Trabucchi E, Foschi D, Marazzi M, Abelli P, Andriuoli G, Lami F, Scagnol I, Del Soldato P, De Santis F, Montorsi W
Institute of General Surgery and Surgical Oncology, University of Milan, Italy.
Haemostasis. 1991;21(1):37-44. doi: 10.1159/000216200.
This study was performed to see whether or not protection of the endothelial cells contributes to the antithrombotic effects of heparin. New Zealand albino rabbits were subjected to jugular vein stasis by single caudal ligation for 2 h. Three treatments were given: saline (control group), heparin (0.2 mg/kg) 5 or 45 min before ligature of the vein. Groups of 6-8 animals were killed at 0, 5, 15, 30 and 120 min. The following parameters were determined: (1) involution and damage of the endothelial cells by scanning and transmission electron microscopy; (2) incidence and weight of thrombi in the lumens of the veins after 2 h stasis, and (3) effects of heparin on APTT and anti-Xa activity. In the control group, stasis caused a considerable involution of the endothelial cells in the first 30 min, followed by fibrin deposition and thrombus generation. Heparin strongly reduced the damage to the endothelial cells, with very evident protection of the cell membranes, and prevented thrombus generation: there were significant decreases in both incidence and weight of thrombi. These effects of heparin were evident both shortly after (maximal anticoagulant effect) and long after (no anticoagulant effect) pretreatment. We think that, under the experimental conditions we used, heparin prevented venous thrombosis at least partially by protection of the endothelial cells, through unknown mechanisms.
本研究旨在观察内皮细胞的保护作用是否有助于肝素的抗血栓形成作用。通过单次尾静脉结扎使新西兰白化兔颈静脉淤滞2小时。给予三种处理:生理盐水(对照组)、在静脉结扎前5分钟或45分钟给予肝素(0.2mg/kg)。在0、5、15、30和120分钟处死6-8只动物的组。测定以下参数:(1)通过扫描和透射电子显微镜观察内皮细胞的退化和损伤;(2)2小时淤滞后静脉腔内血栓的发生率和重量,以及(3)肝素对活化部分凝血活酶时间(APTT)和抗Xa活性的影响。在对照组中,淤滞在最初30分钟内导致内皮细胞明显退化,随后是纤维蛋白沉积和血栓形成。肝素强烈减少了对内皮细胞的损伤,对细胞膜有非常明显的保护作用,并防止了血栓形成:血栓的发生率和重量均显著降低。肝素的这些作用在预处理后不久(最大抗凝作用)和很久之后(无抗凝作用)均很明显。我们认为,在我们使用的实验条件下,肝素至少部分地通过保护内皮细胞、通过未知机制预防了静脉血栓形成。