SUNY Downstate Medical Center, 450 Clarkson Avenue, Box 1205, Brooklyn, NY 11203, USA.
Curr Cardiol Rep. 2009 Nov;11(6):445-51. doi: 10.1007/s11886-009-0064-2.
Secretory phospholipase A(2) (sPLA(2)) represents a class of enzymes that hydrolyze phospholipids from cellular membranes and lipoproteins, resulting in multifarious proatherogenic actions in the vessel wall. Proatherogenic actions of sPLA(2) involve lipoprotein remodeling that facilitates proteoglycan binding and formation of lipid aggregates that are rapidly internalized by tissue macrophages. The hydrolysis of phospholipids on cell membranes generates bioactive lipids and lipolipoproteins with increased oxidative susceptibility. These particles and other bioactive lipids activate inflammatory pathways in various cells of the vessel wall. Transgenic mice overexpressing groups IIA, V, and X have increased atherosclerosis formation, whereas mice deficient in these sPLA(2) isoenzymes have less atherosclerosis formation. In apolipoprotein E knockout mice fed an atherosclerotic diet, sPLA(2) inhibition with varespladib reduced atherosclerosis formation. The potential for sPLA(2) inhibitors for preventing cardiovascular events is being investigated.
分泌型磷脂酶 A(2)(sPLA(2))代表了一类能够从细胞膜和脂蛋白中水解磷脂的酶,在血管壁中产生多种促动脉粥样硬化作用。sPLA(2)的促动脉粥样硬化作用涉及脂蛋白重塑,促进了与蛋白聚糖的结合以及脂质聚集体的形成,这些聚集体被组织巨噬细胞迅速内化。细胞膜上的磷脂水解生成具有增加的氧化易感性的生物活性脂质和脂蛋白。这些颗粒和其他生物活性脂质激活血管壁中各种细胞的炎症途径。过表达 IIA、V 和 X 组的转基因小鼠形成动脉粥样硬化增加,而这些 sPLA(2)同工酶缺乏的小鼠形成的动脉粥样硬化减少。在喂食动脉粥样硬化饮食的载脂蛋白 E 基因敲除小鼠中,用 varespladib 抑制 sPLA(2)可减少动脉粥样硬化形成。正在研究 sPLA(2)抑制剂预防心血管事件的潜力。