Neurotoxicity of glutamate at the concentration released upon spinal cord injury

被引:146
作者
Liu, D
Xu, GY
Pan, E
McAdoo, DJ [1 ]
机构
[1] Univ Texas, Med Branch, Inst Marine Biomed, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Dept Neurol, Galveston, TX 77555 USA
[3] Univ Texas, Med Branch, Dept Human Biol Chem & Genet, Galveston, TX 77555 USA
关键词
amino acid release; contusion model; excitotoxicity; microdialysis; rat; secondary damage;
D O I
10.1016/S0306-4522(99)00278-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Damage caused by administering glutamate into the spinal cord was characterized histologically. Glutamate destroyed neurons for several hundred micrometers around the administering microdiaIysis fiber. At 24h after treatment, significant (P = 0.036) loss of neurons was observed (75%) relative to control (47%) near the fiber when glutamate was administered for 1 h at a concentration outside the fiber approximating the maximum glutamate released upon spinal cord injury. Significant loss of neurons (P = 0.006, 0.022) was also caused by administering a combination of glutamate at about its average concentration released upon injury over the 1 h period of administration in combination with the maximum aspartate concentration released upon injury. This work provides a direct demonstration that the concentrations of excitatory amino acids released upon spinal cord injury are neurotoxic. The destruction of neurons by exposure to excitatory amino acids when there is also substantial loss of neurons simply from the presence of the microdialysis fiber may reflect sensitization of neurons to excitotoxicity by stress. (C) 1999 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:1383 / 1389
页数:7
相关论文
共 51 条
[1]  
Alessandri B, 1996, ACT NEUR S, V67, P6
[2]   ISCHEMIC DAMAGE IN HIPPOCAMPAL CA1 IS DEPENDENT ON GLUTAMATE RELEASE AND INTACT INNERVATION FROM CA3 [J].
BENVENISTE, H ;
JORGENSEN, MB ;
SANDBERG, M ;
CHRISTENSEN, T ;
HAGBERG, H ;
DIEMER, NH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1989, 9 (05) :629-639
[3]  
BULLER RE, 1993, POSTGRAD OBSTET GYNE, V13, P1
[4]   STEADY-STATE THEORY FOR QUANTITATIVE MICRODIALYSIS OF SOLUTES AND WATER INVIVO AND INVITRO [J].
BUNGAY, PM ;
MORRISON, PF ;
DEDRICK, RL .
LIFE SCIENCES, 1990, 46 (02) :105-119
[5]   ACUTE EFFECT OF ORAL AND SUBCUTANEOUS ADMINISTRATION OF MONOSODIUM GLUTAMATE ON ARCUATE NUCLEUS OF HYPOTHALAMUS IN MICE AND RATS [J].
BURDE, RM ;
SCHAINKER, B ;
KAYES, J .
NATURE, 1971, 233 (5314) :58-+
[6]   GLUTAMATE NEUROTOXICITY AND DISEASES OF THE NERVOUS-SYSTEM [J].
CHOI, DW .
NEURON, 1988, 1 (08) :623-634
[7]  
CHOI DW, 1987, J NEUROSCI, V7, P357
[9]   INSITU INJECTION OF KAINIC ACID - NEW METHOD FOR SELECTIVELY LESIONING NEURONAL CELL BODIES WHILE SPARING AXONS OF PASSAGE [J].
COYLE, JT ;
MOLLIVER, ME ;
KUHAR, MJ .
JOURNAL OF COMPARATIVE NEUROLOGY, 1978, 180 (02) :301-323
[10]   LESION OF STRIATAL NEURONS WITH KAINIC ACID PROVIDES A MODEL FOR HUNTINGTONS-CHOREA [J].
COYLE, JT ;
SCHWARCZ, R .
NATURE, 1976, 263 (5574) :244-246