White J G, Rao G H, Gerrard J M
Am J Pathol. 1977 Aug;88(2):387-402.
All agents capable of triggering the platelet release reaction also stimulate prostaglandin biosynthesis in these cells. Information concerning the endoperoxides, thromboxanes, and more stable metabolites generated by the action of cyclooxygenase and lipoxygenase on arachidonic acid has accumulated rapidly, but little is known about the preliminary steps in the cleavage and preparation of arachidonic acid for insertion into the enzymatic pathways of prostaglandin synthesis. Studies in this laboratory have shown that the combination of nitroblue tetrazolium (NBT) and vitamin E which prevents oxygenation of arachidonic acid to a free radical also blocks platelet prostaglandin biosynthesis. The present study has evaluated the influence of NBT, vitamin E, and the combination of NBT and vitamin E on the fine structure and biochemistry of platelets during incubation, and the effects of these compounds on the aggregation and secretion of platelets stimulated by collagen, thrombin, epinephrine, and ADP. Results of the study demonstrate that NBT and vitamin E, rather than injuring platelets, appear to protect them during incubation. Together NBT and vitamin E blocked aggregation by epinephrine, collagen, and thrombin, but permitted a small first wave stimulated by ADP. Both ADP and thrombin induced shape change, pseudopod formation, and limited degrees of internal contraction in vitamin E-NBT-treated platelets, whereas epinephrine and collagen failed to significantly alter discoid form. This pattern of response to aggregating agents was identical to reactions observed in platelets pretreated with aspirin and indomethacin, both potent inhibitors of platelet prostaglandin synthesis. In addition, NBT-vitamin E virtually blocked the first wave of aggregation which is not affected by aspirin and indomethacin. The findings support the concept that conversion of arachidonic acid to an activated state is an important step in prostaglandin synthesis and that electron transfer or oxidation-reduction reactions are intimately involved in the development of platelet stickiness.
所有能够引发血小板释放反应的介质也会刺激这些细胞中的前列腺素生物合成。关于环氧化酶和脂氧合酶作用于花生四烯酸所产生的内过氧化物、血栓烷以及更稳定的代谢产物的信息迅速积累,但对于花生四烯酸裂解和准备插入前列腺素合成酶促途径的初步步骤却知之甚少。本实验室的研究表明,硝基蓝四唑(NBT)和维生素E的组合可防止花生四烯酸氧化为自由基,同时也会阻断血小板前列腺素的生物合成。本研究评估了NBT、维生素E以及NBT与维生素E的组合在孵育过程中对血小板精细结构和生物化学的影响,以及这些化合物对胶原蛋白、凝血酶、肾上腺素和ADP刺激的血小板聚集和分泌的影响。研究结果表明,NBT和维生素E在孵育过程中似乎是保护血小板,而非损伤它们。NBT和维生素E共同作用可阻断肾上腺素、胶原蛋白和凝血酶引起的聚集,但允许ADP刺激产生一个小的第一波聚集。ADP和凝血酶均可诱导经维生素E-NBT处理的血小板发生形态改变、伪足形成以及有限程度的内部收缩,而肾上腺素和胶原蛋白未能显著改变盘状形态。这种对聚集剂的反应模式与用阿司匹林和吲哚美辛预处理的血小板中观察到的反应相同,阿司匹林和吲哚美辛均为血小板前列腺素合成的强效抑制剂。此外,NBT-维生素E实际上阻断了不受阿司匹林和吲哚美辛影响的第一波聚集。这些发现支持了这样一种观点,即花生四烯酸转化为活化状态是前列腺素合成中的一个重要步骤,并且电子转移或氧化还原反应与血小板黏附性的发展密切相关。