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甲磺酸萘莫司他对使用硫酸葡聚糖纤维素柱进行低密度脂蛋白分离置换术中缓激肽生成的影响。

Effect of nafamostat mesilate on bradykinin generation during low-density lipoprotein apheresis using a dextran sulfate cellulose column.

作者信息

Kojima S, Harada-Shiba M, Nomura S, Kimura G, Tsushima M, Kuramochi M, Yamamoto A, Omae T

机构信息

Department of Medicine, National Cardiovascular Center Hospital, Osaka, Japan.

出版信息

ASAIO Trans. 1991 Oct-Dec;37(4):644-8.

PMID:1768503
Abstract

The dextran sulfate (DS) cellulose column usually used for low-density lipoprotein (LDL) apheresis, is an activator of the contact phase of intrinsic coagulation pathway. Hageman factor (factor XII), high-molecular-weight kininogen (HMWK) and prekallikrein (PK) form a complex on the surface of this activator, and bradykinin is released from HMWK by the action of kallikrein converted from PK. Heparin, a frequently used anticoagulant, has no effect on this process, whereas a protease inhibitor, nafamostat mesilate (FUT-175) is thought to inhibit the process. Five patients with severe hypercholesterolemia were treated with LDL apheresis using heparin or FUT-175, each on a different day. During treatment with heparin, factor XII, HMWK, and PK were markedly decreased by passing through the DS column. A distinct generation of bradykinin was observed by passing through the DS column, which led to an increase of blood bradykinin levels from 12.5 +/- 5.3(Mean +/- SEM) pg/ml to 127.3 +/- 67.1 pg/ml after 1000 ml plasma treatment. FUT-175 almost completely suppressed this bradykinin generation. Because bradykinin generated during LDL apheresis seems to have some vasodilative effect, FUT-175 might be preferred in cases with unstable hemodynamics, although this presumption remains to be demonstrated.

摘要

通常用于低密度脂蛋白(LDL)去除术的硫酸葡聚糖(DS)纤维素柱,是内源性凝血途径接触相的激活剂。Hageman因子(因子Ⅻ)、高分子量激肽原(HMWK)和前激肽释放酶(PK)在该激活剂表面形成复合物,并且缓激肽通过由PK转化而来的激肽释放酶的作用从HMWK中释放出来。肝素是一种常用的抗凝剂,对这一过程没有影响,而蛋白酶抑制剂甲磺酸萘莫司他(FUT-175)被认为可抑制该过程。5例严重高胆固醇血症患者分别在不同日期接受使用肝素或FUT-175的LDL去除术治疗。在用肝素治疗期间,因子Ⅻ、HMWK和PK通过DS柱后显著降低。通过DS柱观察到明显的缓激肽生成,在1000 ml血浆治疗后,这导致血液缓激肽水平从12.5±5.3(均值±标准误)pg/ml升高至127.3±67.1 pg/ml。FUT-175几乎完全抑制了这种缓激肽生成。由于在LDL去除术期间生成的缓激肽似乎具有一些血管舒张作用,尽管这一推测仍有待证实,但在血流动力学不稳定的情况下,FUT-175可能更受青睐。

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