Vik-Mo H
Thromb Diath Haemorrh. 1975 Jun 30;33(3):519-27.
A method for assay of lipolytic activity in platelet-poor plasma (PPP), platelet-rich plasma (PRP) and washed human platelets is presented. The lipolytic activity in PRP was about twice the activity in PPP. A significant correlation between lipolysis in platelets and platelet number was established. Molar sodium chloride strongly inhibited lipolytic activity in platelets and a washing procedure did not significantly change the lipolysis. The results indicate that a lipoprotein lipase is bound to human platelets and may play a role in metabolism of triglyceride in platelets.
本文介绍了一种用于检测乏血小板血浆(PPP)、富血小板血浆(PRP)和洗涤后的人血小板中脂解活性的方法。PRP中的脂解活性约为PPP中活性的两倍。血小板中的脂解与血小板数量之间建立了显著的相关性。摩尔氯化钠强烈抑制血小板中的脂解活性,而洗涤过程并未显著改变脂解作用。结果表明,脂蛋白脂肪酶与人血小板结合,可能在血小板中甘油三酯的代谢中发挥作用。