Giles A R, Mann K G, Nesheim M E
Department of Pathology, Queen's University at Kingston, Ontario, Canada.
Br J Haematol. 1988 Aug;69(4):491-7. doi: 10.1111/j.1365-2141.1988.tb02405.x.
A combination of phosphatidylcholine-phosphatidylserine lipid vesicles (PCPS), as a source of coagulant active phospholipid, when infused with factor Xa bypasses factor VIII in vivo. To demonstrate this, a reproducible model of bleeding in haemophilic dogs was used. Control studies were performed in normal dogs. In initial studies, factor Xa/PCPS at a dose of 6.5 x 10(-12) and 4.0 x 10(-7) moles/kg respectively failed to correct the abnormal bleeding in the haemophilic animals and initiated a bleeding diathesis in the normal controls. Coagulation studies and immunoblotting demonstrated activation of protein C and an anticoagulant effect resulting from significant falls in the levels of factors V and VIII. Adjustment of the dose of factor Xa/PCPS to 2.6 x 10(-11) and 4.0 x 10(-8) moles/kg respectively produced an immediate haemostatic effect in both haemophilic and normal animals with bleeding stopping within 15-30 s. Despite this observation, protein C activation was again noted. It is concluded that the presence of coagulant active phospholipid and factor Xa in prothrombin complex concentrates may explain the observed factor VIII bypassing activity of these preparations and that the use of a controlled formulation of these two components may provide a more effective approach to the management of patients with factor VIII inhibitors.
作为促凝血活性磷脂来源的磷脂酰胆碱 - 磷脂酰丝氨酸脂质囊泡(PCPS)与凝血因子Xa联合注入体内时可绕过凝血因子VIII。为证明这一点,使用了血友病犬的可重复出血模型。在正常犬中进行了对照研究。在初步研究中,凝血因子Xa/PCPS剂量分别为6.5×10⁻¹²和4.0×10⁻⁷摩尔/千克时,未能纠正血友病动物的异常出血,反而在正常对照中引发了出血素质。凝血研究和免疫印迹显示蛋白C激活以及因因子V和VIII水平显著下降导致的抗凝作用。将凝血因子Xa/PCPS剂量分别调整为2.6×10⁻¹¹和4.0×10⁻⁸摩尔/千克后,在血友病和正常出血动物中均产生了立即止血效果,出血在15 - 30秒内停止。尽管有此观察结果,但再次注意到蛋白C激活。结论是,凝血酶原复合物浓缩物中促凝血活性磷脂和凝血因子Xa的存在可能解释了这些制剂中观察到的因子VIII旁路活性,并且使用这两种成分的受控制剂可能为治疗因子VIII抑制剂患者提供更有效的方法。