Heparin coating of tantalum coronary stents reduces surface thrombin generation but not factor IXa generation

被引:36
作者
Blezer, R
Cahalan, L
Cahalan, PT
Lindhout, T
机构
[1] Maastricht Univ, Dept Biochem, Cardiovasc Res Inst, NL-6200 MD Maastricht, Netherlands
[2] Medtron Bakken Res Ctr, Dept Biomat Technol, Maastricht, Netherlands
关键词
stent; blood coagulation; flow; immobilized heparin;
D O I
10.1097/00001721-199807000-00006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the present study we used an in-vitro technique to examine initiation and propagation of blood coagulation at the surface of tantalum coronary stents exposed to flowing platelet-rich and platelet-free plasma. The time course of factor IXa production at the surface of the stent was not influenced by platelets. In spite of a significant factor IXa production, no thrombin activity was detected when the tantalum stent was exposed to platelet-free plasma; only when the stent was exposed to platelet-rich plasma was extensive thrombin production observed. These findings indicate that tantalum triggers blood coagulation, but that (adherent) platelets are essential for thrombin generation. Heparin-coated tantalum stents exposed to flowing platelet-rich plasma showed that factor IXa generation was slightly reduced compared with the bare stent. However, the heparin coating drastically delayed the onset of thrombin generation and largely reduced the steady-state production of thrombin. We found a clear relationship between the antithrombin binding capacity and the antithrombogenic potential of the heparin-coated stents. The mode of action of immobilized heparin is thought to abrogate thrombin generation by inhibiting thrombin-dependent positive feedback reactions at the surface of the coronary stent. (C) 1998 Lippincott-Raven Publishers.
引用
收藏
页码:435 / 440
页数:6
相关论文
共 25 条
[1]   Initiation and propagation of blood coagulation at artificial surfaces studied in a capillary flow reactor [J].
Blezer, R ;
Willems, GM ;
Cahalan, PT ;
Lindhout, T .
THROMBOSIS AND HAEMOSTASIS, 1998, 79 (02) :296-301
[2]  
Blezer R, 1997, J BIOMED MATER RES, V37, P108, DOI 10.1002/(SICI)1097-4636(199710)37:1<108::AID-JBM13>3.0.CO
[3]  
2-C
[4]  
DeScheerder I, 1997, CIRCULATION, V95, P1549
[5]   Stents for intracoronary placement: Current status and future directions [J].
Eeckhout, E ;
Kappenberger, L ;
Goy, JJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1996, 27 (04) :757-765
[6]  
ELGUE G, 1993, THROMB HAEMOSTASIS, V70, P289
[7]   The current status of stenting - Pathobiology [J].
Fleser, A ;
Leclere, G .
TRENDS IN CARDIOVASCULAR MEDICINE, 1997, 7 (01) :24-28
[8]   Reduction in thrombotic events with heparin-coated Palmaz-Schatz stents in normal porcine coronary arteries [J].
Hardhammar, PA ;
vanBeusekom, HMM ;
Emanuelsson, HU ;
Hofma, SH ;
Albertsson, PA ;
Verdouw, PD ;
Boersma, E ;
Serruys, PW ;
vanderGiessen, WJ .
CIRCULATION, 1996, 93 (03) :423-430
[9]  
HENDRIX H, 1983, J BIOL CHEM, V258, P3637
[10]   ANTITHROMBIN ACTIVITY OF SURFACE-BOUND HEPARIN STUDIED UNDER FLOW CONDITIONS [J].
LINDHOUT, T ;
BLEZER, R ;
SCHOEN, P ;
WILLEMS, GM ;
FOUACHE, B ;
VERHOEVEN, M ;
HENDRIKS, M ;
CAHALAN, L ;
CAHALAN, PT .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (10) :1255-1266