Greenwood John, Mason Justin C
Department of Cell Biology, Institute of Ophthalmology, University College London, London EC1V 9EL, UK.
Trends Immunol. 2007 Feb;28(2):88-98. doi: 10.1016/j.it.2006.12.003. Epub 2007 Jan 2.
Statins reduce cholesterol synthesis and are widely used for the treatment of hyperlipidaemia and ischaemic heart disease. Besides their cholesterol-lowering effects, statins also possess broad immunomodulatory and anti-inflammatory properties. Vascular endothelial cells have a crucial role in the pathogenesis of inflammatory disease, and, alongside leukocytes and antigen-presenting cells, represent a key cellular target for statin therapy. Recent studies investigating how these drugs modify endothelial cell function demonstrate that the therapeutic effect of statins can be attributed, in part, to their action on the endothelium. Accordingly, statins attenuate endothelial MHC class II expression, increase endothelial nitric oxide synthase and fibrinolytic activity, decrease leukocyte adhesion and transmigration, and enhance resistance to local injurious stimuli. Many of these effects are brought about by the modulation of small GTPase function and the downregulation of proinflammatory gene expression.
他汀类药物可降低胆固醇合成,广泛用于治疗高脂血症和缺血性心脏病。除了降胆固醇作用外,他汀类药物还具有广泛的免疫调节和抗炎特性。血管内皮细胞在炎症性疾病的发病机制中起关键作用,与白细胞和抗原呈递细胞一起,是他汀类药物治疗的关键细胞靶点。最近关于这些药物如何改变内皮细胞功能的研究表明,他汀类药物的治疗效果部分可归因于它们对内皮的作用。因此,他汀类药物可减弱内皮细胞II类主要组织相容性复合体表达,增加内皮型一氧化氮合酶和纤溶活性,减少白细胞黏附和迁移,并增强对局部损伤刺激的抵抗力。这些作用许多是通过调节小GTP酶功能和下调促炎基因表达实现的。