 1999 Jul;40(1):3-13. doi: 10.1006/phrs.1998.0458.
Asthma is a chronic inflammatory disease associated with airflow obstruction. Airflow obstruction results from contraction of airway smooth muscle, mucosal oedema, increased secretion of mucus and infiltration of the airway wall by inflammatory cells, particularly eosinophils. Leukotrienes are thought to contribute to the pathophysiology of asthma. Leukotrienes are synthesised from arachidonic acid by a specific synthesis pathway whose key enzyme is 5-lipoxygenase. Cysteinyl leukotrienes (leukotrienes C4, D4 and E4) have been shown to mimic all the pathologic changes that are characteristic of asthma, whereas leukotriene B4 does not appear to exert biological properties relevant to asthma. Cysteinyl leukotrienes bind to two receptor subtypes: CysLT1 and CysLT2. Most of the biological properties of cysteinyl leukotrienes relevant to asthma are mediated through CysLT1 receptor stimulation.
哮喘是一种与气流阻塞相关的慢性炎症性疾病。气流阻塞是由气道平滑肌收缩、黏膜水肿、黏液分泌增加以及炎症细胞(特别是嗜酸性粒细胞)浸润气道壁所致。白三烯被认为与哮喘的病理生理学有关。白三烯是由花生四烯酸通过特定的合成途径合成的,该途径的关键酶是5-脂氧合酶。半胱氨酰白三烯(白三烯C4、D4和E4)已被证明可模拟哮喘的所有特征性病理变化,而白三烯B4似乎不具有与哮喘相关的生物学特性。半胱氨酰白三烯与两种受体亚型结合:CysLT1和CysLT2。与哮喘相关的半胱氨酰白三烯的大多数生物学特性是通过刺激CysLT1受体介导的。