Aviram M, Brook J G
Prog Cardiovasc Dis. 1987 Jul-Aug;30(1):61-72. doi: 10.1016/0033-0620(87)90011-9.
Enhanced platelet activity in patients with hypercholesterolemia and moderate hypertriglyceridemia can be attributed to increased LDL and VLDL and/or decreased HDL concentrations. In marked hypertriglyceridemia, where there is an accumulation of chylomicrons, platelet function is reduced. Treatment, whether by diet, medication, or plasmapheresis, that will result in a change in lipoprotein pattern is accompanied by a parallel change in platelet responsiveness. Incubation of lipoproteins with isolated platelets results in enhancement of platelet activation by LDL and VLDL and suppression of activity by HDL and chylomicrons. These findings have in vivo confirmation. They are even more pronounced and sometimes altered when the lipoproteins are derived from hyperlipidemic subjects. The effects of the lipoproteins on platelet activity appear to be dependent on lipoprotein composition and on factors such as cholesterol:protein ratio, apo C-III0:apo C-III2 ratio, apo B concentration, and triglyceride:protein ratio. The lipoproteins interact with platelets at specific receptor sites. Rapid change in platelet composition, particularly with regard to cholesterol, phospholipid, and fatty acid content, might ensue, with consequent alterations in membrane fluidity and enzyme activities and either suppression or activation of platelet function. This review has indicated that lipoproteins have a clear influence on platelet function. This interaction could be well of paramount importance in determining atherogenic risk.
高胆固醇血症和中度高甘油三酯血症患者血小板活性增强可能归因于低密度脂蛋白(LDL)和极低密度脂蛋白(VLDL)增加及/或高密度脂蛋白(HDL)浓度降低。在明显的高甘油三酯血症中,由于乳糜微粒蓄积,血小板功能降低。通过饮食、药物或血浆置换进行的治疗,若能导致脂蛋白模式改变,会同时伴有血小板反应性的相应改变。将脂蛋白与分离的血小板一起孵育会导致LDL和VLDL增强血小板活化,而HDL和乳糜微粒则抑制其活性。这些发现已得到体内证实。当脂蛋白来自高脂血症患者时,这些作用更加明显,有时甚至会改变。脂蛋白对血小板活性的影响似乎取决于脂蛋白组成以及诸如胆固醇:蛋白质比率、载脂蛋白C-III0:载脂蛋白C-III2比率、载脂蛋白B浓度和甘油三酯:蛋白质比率等因素。脂蛋白在特定受体部位与血小板相互作用。血小板组成可能会迅速改变,尤其是在胆固醇、磷脂和脂肪酸含量方面,从而导致膜流动性和酶活性改变,进而抑制或激活血小板功能。本综述表明脂蛋白对血小板功能有明显影响。这种相互作用在确定动脉粥样硬化风险方面可能极为重要。