Björk P, Axelsson L, Bergenfeldt M, Ohlsson K
Department of Surgical Pathophysiology, University of Lund, Malmö General Hospital, Sweden.
Scand J Clin Lab Invest. 1988 Apr;48(2):205-11. doi: 10.3109/00365518809085414.
Cleavage of C3, fibronectin, antithrombin III and alpha 2-antiplasmin in human plasma following the addition of increasing amounts of human leucocyte elastase was studied using an in vitro model. The cleavage was correlated with the degree of saturation of the plasma protease inhibitors alpha 2-macroglobulin and alpha 1-protease inhibitor and also with varying amounts of secretory leucocyte protease inhibitor. When alpha 1-protease inhibitor approached saturation, there was a prompt cleavage of all the four plasma proteins studied. The secretory leucocyte protease inhibitor was needed in a concentration of 6 mumol/l in the present model to block this consumption completely. This concentration also gave some protection of alpha 1-protease inhibitor and alpha 2-macroglobulin.
使用体外模型研究了在人血浆中添加越来越多的人白细胞弹性蛋白酶后,C3、纤连蛋白、抗凝血酶III和α2 -抗纤溶酶的裂解情况。这种裂解与血浆蛋白酶抑制剂α2 -巨球蛋白和α1 -蛋白酶抑制剂的饱和程度以及不同量的分泌型白细胞蛋白酶抑制剂相关。当α1 -蛋白酶抑制剂接近饱和时,所研究的所有四种血浆蛋白都会迅速裂解。在本模型中,需要6 μmol/L的分泌型白细胞蛋白酶抑制剂浓度才能完全阻断这种消耗。该浓度也对α1 -蛋白酶抑制剂和α2 -巨球蛋白有一定的保护作用。