NMDA receptor antagonists as analgesics: focus on the NR2B subtype

被引:172
作者
Chizh, BA
Headley, PM
Tzschentke, TM
机构
[1] Grunenthal GMBH Res & Dev, Dept Pharmacol, D-52078 Aachen, Germany
[2] Univ Bristol, Dept Physiol, Bristol BS8 1TD, Avon, England
关键词
D O I
10.1016/S0165-6147(00)01863-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ifenprodil and a group of related compounds are selective antagonists of NR2B-containing NMDA receptors. These compounds are antinociceptive in a variety of preclinical pain models and have a much lower side-effect profile compared with other NMDA receptor antagonists. It remains unclear whether the improved safety of these compounds is due to their subtype selectivity or to a unique mode of inhibition of the receptor. Human trials have so far confirmed the good tolerability of these subtype-selective NMDA receptor antagonists; however, whether they are as effective as other NMDA receptor antagonists in pain patients remains to be demonstrated.
引用
收藏
页码:636 / 642
页数:7
相关论文
共 54 条
[1]   EVALUATION OF THE REINFORCING EFFECTS OF ELIPRODIL IN RHESUS-MONKEYS AND ITS DISCRIMINATIVE STIMULUS EFFECTS IN RATS [J].
BALSTER, RL ;
NICHOLSON, KL ;
SANGER, DJ .
DRUG AND ALCOHOL DEPENDENCE, 1994, 35 (03) :211-216
[2]  
BEARDSLEY PM, 1990, J PHARMACOL EXP THER, V252, P953
[3]   Blockade of the polyamine site of NMDA receptors produces antinociception and enhances the effect of morphine, in mice [J].
Bernardi, M ;
Bertolini, A ;
Szczawinska, K ;
Genedani, S .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 298 (01) :51-55
[4]   Selective NMDA NR2B antagonists induce antinociception without motor dysfunction: correlation with restricted localisation of NR2B subunit in dorsal horn [J].
Boyce, S ;
Wyatt, A ;
Webb, JK ;
O'Donnell, R ;
Mason, G ;
Rigby, M ;
Sirinathsinghji, D ;
Hill, RG ;
Rupniak, NMJ .
NEUROPHARMACOLOGY, 1999, 38 (05) :611-623
[6]  
Carlton S M, 2001, Curr Opin Pharmacol, V1, P52, DOI 10.1016/S1471-4892(01)00002-9
[7]  
CARTER RB, 2000, SOC NEUR ABSTR, V26
[8]   (1S,2S)-1-(4-HYDROXYPHENYL)-2-(4-HYDROXY-4-PHENYLPIPERIDINO)-1-PROPANOL - A POTENT NEW NEUROPROTECTANT WHICH BLOCKS N-METHYL-D-ASPARTATE RESPONSES [J].
CHENARD, BL ;
BORDNER, J ;
BUTLER, TW ;
CHAMBERS, LK ;
COLLINS, MA ;
DECOSTA, DL ;
DUCAT, MF ;
DUMONT, ML ;
FOX, CB ;
MENA, EE ;
MENNITI, FS ;
NIELSEN, J ;
PAGNOZZI, MJ ;
RICHTER, KEG ;
RONAU, RT ;
SHALABY, IA ;
STEMPLE, JZ ;
WHITE, WF .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (16) :3138-3145
[9]  
Chenard BL, 1999, CURR PHARM DESIGN, V5, P381
[10]   Stimulus intensity, cell excitation and the N-methyl-D-aspartate receptor component of sensory responses in the rat spinal cord in vivo [J].
Chizh, BA ;
Cumberbatch, MJ ;
Herrero, JF ;
Stirk, GC ;
Headley, PM .
NEUROSCIENCE, 1997, 80 (01) :251-265