Dendroaspis natriuretic peptide binds to the natriuretic peptide clearance receptor

被引:38
|
作者
Johns, Douglas G. [1 ]
Ao, Zhaohui
Heidrich, Bradley J.
Hunsberger, Gerald E.
Graham, Taylor
Payne, Lisa
Elshourbagy, Nabil
Lu, Quinn
Aiyar, Nambi
Douglas, Stephen A.
机构
[1] GlaxoSmithKline, Vasc Biol & Thrombosis Dept, Cardiovasc & Urogenital Ctr Excellence Drug Disco, King Of Prussia, PA 19406 USA
[2] GlaxoSmithKline, Resp & Inflammatory Dis Ctr Excellence Drug Disco, King Of Prussia, PA 19406 USA
[3] GlaxoSmithKline, Gene Express & Prot Biochem, King Of Prussia, PA 19406 USA
关键词
natriuretic peptides; natriuretic peptide clearance receptor; NPR-C; heart failure; DNP; Dendroaspis natriuretic peptide;
D O I
10.1016/j.bbrc.2007.04.079
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
Dendroaspis natriuretic peptide (DNP) is a newly-described natriuretic peptide which lowers blood pressure via vasodilation. The natriuretic peptide clearance receptor (NPR-C) removes natriuretic peptides from the circulation, but whether DNP interacts with human NPR-C directly is unknown. The purpose of this study was to test the hypothesis that DNP binds to NPR-C. ANP, BNP, CNP, and the NPR-C ligands AP-811 and cANP(4-23) displaced [I-125]-ANP from NPR-C with pM-to-nM K-i values. DNP displaced [I-125]-ANP from NPR-C with nM potency, which represents the first direct demonstration of binding of DNP to human NPR-C. DNP showed high pM affinity for the GGA receptor and no affinity for GC-B (K-i > 1000 nM). DNP was nearly 10-fold more potent than ANP at stimulating cGMP production in GGA expressing cells. Blockade of NPR-C might represent a novel therapeutic approach in augmenting the known beneficial actions of DNP in cardiovascular diseases such as hypertension and heart failure. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:145 / 149
页数:5
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