Morizumi Sei, Hiramatsu Yuji, Matsuzaki Kanji, Goto Yukinobu, Sato Shoko, Abe Masakazu, Kato Hideyuki, Matsubara Muneaki, Sakakibara Yuzuru
Department of Cardiovascular Surgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
J Card Surg. 2014 Jan;29(1):35-40. doi: 10.1111/jocs.12254. Epub 2013 Nov 25.
We tested the hypothesis that heparin administration prior to the emergence of tissue factor (TF) would increase plasma TF pathway inhibitor (TFPI) and attenuate TF-mediated thrombin generation during simulated cardiopulmonary bypass (CPB).
Human blood was recirculated for 120 minutes using an oxygenator and roller pump. Four groups were examined: control group (heparin 3.75 U/mL, in donor blood, n = 7), rTF group (heparin + recombinant TF 1000 pg/mL, in donor blood, n = 7), TFPI boost group (heparin, in preheparinized donor blood, n = 8), and rTF + TFPI boost group (heparin + rTF, in preheparinized blood, n = 7). In the two TFPI boost groups, 50 U/kg of heparin was given to the donors intravenously five minutes before donation to boost plasma TFPI levels. Total plasma TFPI, thrombin-antithrombin complex, and prothrombin fragment F1+2 levels were measured before and during CPB.
Preheparinization increased total plasma TFPI levels by a factor of 8.0. Administration of rTF significantly enhanced the generation of F1+2 (p = 0.0002). The heparin-induced TFPI elevation reduced both thrombin-antithrombin complex and F1+2 to control levels in rTF + TFPI boost group (p = 0.0158 for thrombin-antithrombin complex, p < 0.0001 for F1+2 ). F1+2 levels were at all times lower than control levels in TFPI boost group (p < 0.0001).
Heparin-induced TFPI elevation attenuates TF-mediated thrombin generation. Early heparin administration prior to the emergence of plasma TF may represent a novel strategy for controlling thrombin generation by the extrinsic coagulation pathway during CPB.
我们检验了这样一个假设,即在组织因子(TF)出现之前给予肝素会增加血浆TF途径抑制剂(TFPI),并在模拟体外循环(CPB)期间减弱TF介导的凝血酶生成。
使用氧合器和滚压泵将人体血液再循环120分钟。检查了四组:对照组(供体血液中肝素浓度为3.75 U/mL,n = 7),rTF组(供体血液中肝素+重组TF 1000 pg/mL,n = 7),TFPI增强组(预肝素化供体血液中的肝素,n = 8),以及rTF + TFPI增强组(预肝素化血液中肝素+rTF,n = 7)。在两个TFPI增强组中,在献血前5分钟给供体静脉注射50 U/kg肝素以提高血浆TFPI水平。在CPB之前和期间测量血浆总TFPI、凝血酶 - 抗凝血酶复合物和凝血酶原片段F1 + 2水平。
预肝素化使血浆总TFPI水平提高了8.0倍。给予rTF显著增强了F1 + 2的生成(p = 0.0002)。肝素诱导的TFPI升高使rTF + TFPI增强组中的凝血酶 - 抗凝血酶复合物和F1 + 2均降至对照水平(凝血酶 - 抗凝血酶复合物p = 0.0158,F1 + 2 p < 0.0001)。TFPI增强组中的F1 + 2水平在所有时间均低于对照水平(p < 0.0001)。
肝素诱导的TFPI升高减弱了TF介导的凝血酶生成。在血浆TF出现之前早期给予肝素可能代表一种在CPB期间通过外源性凝血途径控制凝血酶生成的新策略。