Inhibition of NMDA-induced currents by conantokin-G and conantokin-T in cultured embryonic murine hippocampal neurons

被引:23
作者
Klein, RC
Galdzicki, Z
Castellino, FJ [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
[2] NIA, Neurosci Lab, NIH, Bethesda, MD 20892 USA
关键词
N-methyl-D-aspartate receptor; conantokins; electrophysiology; polyamines; hippocampal neurons;
D O I
10.1016/S0028-3908(99)00065-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Conantokin-G (con-G) and conantokin-T (con-T) are small (17 and 21 amino acids, respectively) gamma-carboxyglutamate (Gla) containing peptides derived from the venoms of marine cone snails that are potent and selective inhibitors of N-methyl-D-aspartate (NMDA) receptors. In this study, the effects of con-G and con-T on NMDA-evoked responses were evaluated in mouse primary hippocampal neuronal cultures using the whole-cell patch-clamp technique. Under equilibrium conditions, NMDA-induced currents were inhibited by con-G and con-T (10 nM-100 mu M) in a dose-dependent manner while maintaining a holding potential of -70 mV. In the presence of saturating amounts of NMDA (100 mu M) and glycine (1 mu M), the IC50 values obtained were 487 +/- 85 nM for con-G and 1030 +/- 130 nM for con-T. NMDA (10 mu M-1 mM) dose-response curves produced in the presence of con-G or con-T (1 or 3 mu M) resulted in a downward shift of the current response at saturation with NMDA, without affecting the EC,,. The maximum response obtainable in the absence of peptide could not be achieved by increasing concentrations of NMDA. The same effect was also observed for conantokin inhibition of spermine-potentiated responses. Association rate constants (k(on)) for the peptides were determined in the presence of NMDA and glycine, with and without the addition of spermine. Using a single binding site bimolecular model, k(on) values were 3.1 +/- 0.2 x 10(3) M-1 s(-1) for con-G and 3.2 +/- 0.1 x 103 M-1 s(-1) for con-T in the absence of spermine. The added presence of a saturating amount of spermine (300 mu M) resulted in an approximate 60% increase in the k(on) values for both con-G and con-T. These results demonstrate that con-T and con-G inhibit NMDA-evoked currents, as well as the potentiation by spermine, in what appears to be a noncompetitive manner, and that spermine increases the rate of conantokin inhibition. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1819 / 1829
页数:11
相关论文
共 43 条
[1]   SELECTIVE MODULATION OF NMDA RESPONSES BY REDUCTION AND OXIDATION [J].
AIZENMAN, E ;
LIPTON, SA ;
LORING, RH .
NEURON, 1989, 2 (03) :1257-1263
[2]   N-METHYL-D-ASPARTATE RECEPTORS ARE CLUSTERED AND IMMOBILIZED ON DENDRITES OF LIVING CORTICAL-NEURONS [J].
BENKE, TA ;
JONES, OT ;
COLLINGRIDGE, GL ;
ANGELIDES, KJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) :7819-7823
[3]   MULTIPLE EFFECTS OF SPERMINE ON N-METHYL-D-ASPARTIC ACID RECEPTOR RESPONSES OF RAT CULTURED HIPPOCAMPAL-NEURONS [J].
BENVENISTE, M ;
MAYER, ML .
JOURNAL OF PHYSIOLOGY-LONDON, 1993, 464 :131-163
[4]   Metal-ion-binding properties of synthetic conantokin-G [J].
Blandl, T ;
Zajicek, J ;
Prorok, M ;
Castellino, FJ .
BIOCHEMICAL JOURNAL, 1997, 328 :777-783
[5]   A SYNAPTIC MODEL OF MEMORY - LONG-TERM POTENTIATION IN THE HIPPOCAMPUS [J].
BLISS, TVP ;
COLLINGRIDGE, GL .
NATURE, 1993, 361 (6407) :31-39
[6]  
CHANDLER P, 1993, J BIOL CHEM, V268, P17173
[7]   Conformational changes in conantokin-G induced upon binding of calcium and magnesium as revealed by NMR structural analysis [J].
Chen, ZG ;
Blandl, T ;
Prorok, M ;
Warder, SE ;
Li, LP ;
Zhu, Y ;
Pedersen, LG ;
Ni, F ;
Castellino, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (26) :16248-16258
[8]  
CHRISTINE CW, 1990, J NEUROSCI, V10, P108
[9]   PHENCYCLIDINE AND RELATED DRUGS BIND TO THE ACTIVATED N-METHYL-D-ASPARTATE RECEPTOR CHANNEL COMPLEX IN RAT-BRAIN MEMBRANES [J].
FAGG, GE .
NEUROSCIENCE LETTERS, 1987, 76 (02) :221-227
[10]   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