CHARACTERIZATION OF ENDOTHELIN RECEPTORS AND LOCALIZATION OF I-125 ENDOTHELIN-1 BINDING-SITES IN HUMAN UMBILICAL ARTERY

被引:27
作者
BODELSSON, G [1 ]
STJERNQUIST, M [1 ]
机构
[1] LUND UNIV,GEN HOSP,DEPT OBSTET & GYNECOL,S-21401 MALMO,SWEDEN
关键词
AUTORADIOGRAPHY; CA2+ CHANNEL; ENDOTHELIN; ENDOTHELIUM; UMBILICAL ARTERY (HUMAN); ENDOTHELIN RECEPTOR;
D O I
10.1016/0014-2999(93)90526-N
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The mechanisms of endothelin-1-induced contractile response in the human umbilical artery were investigated in vitro. Autoradiography revealed I-125-endothelin-1 binding sites in the smooth muscle layer of the vessel wail. Endothelin-1 and sarafotoxin S6b induced concentration-dependent contractions while endothelin-3 was virtually without contractile effect. The endothelin ET(A) receptor antagonist BQ 123 did not affect the contraction to endothelin-1 but antagonized the contraction to sarafotoxin S6b. The contraction to endothelin-1 and sarafotoxin S6b was diminished by both verapamil and nicardipine. It can be concluded that endothelin-1 is a vasoconstrictor in the human umbilical artery, probably acting via more than one contraction-mediating receptor. The I-125-endothelin-1 binding sites demonstrated in the smooth muscle layer of the vessel may correspond to receptors mediating the contractile effect. The mechanisms of action seems to involve activation of Ca2+ channels. The present study does not give any evidence for interaction of endothelin-1 with other endothelium-derived vasoactive agents in this vessel.
引用
收藏
页码:299 / 305
页数:7
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