RAT ADRENOMEDULLIN INDUCES A SELECTIVE ARTERIAL VASODILATION VIA CGRP(1) RECEPTORS IN THE DOUBLE-PERFUSED MESENTERIC BED OF THE RAT

被引:18
作者
BERTHIAUME, N
CLAING, A
LIPPTON, H
CADIEUX, A
DORLEANSJUSTE, P
机构
[1] UNIV SHERBROOKE,SCH MED,DEPT PHARMACOL,SHERBROOKE,PQ J1H 5N4,CANADA
[2] TULANE UNIV,SCH MED,DEPT SURG PHARMACOL & INTERNAL MED,NEW ORLEANS,LA 70112
关键词
ADRENOMEDULLIN (1-50); ADRENOMEDULLIN (11-50); CGRP(1) RECEPTORS; RAT MESENTERIC BED; VASODILATION;
D O I
10.1139/y95-154
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present work was undertaken to study the effect of rat adrenomedullin (rADM (1-50) and its C-terminal fragment (11-50)) in the endothelium-intact arterial and venous vasculatures of the rat perfused mesenteric bed. rADM (1-50) and the fragment rADM (11-50) (1-1000 pmol) induced a dose-dependent and endothelium-independent vasodilation on the arterial mesenteric vasculature. However, both peptides were inactive on the venous side of this vascular bed. The CGRP(1) receptor antagonist, hCGRP(8-37) (1 mu M), markedly reduced the vasodilation caused by rADM (1-50) in the arterial mesenteric vasculature. Thus, our results show that rADM (1-50) and its C-terminal fragment rADM (11-50) share properties similar to those of hCGRP. The blocking effect of hCGRP(8-37) supports a role for CGRP(1) receptor activation by adrenomedullin in this vascular preparation.
引用
收藏
页码:1080 / 1083
页数:4
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