Relaxation of human temporal artery by endothelin ET(B) receptors

被引:9
作者
Lucas, GA
White, LR
Juul, R
Cappelen, J
Aasly, J
Edvinsson, L
机构
[1] UNIV TRONDHEIM HOSP,DEPT NEUROL,N-7006 TRONDHEIM,NORWAY
[2] UNIV TRONDHEIM HOSP,DEPT NEUROSURG,N-7006 TRONDHEIM,NORWAY
[3] UNIV LUND HOSP,DEPT INTERNAL MED,S-22185 LUND,SWEDEN
关键词
human temporal artery; endothelin; endothelin receptors; endothelin antagonists; FR; 139317; bosentan; IRL; 1620; indomethacin; nitric oxide synthase inhibitor; vasoactive;
D O I
10.1016/S0196-9781(96)00177-5
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
Endothelin receptors have been characterized in human temporal artery by molecular biological methods and in vitro pharmacology. Reverse transcriptase-polymerase chain reaction was used to detect mRNA encoding ET(A) and ET(B) receptors in normal and endothelium-denuded arteries. Vasomotor response experiments with a specific ET(A) antagonist (FR 139317) suggested the presence of ET(A) subtypes. Marked ET(B)-mediated relaxation was obtained with ET-3 when ET(A) activity was blocked in precontracted arteries. Relaxation was significantly reduced by bosentan, indomethacin, and a nitric oxide synthase inhibitor. It may be speculated that the relaxant activity is mediated through ET(B1) receptors. Copyright (C) 1996 Elsevier Science Inc.
引用
收藏
页码:1139 / 1144
页数:6
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