Modification of dopamine release by nociceptin in conscious rat striatum

被引:32
作者
Konya, H
Masuda, H
Itoh, K
Nagai, K
Kakishita, E
Matsuoka, A
机构
[1] Hyogo Coll Med, Dept Clin Labs, Nishinomiya, Hyogo 6638501, Japan
[2] Hyogo Coll Med, Dept Pharmacol, Nishinomiya, Hyogo 6638501, Japan
[3] Hyogo Coll Med, Dept Internal Med 2, Nishinomiya, Hyogo 6638501, Japan
[4] Hyogo Coll Med, Dept Clin Pathol, Nishinomiya, Hyogo 6638501, Japan
关键词
nociceptin; orphanin FQ; microdialysis; striatum; dopamine; naloxone;
D O I
10.1016/S0006-8993(98)00075-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nociceptin (NOC), an endogenous ligand for the orphan receptor ORL1, has recently been recognized as a neuropeptide. We used brain microdialysis and on-line high performance liquid chromatography to examine the effect of NOC on the basal outflow of dopamine (DA) and its metabolite in the freely moving rat striatum in vivo. The percent change of DA release induced by NOC at concentrations of 10(-6) and 10(-5) M were 383% and 398%, respectively. This effect of NOC was attenuated by naloxone, suggesting that NOC activates classic (mu, delta, kappa) receptors in a very little way. These data indicates that NOC may act as a neuropeptide which enhances DA release from the striatum of rat brain via an opioid receptor. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:341 / 344
页数:4
相关论文
共 25 条
[1]  
Anton B, 1996, J COMP NEUROL, V368, P229
[2]   MOLECULAR-CLONING AND TISSUE DISTRIBUTION OF A PUTATIVE MEMBER OF THE RAT OPIOID RECEPTOR GENE FAMILY THAT IS NOT A MU-OPIOID, DELTA-OPIOID OR KAPPA-OPIOID RECEPTOR-TYPE [J].
BUNZOW, JR ;
SAEZ, C ;
MORTRUD, M ;
BOUVIER, C ;
WILLIAMS, JT ;
LOW, M ;
GRANDY, DK .
FEBS LETTERS, 1994, 347 (2-3) :284-288
[3]   MOLECULAR-CLONING, TISSUE DISTRIBUTION AND CHROMOSOMAL LOCALIZATION OF A NOVEL MEMBER OF THE OPIOID RECEPTOR GENE FAMILY [J].
CHEN, Y ;
FAN, Y ;
LIU, J ;
MESTEK, A ;
TIAN, MT ;
KOZAK, CA ;
YU, L .
FEBS LETTERS, 1994, 347 (2-3) :279-283
[4]   The effect of nociceptin on Ca2+ channel current and intracellular Ca2+ in the SH-SY5Y human neuroblastoma cell line [J].
Connor, M ;
Yeo, A ;
Henderson, G .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 118 (02) :205-207
[5]  
DICHIARA G, 1988, J PHARMACOL EXP THER, V244, P1067
[6]   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
[7]   Nociceptin stimulates locomotion and exploratory behaviour in mice [J].
Florin, S ;
Suaudeau, C ;
Meunier, JC ;
Costentin, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 317 (01) :9-13
[8]   Modulation of enkephalin release by nociceptin (orphanin FQ) [J].
Gintzler, AR ;
Adapa, ID ;
Toll, L ;
Medina, VM ;
Wang, L .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1997, 325 (01) :29-34
[9]   Inhibition of tachykinin release from peripheral endings of sensory nerves by nociceptin, a novel opioid peptide [J].
Giuliani, S ;
Maggi, CA .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 118 (07) :1567-1569
[10]  
ILLES P, 1991, NEUROBIOLOGY OPIOIDS, P213