Functional properties of PFR(Tic)amide and BIBP3226 at human neuropeptide FF2 receptors

被引:19
作者
Engström, M
Wurster, S
Savola, JM
Panula, P
机构
[1] Juvantia Pharma Ltd, Pharm, FIN-20520 Turku, Finland
[2] Abo Akad Univ, Inst Biol, Dept Biol, FIN-20520 Turku, Finland
关键词
neuropeptide FF; antagonist; PFR(Tic)amide; BIBP3226; neuropeptides; S-35]GTP gamma S binding assay; NPFF2; receptor; super-agonist;
D O I
10.1016/j.peptides.2003.10.009
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 functional characteristics of two putative neuropeptide FF (NPFF) antagonists, BIBP3226 and PFR(Tic)amide, on the human neuropeptide FF receptor subtype 2 (hNPFF2) were investigated. Surprisingly, PFR(Tic)amide was shown to exhibit agonist properties in the [S-35]guanosine-5'-O-(3-thio)triphosphate ([S-35]GTPgammaS) binding assay. The efficacy of PFR(Tic)amide was significantly greater than that of (1DMe)Y8Fa, a stable analog of NPFF, and PFR(Tic)amide can therefore be classified as a 'super-agonist'. BIBP3226 did act as a reversible competitive antagonist on the hNPFF2 receptor. However, high concentrations of BIBP3226 also non-specifically increased [S-35]GTPgammaS binding. The usefulness of BIBP3226 as an antagonist tool on the NPFF receptor is thus limited. (C) 2003 Elsevier lnc. All rights reserved.
引用
收藏
页码:1947 / 1954
页数:8
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