首都医科大学学报 ›› 2008, Vol. 29 ›› Issue (3): 311-314.

• 基础研究 • 上一篇    下一篇

兔激素性股骨头坏死凝血-纤溶系统的变化

王泳1, 高春锦2, 庞宝森3, 杨晋才4, 李海东1, 武连华2   

  1. 1. 首都医科大学附属复兴医院高压氧科;2. 首都医科大学附属北京朝阳医院高压氧科;3. 首都医科大学附属北京朝阳医院呼吸科;4. 首都医科大学附属北京朝阳医院骨科
  • 收稿日期:2007-11-23 修回日期:1900-01-01 出版日期:2008-06-24 发布日期:2008-06-24
  • 通讯作者: 杨晋才

The Changes in Coagulation-fibrinolysis Systems in Rabbits with Steroid-induced Avascular Necrosis of the Femoral Head

Wang Yong1, Gao Chunjin2, Pang Baosen3, Yang Jincai4, Li Haidong1, Wu Lianhua2   

  1. 1. Department of Hyperbaric Oxygen, Fuxing Hospital, Capital Medical University;2. Department of Hyperbaric Oxygen, Beijing Chaoyang Hospital, Capital Medical University;3. Department of Respiratory Diseases, Beijing Chaoyang Hospital, Capital Medical University;4. Department of Orthopaedics, Beijing Chaoyang Hospital, Capital Medical University
  • Received:2007-11-23 Revised:1900-01-01 Online:2008-06-24 Published:2008-06-24

摘要: 目的 观察兔激素性股骨头坏死凝血-纤溶系统指标的变化,探讨激素性股骨头坏死的发病机制.方法 建立激素性股骨头坏死的动物模型,各组分别采血测定血浆抗凝血酶Ⅲ(AT-Ⅲ)、血栓调节蛋白(TM)、组织型纤溶酶原激活物(tPA)、纤溶酶原激活物抑制剂-1(PAI-1)的含量.结果 1)凝血系统指标变化:AT-Ⅲ:给药24h后明显升高(P<0.05),然后开始下降,1周时下降最明显(P<0.05);TM:给药后24h开始升高(P<0.01),1周时升高最明显(P<0.01).2)纤溶系统指标变化:tPA:给药后24h至2周时均明显降低(P<0.01);PAI-1:给药后24h至2周时均明显升高(P<0.01).结论 模型动物的凝血-纤溶系统存在明显功能障碍,这可能是激素性股骨头坏死的发病机制之一.

关键词: 激素, 股骨头坏死, 凝血, 纤溶

Abstract: Objective To observe the changes in parameters of coagulation-fibrinolysis systems in rabbits with steroid-induced avascular osteonecrosis of femoral head(SANFH) and to investigate the pathogenesis of SANFH.Methods Experimental animal and grouping:Male adult New Zealand white rabbits,ranging in weight from 2.5 to 3.5 kg,were obtained from experimental center of Capital Medical University and randomly divided into seven groups including Group N(normal group);Groups M24 h,M48 h,M1,M2,M4,M6(model groups).Eight rabbits for each group.Animal models of steroid-induced avascular osteonecrosis of the femoral head were established according to Yamamoto T et al's method.Animals in model group received lipopolysaccharide(LPS) 20 μg/kg intravenously 2 times at an interval of 24 hours,methylprednisolone 20 mg/kg injected were intramuscularly into the gluteus medius 3 times at intervals of 24 hours after the second injection of LPS.The plasma levels of antithrombin-Ⅲ(AT-Ⅲ),thrombomodulin(TM),tissue-type plasminogen activator(tPA) and plasminogen activator inhibitor-1(PAI-1) were measured in each group.Results 1) Coagulation system:AT-Ⅲ:Compare with the normal group,the plasma levels of AT-Ⅲ in the model group were significantly higher at 24 hours after the first injection of LPS(P<0.05),then began to decrease at 48 hours,most obviously at 1 week(P<0.05);TM:Compare with the normal group,the plasma levels of TM in the model group began to increase at 24 hours after the first injection of LPS(P<0.01),most obviously at 1 week(P<0.01).2) Fibrinolysis system:tPA:The plasma levels of tPA in the model group were significantly lower than those in the normal group from 24 hours to 2 weeks after the first injection of LPS(P<0.01);PAI-1:The plasma levels of PAI-1 in the model group were significantly higher than those in the model group from 24 hours to 2 weeks after the first injection of LPS(P<0.01).Conclusion Marked dysfunction of coagulation-fibrinolysis systems has been found in the model animals,which may be one of the pathogeneses of SANFH.

Key words: steroid, avascular necrosis of the femoral head, coagulation, fibrinolysis

中图分类号: