Bidirectional actions of nociceptin/orphanin FQ on Aδ-fibre-evoked responses in rat superficial spinal dorsal horn in vitro

被引:16
作者
Ruscheweyh, R [1 ]
Sandkühler, J [1 ]
机构
[1] Univ Heidelberg, Inst Physiol & Pathophysiol, D-69120 Heidelberg, Germany
关键词
nociception; analgesia; nocistatin; ORL-1; receptor; primary afferent; synaptic transmission;
D O I
10.1016/S0306-4522(01)00354-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The present study investigated the modulatory actions of nociceptin/orphanin FQ on excitatory glutamatergic transmission in spinal dorsal horn. In transverse spinal cord slices with an attached dorsal root, mono- and polysynaptic A delta -fibre-evoked extracellular field potentials were recorded from superficial dorsal horn. Nociceptin/orphanin FQ showed bidirectional effects on monosynaptic transmission with a potentiation at lower concentrations (100-300 nM) and a dose-dependent depression at higher concentrations (1-3 muM). The polysynaptic field potential was dose-dependently depressed by nociceptin/orphanin FQ (100 nM-3 muM). None of the actions of nociceptin/orphanin FQ was reversed by the nonspecific opioid receptor antagonist naloxone, the N-methyl-D-aspartate receptor antagonist D-2-amino-5-phosphonovaleric acid or the peptide nocistatin. The bidirectional actions of nociceptin/orphanin FQ on the monosynaptic field potential may provide an in vitro model for the bidirectional actions of nociceptin/orphanin FQ in behavioural studies showing hyperalgesia at low doses of intrathecal nociceptin/orphanin FQ and analgesia at higher doses. (C) 2001 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:275 / 281
页数:7
相关论文
共 44 条
[1]  
Anton B, 1996, J COMP NEUROL, V368, P229
[2]   Spinally delivered nociceptin/orphanin FQ reduces flinching behaviour in the rat formalin test [J].
Erb, K ;
Liebel, JT ;
Tegeder, I ;
Zeilhofer, HU ;
Brune, K ;
Geisslinger, G .
NEUROREPORT, 1997, 8 (08) :1967-1970
[3]   Depression of glutamatergic transmission by nociceptin in the neonatal rat hemisected spinal cord preparation in vitro [J].
Faber, ESL ;
Chambers, JP ;
Evans, RH ;
Henderson, G .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 119 (02) :189-190
[4]   Anti-hyperalgesic and anti-allodynic effects of intrathecal nociceptin/orphanin FQ in rats after spinal cord injury, peripheral nerve injury and inflammation [J].
Hao, JX ;
Xu, IS ;
Wiesenfeld-Hallin, Z ;
Xu, XJ .
PAIN, 1998, 76 (03) :385-393
[5]   Characterization of nociceptin hyperalgesia and allodynia in conscious mice [J].
Hara, N ;
Minami, T ;
OkudaAshitaka, E ;
Sugimoto, T ;
Sakai, M ;
Onaka, M ;
Mori, H ;
Imanishi, T ;
Shingu, K ;
Ito, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (03) :401-408
[6]   The orphan opioid receptor and its endogenous ligand-nociceptin/orphanin FQ [J].
Henderson, G ;
McKnight, AT .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1997, 18 (08) :293-300
[7]  
Inoue M, 1999, J PHARMACOL EXP THER, V291, P308
[8]   Nociceptin/orphanin FQ-induced nociceptive responses through substance P release from peripheral nerve endings in mice [J].
Inoue, M ;
Kobayashi, M ;
Kozaki, S ;
Zimmer, A ;
Ueda, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10949-10953
[9]  
Ito S, 2000, Prog Brain Res, V129, P205
[10]   Antinociceptive and morphine modulatory actions of spinal orphanin FQ [J].
Jhamandas, KH ;
Sutak, M ;
Henderson, G .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1998, 76 (03) :314-324