The effect of intravenous administration of WEB 2086 on PAF-induced platelet aggregation in healthy Friesian calves

被引:5
作者
DaSilva, MB
Gustin, P
Herion, F
Raskinet, R
David, JL
Gougnard, T
Plomteux, G
Desmecht, D
Lekeux, P
机构
[1] UNIV LIEGE,FAC VET MED,LAB PHARMACOL & TOXICOL,B-4000 LIEGE,BELGIUM
[2] UNIV LIEGE,CHU,THROMBOSIS HEMOSTASIS UNIT,B-4000 LIEGE,BELGIUM
[3] UNIV LIEGE,CHU,LAB CLIN TOXICOL,B-4000 LIEGE,BELGIUM
关键词
aggregation; cattle; chromatography; platelet; platelet-activating factor; platelet-rich plasma; thienotriazolodiazepine;
D O I
10.1023/A:1005950622207
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The in vivo ability of the specific PAF-antagonist WEB 2086, a thienotriazolodiazepine, to inhibit platelet-activating factor (PAF) in cattle was investigated by in vitro determination of platelet aggregation curves. WEB 2086 was infused intravenously into a group of 5 healthy male Friesian calves in a dose of 3 mg/kg over 1 min. The resultant inhibition peaked between 30 min and 1 h after administration of WEB 2086. The inhibition was significantly reduced after 3 h and became non-0significant after 6 h, but maximal pre-treatment aggregation had not been restored by 24 h after the injection of WEB 2086. These results confirm previous results obtained in vitro and suggest that WEB 2086 is a potent antagonist of PAF activity in calves. They also suggest that further clinical studies with WEB 2086 in cattle are desirable.
引用
收藏
页码:521 / 531
页数:11
相关论文
共 34 条
[1]   EFFECT OF INTRAVENOUS OR INHALATIVE WEB-2086 ON EXVIVO PLATELET ACTIVATING FACTOR INDUCED PLATELET-AGGREGATION IN MAN [J].
ADAMUS, WS ;
HEUER, H ;
MEADE, CJ ;
KEMPE, ER ;
BRECHT, HM .
PROSTAGLANDINS, 1988, 35 (05) :797-797
[2]  
ADAMUS WS, 1988, EUR J CLIN PHARMACOL, V35, P237
[3]   SAFETY, TOLERABILITY, AND PHARMACOLOGIC ACTIVITY OF MULTIPLE DOSES OF THE NEW PLATELET ACTIVATING FACTOR ANTAGONIST WEB-2086 IN HUMAN-SUBJECTS [J].
ADAMUS, WS ;
HEUER, H ;
MEADE, CJ ;
BRECHT, HM .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1989, 45 (03) :270-276
[4]  
BARNES PJ, 1991, ANN NY ACAD SCI, V629, P193
[5]  
BENVENISTE J, 1979, CR ACAD SCI D NAT, V289, P1037
[6]  
BLANK ML, 1979, BIOCHEM BIOPH RES CO, V90, P523
[7]  
BORN GVR, 1963, J PHYSIOL-LONDON, V168, P178, DOI 10.1113/jphysiol.1963.sp007185
[8]  
BOWERS LD, 1989, CLIN CHEM, P94
[9]  
BRAMBILLA A, 1987, PHARMACOL RES, V19, P147
[10]  
BRAQUET P, 1987, PHARMACOL REV, V39, P97