Barkagan Z S, Chuprova A V, Pikanov I V
Klin Lab Diagn. 1995 Sep-Oct(5):29-31.
Trials of a method for assessment of thromboplastic activity of monocyte macrophages in 58 healthy full-term babies in the first days of life, when the hemostasis system undergoes essential changes, revealed an appreciable reduction of the basal thromboplastic activity of monocytes and of its level after 4-hour incubation of these cells on days 3-5 after birth, this reduction being paralleled by progressive hypocoagulation (as shown by coagulogram). The degree of reduction of the thromboplastic activity of monocytes was directly proportional to an increase in the level of fibrin-monomer complexes and fibrinogen degradation products in the blood plasma and serum. This indicates a possible decrease of the production of vitamin-K-dependent coagulation factors not only in the liver, but in monocytes as well. On the other hand, the detected shifts indicate that reduction of thromboplastic activity of monocytes in parallel with increased thrombin formation in the blood are biologically justified, for this decrease equilibrates the thrombogenic shifts in the system of neonatal hemostasis.
在出生后最初几天,当止血系统发生重大变化时,对58名健康足月婴儿的单核巨噬细胞促凝血活性评估方法进行的试验显示,出生后第3 - 5天,单核细胞的基础促凝血活性及其在这些细胞孵育4小时后的水平明显降低,这种降低与进行性低凝状态(如凝血图所示)平行。单核细胞促凝血活性的降低程度与血浆和血清中纤维蛋白单体复合物及纤维蛋白原降解产物水平的升高直接相关。这表明不仅肝脏中维生素K依赖的凝血因子生成可能减少,单核细胞中也可能减少。另一方面,检测到的变化表明,单核细胞促凝血活性降低与血液中凝血酶形成增加同时出现具有生物学合理性,因为这种降低平衡了新生儿止血系统中的血栓形成性变化。