Shah G A, Nair C H, Dhall D P
Vascular Laboratory, Woden Valley Hospital, ACT, Australia.
Thromb Res. 1987 Feb 1;45(3):257-64. doi: 10.1016/0049-3848(87)90193-9.
Mass-Length ratio of fibrin fibres (microT and microP) derived independently from turbidity and permeability respectively, in networks made in fibrinogen solution and plasma, have been compared under similar conditions of clotting. Amount of fibrinogen conversion to fibrin was similar in both systems when high thrombin concentrations were used. But networks in plasma had significantly thicker fibres (higher microT and microP) than those in fibrinogen solution. This difference arises from differing kinetics of fibrin assembly in the two systems. When lower thrombin concentration is used, fibrin fibre thickness (as indicated by microP and microT) is increased in fibrinogen solution but the fibrin content of the network remains unaltered. In plasma, on the other hand, the fibrin content of the network is decreased, microT remains relatively unchanged while microP increases. The thrombin concentration dependence of the fibrin content of the network in plasma and the bimodal distribution of fibrin fibre thickness explain the breakdown in correlation between microP and microT.
分别从浊度和渗透率独立得出的纤维蛋白纤维的质量-长度比(microT和microP),在纤维蛋白原溶液和血浆中形成的网络中,已在相似的凝血条件下进行了比较。当使用高凝血酶浓度时,两个系统中纤维蛋白原转化为纤维蛋白的量相似。但血浆中的网络纤维明显更粗(更高的microT和microP),比纤维蛋白原溶液中的网络纤维粗。这种差异源于两个系统中纤维蛋白组装的不同动力学。当使用较低的凝血酶浓度时,纤维蛋白原溶液中纤维蛋白纤维的厚度(由microP和microT表示)增加,但网络中的纤维蛋白含量保持不变。另一方面,在血浆中,网络中的纤维蛋白含量降低,microT相对不变,而microP增加。血浆中网络纤维蛋白含量对凝血酶浓度的依赖性以及纤维蛋白纤维厚度的双峰分布解释了microP和microT之间相关性的破坏。