Borowska A, Lauri D, Maggi A, Dejana E, de Gaetano G, Donati M B, Pangrazzi J
Istituto di Ricerche Farmacologiche Mario Negri, Milano, Italy.
Br J Haematol. 1988 Mar;68(3):339-44. doi: 10.1111/j.1365-2141.1988.tb04211.x.
Different low molecular weight (LMW) heparins were tested on primary haemostasis in rats. Four preparations were studied; one was devoid of any effect on the bleeding time, while the other three prolonged the bleeding time to varying extents. As a consequence we studied the effect of these heparins on platelet aggregation. The fractions which prolonged the bleeding time, also inhibited the ex vivo and in vitro platelet aggregation, whereas the one devoid of any effect on the bleeding time did not affect platelet aggregation. Similar results were obtained using both platelet-rich plasma (PRP) and gel-filtered platelets. The in vitro response of platelets to aggregating agents may offer a parameter to detect the presence of 'bleeding factor(s)' in some LMW heparin preparations.
对不同的低分子量(LMW)肝素进行了大鼠原发性止血试验。研究了四种制剂;一种对出血时间没有任何影响,而其他三种则不同程度地延长了出血时间。因此,我们研究了这些肝素对血小板聚集的影响。延长出血时间的组分也抑制了体外和体内血小板聚集,而对出血时间没有任何影响的组分则不影响血小板聚集。使用富血小板血浆(PRP)和凝胶过滤血小板均得到了类似结果。血小板对聚集剂的体外反应可能提供一个参数,用于检测某些低分子量肝素制剂中“出血因子”的存在。