INHIBITION OF PLATELET DEPOSITION BY COMBINED HIRULOG AND ASPIRIN IN A RAT CAROTID ENDARTERECTOMY MODEL

被引:10
作者
HAMELINK, JK
TANG, DB
BARR, CF
JACKSON, MR
REID, TJ
GOMEZ, ER
ALVING, BM
机构
[1] WALTER REED ARMY MED CTR,DEPT HEMATOL & VASC BIOL,WASHINGTON,DC 20307
[2] WALTER REED ARMY MED CTR,DEPT BIOMETR & STAT,WASHINGTON,DC 20307
关键词
D O I
10.1016/S0741-5214(95)70292-X
中图分类号
R61 [外科手术学];
学科分类号
摘要
Purpose: Hirulog, a thrombin-specific inhibitor, has shown efficacy in reducing arterial thrombosis in patients treated with aspirin who require angioplasty or have unstable angina. In this study, the effect of hirulog on reducing deposition of indium(111)-labeled platelets was assessed in a surgical model of aspirin-treated rats undergoing carotid endarterectomy. Methods: Animals were randomly assigned to one of five groups: control (no aspirin or hirulog); aspirin alone (10 mg/kg); aspirin plus low-dose hirulog (0.2 mg/kg bolus followed by 0.5 mg/kg/hr); aspirin plus medium-dose hirulog (0.4 mg/kg bolus followed by 1.0 mg/kg/hr); or aspirin plus high-dose hirulog (0.6 mg/kg bolus followed by 1.5 mg/kg/hr). Hirulog was infused before surgery and continued until termination of the experiment 30 minutes after endarterectomy. Results: Platelet deposition in rats receiving aspirin atone was reduced by 19% +/- 23% SE (p = 0.26) compared with controls. Deposition in aspirin-treated groups receiving low-, medium-, and high-dose hirulog decreased in a dose-dependent manner by 37% +/- 20% (p = 0.048), 44% +/- 19% (p = 0.061), and 56% +/- 13% (p = 0.022), respectively. As the dose of hirulog was increased, the plasma hirulog levels and activated partial thromboplastin time ratios (final:initial) also increased in a dose-dependent manner. The mean plasma hirulog levels ranged from 0.74 +/- 0.08 mu g/ml in the low-dose hirulog group to 2.55 +/- 0.08 mu g/ml in the high-dose hirulog group, and the corresponding activated partial thromboplastin time ratios were 1.5 +/- 0.12 (p = 0.001) and 3.3 +/- 0.63 (p = 0.001). Bleeding was easily controlled by local hemostatic measures for all experimental groups. Conclusion: Hirulog causes significant decrease in In-111-labeled platelet deposition in aspirin-treated rats subjected to microsurgical endarterectomy at doses that allow surgical hemostasis to be easily established.
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页码:492 / 498
页数:7
相关论文
共 32 条
[1]  
ARMITAGE P, 1987, STATISTICAL METHODS, P90
[2]   ANTICOAGULANT EFFECTS OF HIRULOG, A NOVEL THROMBIN INHIBITOR, IN PATIENTS WITH CORONARY-ARTERY DISEASE [J].
CANNON, CP ;
MARAGANORE, JM ;
LOSCALZO, J ;
MCALLISTER, A ;
EDDINGS, K ;
GEORGE, D ;
SELWYN, AP ;
ADELMAN, B ;
FOX, I ;
BRAUNWALD, E ;
GANZ, P .
AMERICAN JOURNAL OF CARDIOLOGY, 1993, 71 (10) :778-782
[3]  
DABAGHI SF, 1992, CIRCULATION, V86, P261
[4]  
FAREED J, 1991, HAEMOSTASIS, V21, P64
[5]  
FOX I, 1993, THROMB HAEMOSTASIS, V69, P157
[6]   ASPIRIN AS A THERAPEUTIC AGENT IN CARDIOVASCULAR-DISEASE [J].
FUSTER, V ;
DYKEN, ML ;
VOKONAS, PS ;
HENNEKENS, C .
CIRCULATION, 1993, 87 (02) :659-675
[7]  
GLANTZ SA, 1990, PRIMER APPLIED REGRE, P272
[8]   IMPROVEMENT IN EARLY SAPHENOUS-VEIN GRAFT PATENCY AFTER CORONARY-ARTERY BYPASS-SURGERY WITH ANTIPLATELET THERAPY - RESULTS OF A VETERANS ADMINISTRATION COOPERATIVE STUDY [J].
GOLDMAN, S ;
COPELAND, J ;
MORITZ, T ;
HENDERSON, W ;
ZADINA, K ;
OVITT, T ;
DOHERTY, J ;
READ, R ;
CHESLER, E ;
SAKO, Y ;
LANCASTER, L ;
EMERY, R ;
SHARMA, GVRK ;
JOSA, M ;
PACOLD, I ;
MONTOYA, A ;
PARIKH, D ;
SETHI, G ;
HOLT, J ;
KIRKLIN, J ;
SHABETAI, R ;
MOORES, W ;
ALDRIDGE, J ;
MASUD, Z ;
DEMOTS, H ;
FLOTEN, S ;
HAAKENSON, C ;
HARKER, LA .
CIRCULATION, 1988, 77 (06) :1324-1332
[9]   RELATIVE EFFICACY OF ANTITHROMBIN COMPARED WITH ANTIPLATELET AGENTS IN ACCELERATING CORONARY THROMBOLYSIS AND PREVENTING EARLY REOCCLUSION [J].
HASKEL, EJ ;
PRAGER, NA ;
SOBEL, BE ;
ABENDSCHEIN, DR .
CIRCULATION, 1991, 83 (03) :1048-1056
[10]   EFFECTS OF THROMBIN INHIBITION ON THE DEVELOPMENT OF ACUTE PLATELET-THROMBUS DEPOSITION DURING ANGIOPLASTY IN PIGS - HEPARIN VERSUS RECOMBINANT HIRUDIN, A SPECIFIC THROMBIN INHIBITOR [J].
HERAS, M ;
CHESEBRO, JH ;
PENNY, WJ ;
BAILEY, KR ;
BADIMON, L ;
FUSTER, V .
CIRCULATION, 1989, 79 (03) :657-665