Korotaeva Aleksandra A, Samoilova Elena V, Kaminny Aleksander I, Pirkova Aleksandra A, Resink Therese J, Erne Paul, Prokazova Nina V, Tkachuk Vsevolod A, Chazov Evgeny I
Cardiology Research Center, Moscow, Russia.
Mol Cell Biochem. 2005 Feb;270(1-2):107-13. doi: 10.1007/s11010-005-5266-3.
Secretory phospholipase A2 type IIA (sPLA2) may actively contribute to atherogenesis, acting either within the arterial wall or in plasma. Proinflammatory eicosanoids and lysophospholipids, generated through hydrolysis of cell membrane phospho-lipids by sPLA2, initiate and prolong the inflammatory process. In the present study we examined the possible involvement of sPLA2 in development of restenosis in patients undergoing percutaneous transluminal coronary angioplasty (PTCA). We also investigated whether serum sPLA2 could catalyze accumulation of lysophosphatidylcholine (LPC) in LDL. Concentrations and catalytic activities of sPLA2 were measured in blood serum of 49 consenting patients immediately before, 1-7 and 180 days after PTCA. All patients had repeat angiograms at 180-day follow-up. Restenosis was registered in 19 patients. Accumulation of LPC in LDL was evaluated by thin-layer chromatography after incubation of blood serum with LDL. Serum sPLA2 concentrations increased in all study patients by day 1 post-PTCA, but the increase was significantly greater and more protracted in patients who developed restenosis. Catalytic activities increased significantly 6 days post-PTCA in patients who developed restenosis, whereas for patients without restenosis there was no change in serum sPLA2 activity throughout the study period in spite of the sPLA2 presence in blood. Incubation of blood serum (6 days post-PTCA) with LDL resulted in accumulation of LPC only for those patients who subsequently developed restenosis. Manoalide, a specific inhibitor of sPLA2, completely blocked the LPC accumulation. The data indicate that elevated serum sPLA2 activity after PTCA is associated with restenosis development and may be involved in atherogenic modification of LDL in blood serum.
IIA型分泌型磷脂酶A2(sPLA2)可能通过在动脉壁内或血浆中发挥作用,积极促进动脉粥样硬化的发生。sPLA2通过水解细胞膜磷脂产生的促炎类二十烷酸和溶血磷脂,启动并延长炎症过程。在本研究中,我们研究了sPLA2在接受经皮腔内冠状动脉成形术(PTCA)的患者再狭窄发展过程中可能发挥的作用。我们还研究了血清sPLA2是否能催化低密度脂蛋白(LDL)中溶血磷脂酰胆碱(LPC)的积累。在49名同意参与研究的患者PTCA术前、术后1 - 7天和180天时,测定其血清中sPLA2的浓度和催化活性。所有患者在180天随访时均进行了重复血管造影。19名患者出现了再狭窄。通过将血清与LDL孵育后,用薄层色谱法评估LDL中LPC的积累情况。所有研究患者在PTCA术后第1天血清sPLA2浓度均升高,但再狭窄患者的升高幅度更大且持续时间更长。发生再狭窄的患者在PTCA术后6天催化活性显著增加,而未发生再狭窄的患者在整个研究期间血清sPLA2活性无变化,尽管血液中存在sPLA2。将PTCA术后6天的血清与LDL孵育,仅在那些随后发生再狭窄的患者中导致了LPC的积累。sPLA2的特异性抑制剂 manoalide完全阻断了LPC的积累。数据表明,PTCA术后血清sPLA2活性升高与再狭窄的发生有关,并且可能参与血清中LDL的动脉粥样硬化修饰。