N-methyl-D-aspartate receptor blockade enhances neuronal apoptosis induced by serum deprivation

被引:25
作者
Terro, F [1 ]
Esclaire, F [1 ]
Yardin, C [1 ]
Hugon, J [1 ]
机构
[1] Fac Med Limoges, Dept Histol & Cell Biol, F-87025 Limoges, France
关键词
apoptosis; N-methyl-D-aspartate; neuron; (5R,10S)-(+)-5-methyl-10,11-dihydro-5H-dibenzo [a,d] cyclohepten-5,10-imine; hydrogen maleate; 2-amino-7-phosphonoheptanoic acid;
D O I
10.1016/S0304-3940(99)00911-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuronal apoptosis a hallmark of brain development could also be involved in neurodegenerative diseases. Glutamate toxicity is widely proposed as an important factor in the pathogenesis of neurological disorders. We show here that, in rat primary cortical cultures, the blockade of N-methyl-D-aspartate (NMDA) glutamate receptors exacerbated neuronal apoptosis induced by serum deprivation. This effect is observed at early stage of cultures (9 days in vitro (DIV)) and mildly decreases in more mature cultures (13 and 15 DIV). At the opposite, low concentrations of NMDA (5 mu M) or glutamate (5 mu M) prevented the neuronal apoptosis induced by trophic support withdrawal. In primary cortical cu Itu res, the proapoptotic effect of trophic support removal can be modulated by NMDA receptors depending upon the magnitude of these glutamate receptor activation. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:149 / 152
页数:4
相关论文
共 27 条
[1]  
Atabay C, 1996, J NEUROSCI RES, V43, P465
[2]   STRUCTURE-ACTIVITY ANALYSIS OF BINDING-KINETICS FOR NMDA RECEPTOR COMPETITIVE ANTAGONISTS - THE INFLUENCE OF CONFORMATIONAL RESTRICTION [J].
BENVENISTE, M ;
MAYER, ML .
BRITISH JOURNAL OF PHARMACOLOGY, 1991, 104 (01) :207-221
[3]   APOPTOSIS AND NECROSIS - 2 DISTINCT EVENTS INDUCED, RESPECTIVELY, BY MILD AND INTENSE INSULTS WITH N-METHYL-D-ASPARTATE OR NITRIC-OXIDE SUPEROXIDE IN CORTICAL CELL-CULTURES [J].
BONFOCO, E ;
KRAINC, D ;
ANKARCRONA, M ;
NICOTERA, P ;
LIPTON, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7162-7166
[4]   Ischemia-induced neuronal apoptosis [J].
Choi, DW .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (05) :667-672
[5]  
CHOI DW, 1987, J NEUROSCI, V7, P369
[6]  
COPANI A, 1995, MOL PHARMACOL, V47, P890
[7]   OXIDATIVE STRESS, GLUTAMATE, AND NEURODEGENERATIVE DISORDERS [J].
COYLE, JT ;
PUTTFARCKEN, P .
SCIENCE, 1993, 262 (5134) :689-695
[8]   GLUTAMATE-INDUCED NEURONAL DEATH IN CEREBELLAR CULTURE IS MEDIATED BY 2 DISTINCT COMPONENTS - A SODIUM-CHLORIDE COMPONENT AND A CALCIUM COMPONENT [J].
DESSI, F ;
CHARRIAUTMARLANGUE, C ;
BENARI, Y .
BRAIN RESEARCH, 1994, 650 (01) :49-55
[9]  
DESSI F, 1993, J NEUROCHEM, V60, P1955
[10]   Slowly triggered excitotoxicity occurs by necrosis in cortical cultures [J].
Gwag, BJ ;
Koh, JY ;
Demaro, JA ;
Ying, HS ;
Jacquin, M ;
Choi, DW .
NEUROSCIENCE, 1997, 77 (02) :393-401