Rosenblum W I, Nelson G H, Cockrell C S, Ellis E F
Thromb Res. 1983 May 15;30(4):347-55. doi: 10.1016/0049-3848(83)90226-8.
Mouse platelets were aggregated by arachidonate, thrombin, collagen and ADP. In general they were, like rat platelets, more aggregative in heparinized PRP than in citrated (3.8%) PRP. Mouse platelets underwent the release reaction when aggregated by arachidonate, collagen and thrombin, but not when stimulated by ADP. The aggregation of the platelets to arachidonate was inhibited by cyclooxygenase inhibitors and by prostacyclin. Studies with tritiated arachidonate showed that mouse platelets possess the lipoxygenase and cyclooxygenase pathways found in other mammalian platelets and produce thromboxane and 12-HETE. The mouse provides a convenient model for the study of many conditions known to affect platelet aggregation. The similarity of mouse platelets to the platelets of other mammals together with the ability to study large numbers of animals at low cost, should encourage further use of mouse platelets.
小鼠血小板可被花生四烯酸、凝血酶、胶原蛋白和二磷酸腺苷(ADP)凝集。一般来说,与大鼠血小板一样,它们在肝素化富血小板血浆(PRP)中比在枸橼酸化(3.8%)PRP中更易凝集。小鼠血小板在被花生四烯酸、胶原蛋白和凝血酶凝集时会发生释放反应,但在被ADP刺激时则不会。血小板对花生四烯酸的凝集作用受到环氧合酶抑制剂和前列环素的抑制。用氚标记的花生四烯酸进行的研究表明,小鼠血小板具有在其他哺乳动物血小板中发现的脂氧合酶和环氧合酶途径,并产生血栓素和12-羟基二十碳四烯酸(12-HETE)。小鼠为研究许多已知影响血小板凝集的情况提供了一个便利的模型。小鼠血小板与其他哺乳动物血小板的相似性,以及以低成本研究大量动物的能力,应会促使人们进一步使用小鼠血小板。