ENDOTHELIUM-DEPENDENT RELAXATION TO SUBSTANCE-P IN HUMAN UMBILICAL ARTERY IS MEDIATED VIA PROSTANOID SYNTHESIS

被引:20
作者
BODELSSON, G [1 ]
STJERNQUIST, M [1 ]
机构
[1] LUND UNIV,MALMO GEN HOSP,DEPT OBSTET & GYNAECOL MALMO,S-21401 MALMO,SWEDEN
关键词
ENDOTHELIUM; HUMAN UMBILICAL ARTERY; INDOMETHACIN; RELAXATION; SUBSTANCE P;
D O I
10.1093/oxfordjournals.humrep.a138580
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
To investigate the relaxatory effect and mode of action of substance P in the human umbilical artery, ring segments of the artery were suspended in organ baths to record the circular motor activity. Substance P induced a significant relaxation in segments with intact endothelium pre-contracted by potassium or 5-hydroxytryptamine. Segments devoid of their endothelium failed to relax when challenged with substance P. The relaxation induced by substance P was inhibited by the cyclo-oxygenase antagonist indomethacin, while the nitric oxide-synthetase inhibitor L-N-G-monomethylarginine was without effect. These findings suggest that the relaxatory effect of substance P in the human umbilical artery is dependent on an intact endothelium. In contrast to the case in most other vessels, the relaxation is not mediated via the release of endothelium-derived relaxing factor, but seems to be dependent on prostanoid synthesis.
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页码:733 / 737
页数:5
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