Voltage-sensitivity at the human dopamine D2S receptor is agonist-specific

被引:25
作者
Sahlholm, Kristoffer [1 ]
Marcellino, Daniel [1 ]
Nilsson, Johanna [1 ]
Fuxe, Kjell [1 ]
Arhem, Peter [1 ]
机构
[1] Karolinska Inst, Dept Neurosci, SE-17177 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Dopamine D-2 receptor; Dopamine agonists; Voltage-sensitivity; Voltage-clamp; G protein-coupled receptor; Xenopus oocytes; Phenethylamines; Aminotetralins;
D O I
10.1016/j.bbrc.2008.10.117
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
Recently, we and others have shown that agonist potencies at some, but not all, G protein-coupled receptors are voltage-sensitive. Several of those studies employed electrophysiology assays in Xenopus oocytes with G protein-coupled potassium channels as a readout. Using this assay, we have now obtained evidence that voltage-sensitivity at the dopaamine D-2S receptor is agonist-specific. Whereas the potency of dopamine at the D-2S receptor is decreased by depolarization, the potencies of beta-phenethylamine, p(-) and m-tyramine are voltage-insensitive. Furthermore, both monohydroxylated and non-hydroxylated N,N-dipropyl-2-aminotetralin Compounds are voltage-sensitive. Differential activation of G protein subtypes or differential ratios between effector and active G protein do not underlie this agonist-selective voltage-sensitivity. This is the first demonstration of voltage-sensitive and voltage-insensitive behaviour of different agonists acting via the same receptor. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1216 / 1221
页数:6
相关论文
共 17 条
[1]   The M2 muscarinic G-protein-coupled receptor is voltage-sensitive [J].
Ben-Chaim, Y ;
Tour, O ;
Dascal, N ;
Parnas, I ;
Parnas, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (25) :22482-22491
[2]   Movement of 'gating charge' is coupled to ligand binding in a G-protein-coupled receptor [J].
Ben-Chaim, Yair ;
Chanda, Baron ;
Dascal, Nathan ;
Bezanilla, Francisco ;
Parnas, Itzchak ;
Parnas, Hanna .
NATURE, 2006, 444 (7115) :106-109
[3]   The mysterious trace amines: Protean neuromodulators of synaptic transmission in mammalian brain [J].
Burchett, Scott A. ;
Hicks, T. Philip .
PROGRESS IN NEUROBIOLOGY, 2006, 79 (5-6) :223-246
[4]   Effect of multiple serine/alanine mutations in the transmembrane spanning region V of the D2 dopamine receptor on ligand binding [J].
Coley, C ;
Woodward, R ;
Johansson, AM ;
Strange, PG ;
Naylor, LH .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (01) :358-366
[5]   CONTRIBUTIONS OF CONSERVED SERINE RESIDUES TO THE INTERACTIONS OF LIGANDS WITH DOPAMINE-D2 RECEPTORS [J].
COX, BA ;
HENNINGSEN, RA ;
SPANOYANNIS, A ;
NEVE, RL ;
NEVE, KA .
JOURNAL OF NEUROCHEMISTRY, 1992, 59 (02) :627-635
[6]   Activation of G Protein Coupled Receptors [J].
Deupi, Xavier ;
Kobilka, Brian .
MECHANISMS AND PATHWAYS OF HETEROTRIMERIC G PROTEIN SIGNALING, 2007, 74 :137-166
[7]   Dopamine receptor microdomains involved in molecular recognition and the regulation of drug affinity and function [J].
Floresea, CZ ;
Schetz, JA .
JOURNAL OF RECEPTORS AND SIGNAL TRANSDUCTION, 2004, 24 (03) :207-239
[8]  
KENAKIN TP, 1984, PHARMACOL REV, V36, P165
[9]   G protein coupling and ligand selectivity of the D2L and D3 dopamine receptors [J].
Lane, J. Robert ;
Powney, Ben ;
Wise, Alan ;
Rees, Stephen ;
Milligan, Graeme .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2008, 325 (01) :319-330
[10]   A role for membrane potential in regulating GPCRs? [J].
Mahaut-Smith, Martyn P. ;
Martinez-Pinna, Juan ;
Gurung, Iman S. .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2008, 29 (08) :421-429