[H-3] DUP-753, A HIGHLY POTENT AND SPECIFIC RADIOLIGAND FOR THE ANGIOTENSIN-II-1 RECEPTOR SUBTYPE

被引:94
作者
CHIU, AT
MCCALL, DE
ALDRICH, PE
TIMMERMANS, PBMWM
机构
[1] Medical Products Department E.I. du Pont de Nemours and Company, Wilmington, DE 19880-0400
关键词
D O I
10.1016/0006-291X(90)91575-D
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
[3H]DuP 753, a nonpeptide angiotensin II (AII) receptor antagonist radioligand, was used to characterize a subtype of AII receptors in rat adrenal cortical microsomes. By Scatchard analysis, a single class of DuP 753 binding sites was found with an affinity of 6.4 nM and a Bmax of 1.3 pmol/mg protein. These sites were saturable and readily reversible. Angiotensin (I, II, III) expressed the same affinities and order of potency for these binding sites as those labeled by [3H]AII for the AII-1 sites. The affinities expressed by nonpeptide AII antagonists were commensurate with their inhibitory potencies on AII-1 receptors. PD123177, an AII-2 specific ligand, and other non-AII peptides showed no inhibitory action. These data together with the differential tissue distribution strongly support our conclusion that [3H]DuP 753 is a potent and highly specific radioligand for the AII-1 receptors. © 1990.
引用
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页码:1195 / 1202
页数:8
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