Lever R, Hefni A, Moffatt J D, Paul W, Page C P
Department of Pharmacology, The School of Pharmacy, 29-39 Brunswick Square, London, UK.
Clin Exp Allergy. 2007 Jun;37(6):909-17. doi: 10.1111/j.1365-2222.2007.02730.x.
Tecastemizole, a major metabolite of astemizole, is a potent and selective H1 receptor antagonist. Evidence suggests that this and certain other H1 receptor antagonists may possess anti-inflammatory effects that are, in some cases, independent of H1 receptor antagonism. Objective The aim of this study was to investigate the anti-inflammatory effects of tectastemizole in models of allergic inflammation.
Effects of tecastemizole were assessed in a murine model of allergic lung inflammation, in passive cutaneous anaphylaxis (PCA) responses in guinea-pig skin and in in vitro assays measuring endothelial adhesion molecule expression and leucocyte-endothelial adhesion.
Tecastemizole inhibited antigen-induced eosinophil recruitment to the lungs of allergic mice in a dose-dependent manner. Furthermore, combination of a sub-effective dose of tecastemizole, combined with a sub-effective dose of dexamethasone inhibited eosinophil accumulation in this model. Plasma extravasation in PCA reactions was inhibited by tecastemizole, although by a mechanism that would appear to be H1 receptor-dependent. Cytokine-induced endothelial intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 expression, as well as mononuclear cell adhesion to human umbilical vein endothelial cells was inhibited by tecastemazole in a manner independent of H1 receptor antagonism.
These data suggest that tecastemizole may have H1 receptor-independent effects in inhibiting late-phase inflammatory responses, while acute responses appear to be inhibited in a H1 receptor-dependent manner. Furthermore, our data suggest an important potential steroid-sparing role for such drugs in the treatment of allergic inflammatory conditions.
特卡司咪唑是阿司咪唑的主要代谢产物,是一种强效且选择性的H1受体拮抗剂。有证据表明,这种药物以及某些其他H1受体拮抗剂可能具有抗炎作用,在某些情况下,这些抗炎作用独立于H1受体拮抗作用。目的:本研究旨在探讨特卡司咪唑在变应性炎症模型中的抗炎作用。
在小鼠变应性肺炎症模型、豚鼠皮肤被动皮肤过敏反应(PCA)以及测量内皮细胞黏附分子表达和白细胞-内皮细胞黏附的体外试验中评估特卡司咪唑的作用。
特卡司咪唑以剂量依赖的方式抑制变应性小鼠肺部抗原诱导的嗜酸性粒细胞募集。此外,亚有效剂量的特卡司咪唑与亚有效剂量的地塞米松联合使用可抑制该模型中嗜酸性粒细胞的聚集。特卡司咪唑可抑制PCA反应中的血浆渗出,尽管其机制似乎依赖于H1受体。特卡司咪唑以独立于H1受体拮抗作用的方式抑制细胞因子诱导的内皮细胞细胞间黏附分子-1和血管细胞黏附分子-1表达,以及单核细胞与人脐静脉内皮细胞的黏附。
这些数据表明,特卡司咪唑在抑制晚期炎症反应方面可能具有不依赖于H1受体的作用,而急性反应似乎以依赖于H1受体的方式被抑制。此外,我们的数据表明这类药物在变应性炎症性疾病的治疗中可能具有重要的潜在节省类固醇作用。