Agonist-independent modulation of N-type calcium channels by ORL1 receptors

被引:110
作者
Beedle, AM
McRory, JE
Poirot, O
Doering, CJ
Altier, C
Barrere, C
Hamid, J
Nargeot, J
Bourinet, E
Zamponi, GW
机构
[1] Univ Calgary, Dept Physiol & Biophys, Cellular & Mol Neurobiol Res Grp, Calgary, AB T2N 4N1, Canada
[2] CNRS, UPR2580, LGF, Dept Physiol, F-34396 Montpellier, France
基金
加拿大健康研究院;
关键词
D O I
10.1038/nn1180
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have investigated modulation of voltage-gated calcium channels by nociceptin (ORL1) receptors. In rat DRG neurons and in tsA-201 cells, nociceptin mediated a pronounced inhibition of N-type calcium channels, whereas other calcium channel subtypes were unaffected. In tsA-201 cells, expression of N-type channels with human ORL1 resulted in a voltage-dependent G-protein inhibition of the channel that occurred in the absence of nociceptin, the ORL1 receptor agonist. Consistent with this observation, native N-type channels of small nociceptive dorsal root ganglion (DRG) neurons also had tonic inhibition by G proteins. Biochemical characterization showed the existence of an N-type calcium channel-ORL1 receptor signaling complex, which efficiently exposes N-type channels to constitutive ORL1 receptor activity. Calcium channel activity is thus regulated by changes in ORL1 receptor expression, which provides a possible molecular mechanism for the development of tolerance to opioid receptor agonists.
引用
收藏
页码:118 / 125
页数:8
相关论文
共 51 条
[1]  
Abdulla FA, 1997, J NEUROSCI, V17, P8721
[2]   The role of the ORL1 receptor in the modulation of spinal neurotransmission by nociceptin/orphanin FQ and nocistatin [J].
Ahmadi, S ;
Liebel, JT ;
Zeilhofer, HU .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 412 (01) :39-44
[3]   A putative α-helical Gβγ-coupling domain in the second intracellular loop of the 5-HT1A receptor [J].
Albert, PR ;
Morris, SJ ;
Ghahremani, MH ;
Storring, JM ;
Lembo, PMC .
ADVANCES IN SEROTONIN RECEPTOR RESEARCH: MOLECULAR BIOLOGY, SIGNAL TRANSDUCTION, AND THERAPEUTICS, 1998, 861 :146-161
[4]   Differential modulation of N-type α1B and P/Q-type α1A calcium channels by different G protein β subunit isoforms [J].
Arnot, MI ;
Stotz, SC ;
Jarvis, SE ;
Zamponi, GW .
JOURNAL OF PHYSIOLOGY-LONDON, 2000, 527 (02) :203-212
[5]   PERTUSSIS TOXIN AND VOLTAGE DEPENDENCE DISTINGUISH MULTIPLE PATHWAYS MODULATING CALCIUM CHANNELS OF RAT SYMPATHETIC NEURONS [J].
BEECH, DJ ;
BERNHEIM, L ;
HILLE, B .
NEURON, 1992, 8 (01) :97-106
[6]  
Beedle A. M., 2003, CALCIUM CHANNEL PHAR
[7]   Inhibition of transiently expressed low- and high-voltage-activated calcium channels by trivalent metal cations [J].
Beedle, AM ;
Hamid, J ;
Zamponi, GW .
JOURNAL OF MEMBRANE BIOLOGY, 2002, 187 (03) :225-238
[8]   Nociceptin and the ORL-1 ligand [Phe1ψ (CH2-NH)Gly2]nociceptin(1-13)NH2 exert anti-opioid effects in the Freund's adjuvant-induced arthritic rat model of chronic pain [J].
Bertorelli, R ;
Corradini, L ;
Rafiq, K ;
Tupper, J ;
Calò, G ;
Ongini, E .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 128 (06) :1252-1258
[9]   Nociceptin inhibits calcium channel currents in a subpopulation of small nociceptive trigeminal ganglion neurons in mouse [J].
Borgland, SL ;
Connor, M ;
Christie, MJ .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 536 (01) :35-47
[10]   Up-regulation of ORL-1 receptors in spinal tissue of allodynic rats after sciatic nerve injury [J].
Briscini, L ;
Corradini, L ;
Ongini, E ;
Bertorelli, R .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2002, 447 (01) :59-65