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体内凝血酶生成后狒狒的凝血和纤溶反应——白细胞介素6的作用

The coagulation and fibrinolytic responses of baboons after in vivo thrombin generation--effect of interleukin 6.

作者信息

Kruithof E K, Mestries J C, Gascon M P, Ythier A

机构信息

Division of Angiology and Hemostasis, University Hospital, Geneva, Switzerland.

出版信息

Thromb Haemost. 1997 May;77(5):905-10.

PMID:9184401
Abstract

Disseminated intravascular coagulation (DIC) may lead to severe thrombotic or hemorrhagic complications. The present work was undertaken to study the effect of interleukin 6 (IL-6) on variations of key coagulation and fibrinolytic parameters in plasma in a baboon model of experimental DIC induced by injection of factor Xa and phospholipids at dosages leading to partial (48%) or complete fibrinogen depletion. Transient increases of D-dimer, fibrinopeptide A, thrombin-antithrombin and the activated partial thromboplastin time were observed. Each parameter had a particular (time and Xa/phospholipid dose dependent) pattern of changes. The principal effect of IL-6 was a more rapid restoration of fibrinogen concentrations and of overall coagulation tests. Injection of factor Xa/phospholipids led also to a rapid increase of tissue-type plasminogen activator (t-PA) the extent of which was dependent on Xa/phospholipid dose. Pretreatment with IL-6 induced a threefold increase of basal t-PA and a corresponding increase of the t-PA response. Plasminogen activator inhibitor type 1 (PAI-1) concentrations did not change after low dose Xa/phospholipids, but increased eightfold after high dose Xa/phospholipids, IL-6 pretreatment induced within 8 h a twentyfold increase of PAI-1 but no further increase was observed after injection of factor Xa/phospholipids. Thus, in vivo thrombin generation leads to dynamic modifications of the coagulation and fibrinolytic systems. The principal effect of IL-6 is a more rapid normalization of overall coagulation tests, due to normalization of fibrinogen, and an increased t-PA release response which is partially counteracted by increased PAI-1 concentrations.

摘要

弥散性血管内凝血(DIC)可能导致严重的血栓形成或出血并发症。本研究旨在探讨白细胞介素6(IL-6)对狒狒实验性DIC模型血浆中关键凝血和纤溶参数变化的影响,该模型通过注射Xa因子和磷脂诱导,剂量导致部分(48%)或完全纤维蛋白原消耗。观察到D-二聚体、纤维蛋白肽A、凝血酶-抗凝血酶复合物和活化部分凝血活酶时间的短暂增加。每个参数都有特定的(时间和Xa/磷脂剂量依赖性)变化模式。IL-6的主要作用是更快速地恢复纤维蛋白原浓度和整体凝血试验。注射Xa因子/磷脂还导致组织型纤溶酶原激活物(t-PA)迅速增加,其程度取决于Xa/磷脂剂量。IL-6预处理使基础t-PA增加了三倍,并相应增加了t-PA反应。低剂量Xa/磷脂后纤溶酶原激活物抑制剂1(PAI-1)浓度不变,但高剂量Xa/磷脂后增加了八倍,IL-6预处理在8小时内使PAI-1增加了二十倍,但注射Xa因子/磷脂后未观察到进一步增加。因此,体内凝血酶生成导致凝血和纤溶系统的动态改变。IL-6的主要作用是由于纤维蛋白原的正常化使整体凝血试验更快恢复正常,以及t-PA释放反应增加,但PAI-1浓度增加部分抵消了这一作用。

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