Role of cyclic GMP in glutamate neurotoxicity in primary cultures of cerebellar neurons

被引:52
作者
Montoliu, C [1 ]
Llansola, M [1 ]
Kosenko, E [1 ]
Corbalán, R [1 ]
Felipo, V [1 ]
机构
[1] Fdn Valenciana Invest Biomed, Inst Invest Citol, Valencia 46010, Spain
关键词
cyclic GMP; glutamate; neurotoxicity; guanylate cyclase; phosphodiesterase; neuroprotection;
D O I
10.1016/S0028-3908(99)00071-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The role of cGMP in the mediation of glutamate neurotoxicity remains controversial. Some reports indicate that cGMP mediates glutamate neurotoxicity while others indicate that cGMP is neuroprotective. We have studied the role of cGMP in the mediation of glutamate and nitric oxide neurotoxicity in primary cultures of cerebellar neurons. Inhibition of soluble guanylate cyclase prevents glutamate and nitric oxide neurotoxicity. There is a good correlation between inhibition of cGMP formation and neuroprotection. Moreover 8-Br-cGMP, a cell permeable analog of cGMP, induced neuronal death. These results indicate that increased intracellular cGMP is involved in the mechanism of neurotoxicity. Inhibitors of phosphodiesterase did not increase intracellular cGMP but increased the content of cGMP in the extracellular medium and prevented glutamate neurotoxicity. Moreover, addition of cGMP to the extracellular medium also prevented glutamate neurotoxicity in cerebellar neurons in culture. These results are compatible with a neurotoxic effect of increased intracellular cGMP and a neuroprotective effect of increased extracellular cGMP. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1883 / 1891
页数:9
相关论文
共 27 条
[1]   RETINAL DEGENERATION IN THE RD MOUSE IS CAUSED BY A DEFECT IN THE BETA-SUBUNIT OF ROD CGMP-PHOSPHODIESTERASE [J].
BOWES, C ;
LI, TS ;
DANCIGER, M ;
BAXTER, LC ;
APPLEBURY, ML ;
FARBER, DB .
NATURE, 1990, 347 (6294) :677-680
[2]   NITRIC-OXIDE MEDIATES GLUTAMATE-LINKED ENHANCEMENT OF CGMP LEVELS IN THE CEREBELLUM [J].
BREDT, DS ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :9030-9033
[3]   SUPEROXIDE AND NITRIC-OXIDE COOPERATION IN HYPOXIA REOXYGENATION-INDUCED NEURON INJURY [J].
CAZEVIEILLE, C ;
MULLER, A ;
MEYNIER, F ;
BONNE, C .
FREE RADICAL BIOLOGY AND MEDICINE, 1993, 14 (04) :389-395
[4]  
CHOI DW, 1987, J NEUROSCI, V7, P369
[5]  
Cucarella C, 1998, J NEUROCHEM, V70, P1609
[6]  
DAWSON VL, 1993, J NEUROSCI, V13, P2651
[7]   NITRIC-OXIDE MEDIATES GLUTAMATE NEUROTOXICITY IN PRIMARY CORTICAL CULTURES [J].
DAWSON, VL ;
DAWSON, TM ;
LONDON, ED ;
BREDT, DS ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (14) :6368-6371
[8]   NANOMOLAR N-G-NITROARGININE INHIBITS NMDA-INDUCED CYCLIC-GMP FORMATION IN RAT CEREBELLUM [J].
EAST, SJ ;
GARTHWAITE, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 184 (2-3) :311-313
[9]   INHIBITORS OF PROTEIN-KINASE-C PREVENT THE TOXICITY OF GLUTAMATE IN PRIMARY NEURONAL CULTURES [J].
FELIPO, V ;
MINANA, MD ;
GRISOLIA, S .
BRAIN RESEARCH, 1993, 604 (1-2) :192-196
[10]  
Forloni G, 1997, J NEUROCHEM, V68, P319