THE ENDOTHELIN RECEPTOR ANTAGONIST, BQ-123, INHIBITS ANGIOTENSIN II-INDUCED CONTRACTIONS IN RABBIT AORTA

被引:61
作者
WEBB, ML
DICKINSON, KEJ
DELANEY, CL
LIU, ECK
SERAFINO, R
COHEN, RB
MONSHIZADEGAN, H
MORELAND, S
机构
[1] BRISTOL MYERS SQUIBB,PHARMACEUT RES INST,DEPT PHARMACOL,POB 4000,PRINCETON,NJ 08543
[2] BRISTOL MYERS SQUIBB,PHARMACEUT RES INST,DEPT CARDIOVASC BIOCHEM,PRINCETON,NJ 08543
关键词
D O I
10.1016/0006-291X(92)91710-8
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
The purpose of this study was to examine the specificity of the cyclic pentapeptide ETA receptor antagonist BQ-123. BQ-123 competitively antagonized endothelin-1-induced contractions in rabbit aorta, increases in inositol phosphates in cultured rat vascular smooth muscle A10 cells, and binding of [125I]endothelin-1 to the cloned ETA receptor cDNA expressed in Cos 7 cells. In contrast, BQ-123 was a weak antagonist of [125I]endothelin-3 binding to rat cerebellar membranes and to membranes from Cos 7 cells transfected with the cloned ETB receptor cDNA. BQ-123 shifted concentration-response curves in isolated rabbit aorta elicited by angiotensin II, but did not bind to angiotensin II receptors nor affect angiotensin II-induced increases in inositol phosphates. BQ-123 also did not affect contractions induced by KCl or norepinephrine. These data suggest that endothelin may play a role in angiotensin II-induced contractions of rabbit aorta. © 1992.
引用
收藏
页码:887 / 892
页数:6
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