α -凝血酶和γ -凝血酶对麻醉绵羊肺液平衡的影响。

R R Garcia-Szabo, D F Kern, R Bizios, J W Fenton, F L Minnear, S K Lo, A B Malik
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引用次数: 12

摘要

我们研究了不同剂量的凝血酶对氟烷麻醉绵羊肺淋巴瘘管肺液平衡的影响。静脉输注亚致死剂量的α -凝血酶(2.5凝血单位/微克),即天然酶,以0.6或1.1 nmol的酶/kg体重量增加平均肺动脉压(Ppa)和肺血管阻力(PVR)两到三倍。这两个参数都以剂量依赖的方式增加。两种剂量下血小板计数均下降50%。低剂量组和高剂量组白细胞计数分别比基线下降35%和75%,两组在输注后60分钟达到比基线低50%的水平。血浆纤维蛋白原浓度在肺淋巴流(Qlym)和淋巴蛋白清除率(Clym)的剂量依赖性增加之前以剂量依赖性的方式下降。肺血管纤维蛋白沉积在注射后30分钟大于180分钟。相比之下,静脉输注缺乏纤维蛋白原识别位点的γ -凝血酶(0.002凝血单位/微克)15分钟,以1.2 nmol酶/kg的剂量,PVR、Ppa、Qlym或Clym没有显著增加。纤维蛋白原浓度没有明显变化,而血小板和白细胞计数在15分钟内下降了25%。肺血管中的纤维蛋白微血栓不太明显。与血管内凝血相关的纤维蛋白沉积可能是介导凝血酶诱导的肺经血管液体和蛋白质交换增加的重要因素。
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Comparison of alpha- and gamma-thrombin on lung fluid balance in anesthetized sheep.

We examined the effects of varying dosages of thrombin on lung fluid balance in halothane-anesthetized sheep prepared with lung lymph fistulas. A 15-min iv infusion of sublethal doses of alpha-thrombin (2.5 clotting units/micrograms), the native enzyme, at 0.6 or 1.1 nmol active enzyme/kg body wt increased the mean pulmonary arterial pressure (Ppa) and pulmonary vascular resistance (PVR) two- to threefold. Neither parameter increased in a dose-dependent manner. Platelet counts decreased 50% with both dosages. Leukocyte counts decreased 35 and 75% from base line in the low- and high-dosage groups, respectively, and reached comparable levels of 50% below base line at 60-min postinfusion in both groups. Plasma fibrinogen concentrations decreased in a dose-dependent manner preceding dose-dependent increases in pulmonary lymph flow (Qlym) and lymph protein clearance (Clym). Fibrin deposition in pulmonary vessels was greater at 30 than at 180 min postinfusion. In contrast, a 15-min iv infusion of gamma-thrombin (0.002 clotting units/micrograms), which lacks the fibrinogen recognition site, at 1.2 nmol active enzyme/kg produced no significant increases in PVR, Ppa, Qlym, or Clym. The fibrinogen concentration did not change significantly, whereas platelet and leukocyte counts decreased 25% within 15 min. Fibrin microthrombi were less prominent in pulmonary vessels. Fibrin deposition associated with intravascular coagulation may be an important factor mediating thrombin-induced increases in pulmonary transvascular fluid and protein exchange.

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