Endothelial action of thienopyridines and thienopyrimidinones isolated guinea in the pig heart

被引:52
作者
Jakubowski, A [1 ]
Chlopicki, S [1 ]
Olszanecki, R [1 ]
Jawien, J [1 ]
Lomnicka, M [1 ]
Dupin, JP [1 ]
Gryglewski, RJ [1 ]
机构
[1] Jagiellonian Univ, Sch Med, Dept Expt Pharmacol, Chair Pharmacol, PL-31531 Krakow, Poland
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2005年 / 72卷 / 02期
关键词
D O I
10.1016/j.plefa.2004.10.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antiplatelet thienopyridines (ticlopidine, clopidogrel) and their thienopyrimidinone congeners. induce prostacyclin-dependent thrombolysis in vivo. Here we tested whether thienopyridines (ticlopidine, clopidogrel. and its enantiomer without antiplatelet properties) and structurally related thienopyrimidinones release NO from coronary endothelium in the isolated guinea pig heart, perfused according to Langendorff technique. The involvement of endothelium-derived NO in coronary vasodilation induced by these agents was assessed by effect of L-N-G-nitro-arginine methyl ester (L-NAME). In addition. effect of thienopyridines or thienopyrimidinones on nitrite accumulation in cultured endothelium was assayed. Tienopyridines (10-100 mumoI L-1) and thienopyrimidinones (10-30 mumol L-1) produced concentration-dependent increase in coronary flow comparable to that induced by acetylcholine (0.1 mumol L-1) or bradykinin (3 nmol L-1) which was inhibited by L-NAME (by 50-70%) but not by indomethacin. Furthermore, thienopyridines and thienopyrimidinones caused NO release from cultured endothelial cells. In conclusion, both thienopyridines independently from their antiplatelet action and their thienopyrimidinone congeners that are devoid of antiplatelet action stimulate coronary endothelium to release NO. Endothelial action of these compounds merits further investigation. (C) 2004 Elsevier Ltd. All rights reserved.
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页码:139 / 145
页数:7
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