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

机译:Pfr(Tic)amide和BIBP3226在人神经肽FF2受体上的功能特性。

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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 [35S]guanosine-5'-O-(3-thio)triphosphate ([35S]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 [35S]GTP-gammaS binding. The usefulness of BIBP3226 as an antagonist tool on the NPFF receptor is thus limited.
机译:研究了两种假定的神经肽FF(NPFF)拮抗剂BIBP3226和PFR(Tic)酰胺对人神经肽FF受体亚型2(hNPFF2)的功能特性。令人惊讶地,在[35S]鸟苷-5'-O-(3-硫代)三磷酸酯([35S]GTPγS)结合测定中,PFR(Tic)酰胺显示出激动剂特性。 PFR(Tic)酰胺的疗效显着高于NPFF的稳定类似物(1DMe)Y8Fa,因此PFR(Tic)酰胺可归类为“超激动剂”。 BIBP3226确实充当了hNPFF2受体的可逆竞争拮抗剂。但是,高浓度的BIBP3226也非特异性地增加了[35S]GTP-γS的结合。因此限制了BIBP3226作为NPFF受体上的拮抗剂工具的用途。

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