Department of Pharmacology, Ranbaxy Research Laboratories, Udyog Vihar, India.
Pharmacology. 2010;85(6):336-49. doi: 10.1159/000312669. Epub 2010 Jun 2.
The cysteinyl leukotrienes (CysLTs) are a family of potent inflammatory lipid mediators synthesized from arachidonic acid by a variety of cells including mast cells, eosinophils, basophils and macrophages. The family includes leukotriene C(4) (LTC(4)), leukotriene D(4) (LTD(4)) and leukotriene E(4) (LTE(4)), which are potent biological mediators in the pathophysiology of inflammatory diseases and trigger contractile and inflammatory processes through the specific interaction with cell surface receptors, belonging to the superfamily of G-protein-coupled receptor. Pharmacological characterizations have suggested the existence of at least 2 types of CysLT receptors based on potency of agonist and antagonist, designated as CysLT(1) and CysLT(2). The CysLT(1) receptors are mostly expressed in lung smooth muscle cells, interstitial lung macrophages and the spleen, and it has been studied a lot elucidating its role in the etiology of airway inflammation and asthma. On the other hand, CysLT(2) receptors are present in the heart, brain and adrenal glands. This review discusses the role of CysLTs and their receptor in the pathophysiology of various inflammatory disorders. The understanding of CysLTs and their receptors in allergic airway disease is currently limited to CysLT(1)-receptor-mediated effects, and the role of the CysLT(2) receptors is pharmacologically less well defined, as there is no specific antagonist available yet. Specific CysLT(2)-receptor-selective antagonists would be very helpful to identify the precise role of CysLT and their receptors. Some recent evidence indicates the existence of additional receptor subtypes and requires further investigation for a better understanding of the role of the CysLT receptors. This review is an effort to summarize the localization, regulation and expression pattern along with the molecular and functional pharmacology of the CysLT receptors and to discuss their role in the pathophysiology of different diseases along with the recent update.
半胱氨酰白三烯(CysLTs)是一类由花生四烯酸合成的强效炎症性脂质介质,由多种细胞产生,包括肥大细胞、嗜酸性粒细胞、嗜碱性粒细胞和巨噬细胞。该家族包括白三烯 C(4)(LTC(4))、白三烯 D(4)(LTD(4))和白三烯 E(4)(LTE(4)),它们是炎症性疾病病理生理学中的强效生物介质,通过与细胞表面受体的特异性相互作用引发收缩和炎症过程,属于 G 蛋白偶联受体超家族。药理学特性表明,至少存在 2 种类型的 CysLT 受体,根据激动剂和拮抗剂的效力,分别命名为 CysLT(1)和 CysLT(2)。CysLT(1)受体主要在肺平滑肌细胞、肺间质巨噬细胞和脾脏中表达,其在阐明气道炎症和哮喘发病机制中的作用已得到广泛研究。另一方面,CysLT(2)受体存在于心脏、大脑和肾上腺中。这篇综述讨论了 CysLTs 及其受体在各种炎症性疾病发病机制中的作用。目前,对 CysLTs 和 CysLT 受体在过敏性气道疾病中的作用的理解仅限于 CysLT(1)受体介导的作用,而 CysLT(2)受体的作用在药理学上定义得较少,因为目前还没有特定的拮抗剂可用。特异性 CysLT(2)受体选择性拮抗剂将非常有助于确定 CysLT 及其受体的确切作用。一些最近的证据表明存在其他受体亚型,需要进一步研究以更好地了解 CysLT 受体的作用。这篇综述旨在总结 CysLT 受体的定位、调节和表达模式以及分子和功能药理学,并讨论它们在不同疾病发病机制中的作用以及最近的更新。