THE ANTICONVULSANT ACTION OF CI-977, A SELECTIVE KAPPA-OPIOID RECEPTOR AGONIST - A POSSIBLE INVOLVEMENT OF THE GLYCINE NMDA RECEPTOR COMPLEX

被引:28
作者
SINGH, L
VASS, CA
HUNTER, JC
WOODRUFF, GN
HUGHES, J
机构
[1] Parke-Davis Research Unit, Addenbrookes Hospital Site, Cambridge, CB2 2QB, Hills Road
关键词
KAPPA-OPIOID RECEPTORS; GLYCINE/NMDA RECEPTORS; NMDLA (N-METHYL-DL-ASPARTATE); NMDLA INFUSION; SEIZURES;
D O I
10.1016/0014-2999(90)94183-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The selective kappa-opioid receptor agonist CI-977, stereoselectively antagonised clonic seizures induced by slow i.v. infusion of N-methyl-DL-aspartate in the mouse. It was found to be more efficacious and 10-fold more potent than the competitive N-methyl-D-aspartic acid receptor antagonist CPP (3-(+/-)-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid). The anticonvulsant action of CI-977 was antagonised by norbinaltorphimine, indicating a specific interaction with the kappa-receptor. The effect of CI-977 but not that of CPP was also antagonised by the glycine/NMDA receptor agonist D-serine. These results provide evidence for a possible interaction between the kappa-receptor and the glycine/NMDA receptor.
引用
收藏
页码:477 / 480
页数:4
相关论文
共 10 条
[1]  
BOYLE S J, 1990, Molecular Neuropharmacology, V1, P23
[2]   THE NOVEL ANTICONVULSANT MK-801 BINDS TO THE ACTIVATED STATE OF THE N-METHYL-D-ASPARTATE RECEPTOR IN RAT-BRAIN [J].
FOSTER, AC ;
WONG, EHF .
BRITISH JOURNAL OF PHARMACOLOGY, 1987, 91 (02) :403-409
[3]  
HUNTER JC, IN PRESS BR J PHARM
[4]   7-CHLOROKYNURENIC ACID IS A SELECTIVE ANTAGONIST AT THE GLYCINE MODULATORY SITE OF THE N-METHYL-D-ASPARTATE RECEPTOR COMPLEX [J].
KEMP, JA ;
FOSTER, AC ;
LEESON, PD ;
PRIESTLEY, T ;
TRIDGETT, R ;
IVERSEN, LL ;
WOODRUFF, GN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (17) :6547-6550
[5]  
MURPHY DE, 1987, J PHARMACOL EXP THER, V240, P778
[6]   MODULATION OF SEIZURE SUSCEPTIBILITY IN THE MOUSE BY THE STRYCHNINE-INSENSITIVE GLYCINE RECOGNITION SITE OF THE NMDA RECEPTOR ION CHANNEL COMPLEX [J].
SINGH, L ;
OLES, RJ ;
TRICKLEBANK, MD .
BRITISH JOURNAL OF PHARMACOLOGY, 1990, 99 (02) :285-288
[7]   ENANTIOMERS OF HA-966 (3-AMINO-1-HYDROXYPYRROLID-2-ONE) EXHIBIT DISTINCT CENTRAL NERVOUS-SYSTEM EFFECTS - (+)-HA-966 IS A SELECTIVE GLYCINE N-METHYL-D-ASPARTATE RECEPTOR ANTAGONIST, BUT (-)-HA-966 IS A POTENT GAMMA-BUTYROLACTONE-LIKE SEDATIVE [J].
SINGH, L ;
DONALD, AE ;
FOSTER, AC ;
HUTSON, PH ;
IVERSEN, LL ;
IVERSEN, SD ;
KEMP, JA ;
LEESON, PD ;
MARSHALL, GR ;
OLES, RJ ;
PRIESTLEY, T ;
THORN, L ;
TRICKLEBANK, MD ;
VASS, CA ;
WILLIAMS, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :347-351
[8]  
TORTELLA FC, 1986, J PHARMACOL EXP THER, V237, P49
[9]  
TORTELLA FC, 1990, LIFE SCI, V46, P1
[10]  
VONVOIGTLANDER PF, 1987, J PHARMACOL EXP THER, V243, P542