A REVIEW OF THE INVITRO AND INVIVO NEUROCHEMICAL CHARACTERIZATION OF THE NMDA PCP GLYCINE ION CHANNEL RECEPTOR MACROCOMPLEX

被引:45
|
作者
WOOD, PL
RAO, TS
IYENGAR, S
LANTHORN, T
MONAHAN, J
CORDI, A
SUN, E
VAZQUEZ, M
GRAY, N
CONTRERAS, P
机构
[1] CNS Diseases Research, G.D. Searle and Co., c/o Monsanto Co., St. Louis, 63198, MO
关键词
cerebellar cGMP; CGS; 19755; Glycine receptor; neural degeneration; NMDA; PCP; receptor coupling; stroke;
D O I
10.1007/BF00972212
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Current neurochemical studies of the NMDA receptor macromolecular complex are yielding new insights into the interactions of the subunits of this complex and the associated potential clinical benefits of selective modulation of these subnits. Such studies offer the great potential for a new generation of pharmacotherapies for a wide range of CNS disorders, including stroke, a condition for which there is currently no effective pharmacological treatment. However, it is essential to understand that the first generation products in this area may not be optimal pharmacotherapies, such that haracterization of possible receptor subtypes and understanding the molecular biology of the component proteins of the receptor complex will be crucial in the design of the optimal pharmacological modulators of the NMDA receptor complex. © 1990 Plenum Publishing Corporation.
引用
收藏
页码:217 / 230
页数:14
相关论文
共 50 条
  • [21] Synthesis and characterization of 4,6-dichloroindole-based radioligands for imaging the glycine site of the NMDA ion channel
    Waterhouse, RN
    Sultana, A
    Guo, N
    Lee, B
    Simpson, N
    Collier, L
    Laruelle, M
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2002, 45 (02): : 91 - 102
  • [22] PCP ANALOGS - SITE OF ACTION AT NMDA-TYPE RECEPTOR ASSOCIATED ION CHANNELS
    LEHMANN, J
    MCPHERSON, SE
    WOOD, PL
    CHENEY, DL
    CLINICAL NEUROPHARMACOLOGY, 1986, 9 : 497 - 499
  • [23] MODULATION OF SEIZURE SUSCEPTIBILITY IN THE MOUSE BY THE STRYCHNINE-INSENSITIVE GLYCINE RECOGNITION SITE OF THE NMDA RECEPTOR ION CHANNEL COMPLEX
    SINGH, L
    OLES, RJ
    TRICKLEBANK, MD
    BRITISH JOURNAL OF PHARMACOLOGY, 1990, 99 (02) : 285 - 288
  • [24] Analysis of the glycine binding domain of the NMDA receptor channel zeta 1 subunit
    Uchino, S
    NakajimaLijima, S
    Okuda, K
    Mishina, M
    Kawamoto, S
    NEUROREPORT, 1997, 8 (02) : 445 - 449
  • [25] Structure and function of GluN1-3A NMDA receptor excitatory glycine receptor channel
    Michalski, Kevin
    Furukawa, Hiro
    SCIENCE ADVANCES, 2024, 10 (15)
  • [26] Binding of ArgTX-636 in the NMDA Receptor Ion Channel
    Poulsen, Mette H.
    Andersen, Jacob
    Christensen, Rune
    Hansen, Kasper B.
    Traynelis, Stephen F.
    Stromgaard, Kristian
    Kristensen, Anders Skov
    JOURNAL OF MOLECULAR BIOLOGY, 2015, 427 (01) : 176 - 189
  • [27] NEUROCHEMICAL CHARACTERIZATION OF DOPAMINERGIC EFFECTS OF OPIPRAMOL, A POTENT SIGMA RECEPTOR LIGAND, INVIVO
    RAO, TS
    CLER, JA
    MICK, SJ
    DILWORTH, VM
    CONTRERAS, PC
    IYENGAR, S
    WOOD, PL
    NEUROPHARMACOLOGY, 1990, 29 (12) : 1191 - 1197
  • [28] NMDA RECEPTOR ANTAGONIST EFFECTS OF THE STEREOISOMERS OF BETA-CYCLAZOCINE IN RATS, INVIVO AND INVITRO
    CHURCH, J
    MILLAR, JD
    JONES, MG
    LODGE, D
    EUROPEAN JOURNAL OF PHARMACOLOGY, 1991, 192 (03) : 337 - 342
  • [29] POTENT INVITRO AND INVIVO ANTAGONISTS OF THE NMDA RECEPTOR AT THE GLYCINE SITE - 3-HYDROXY-2,5-DIOXO-1H-BENZ[B]AZEPINES
    CHAPDELAINE, MJ
    MCLAREN, CD
    WILDONGER, RA
    PULLAN, LM
    GOLDSTEIN, JM
    PATEL, JB
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1993, 205 : 83 - MEDI
  • [30] RPR-104632, A NOVEL GLYCINE ANTAGONIST OF THE NMDA RECEPTOR-CHANNEL COMPLEX
    MIGNANI, S
    BARREAU, M
    BLANCHARD, JC
    BOHME, A
    BOIREAU, A
    DOBLE, A
    RATAUD, J
    RANDLE, JCR
    SCHUMANN, P
    STUTZMANN, JM
    JIMONET, P
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1994, 208 : 167 - MEDI