STEROID-HORMONES PROTECT SPINAL-CORD NEURONS FROM GLUTAMATE TOXICITY

被引:106
作者
OGATA, T [1 ]
NAKAMURA, Y [1 ]
TSUJI, K [1 ]
SHIBATA, T [1 ]
KATAOKA, K [1 ]
机构
[1] EHIME UNIV,SCH MED,DEPT ORTHOPAED SURG,SHIGENOBU,EHIME 79102,JAPAN
关键词
D O I
10.1016/0306-4522(93)90513-F
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of steroid hormones on glutamate neurotoxicity were examined in cultured spinal cord neurons. The extent of neuronal damage, produced by glutamate exposure for 15 min, was estimated based on the activity of lactate dehydrogenase released from degenerated neurons to the media during 24 h of post-exposure incubation. This damage was dependent on the glutamate concentrations used. The addition of dexamethasone, a synthetic steroid, in post-exposure media remarkably reduced the extent of damage in a dose-dependent manner. The half effective concentration for the steroid was approximately 0.7 muM, which was in the range of pharmacological concentration. Dexamethasone was effective even when it was added 2 h after glutamate exposure. Some endogenous steroid hormones-aldosterone, progesterone and testosterone-also showed similar neuroprotective effects. However, cholesterol, a precursor of these steroid hormones, had no effect on glutamate neurotoxicity. This direct protective effect on neurons against glutamate neurotoxicity may explain, at least partly, the mechanisms of beneficial effects of steroid hormones on in vivo spinal cord injury.
引用
收藏
页码:445 / 449
页数:5
相关论文
共 19 条
[1]   CHOLECYSTOKININ-INDUCED PROTECTION OF CULTURED CORTICAL-NEURONS AGAINST GLUTAMATE NEUROTOXICITY [J].
AKAIKE, A ;
TAMURA, Y ;
SATO, Y ;
OZAKI, K ;
MATSUOKA, R ;
MIURA, S ;
YOSHINAGA, T .
BRAIN RESEARCH, 1991, 557 (1-2) :303-307
[2]   ELEVATION OF THE EXTRACELLULAR CONCENTRATIONS OF GLUTAMATE AND ASPARTATE IN RAT HIPPOCAMPUS DURING TRANSIENT CEREBRAL-ISCHEMIA MONITORED BY INTRACEREBRAL MICRODIALYSIS [J].
BENVENISTE, H ;
DREJER, J ;
SCHOUSBOE, A ;
DIEMER, NH .
JOURNAL OF NEUROCHEMISTRY, 1984, 43 (05) :1369-1374
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   GLUTAMATE NEUROTOXICITY IN CORTICAL CELL-CULTURE IS CALCIUM DEPENDENT [J].
CHOI, DW .
NEUROSCIENCE LETTERS, 1985, 58 (03) :293-297
[6]   DEVELOPMENTAL-CHANGE IN THE NERVE GROWTH-FACTOR ACTION FROM INDUCTION OF CHOLINE-ACETYLTRANSFERASE TO PROMOTION OF CELL-SURVIVAL IN CULTURED BASAL FOREBRAIN CHOLINERGIC NEURONS FROM POSTNATAL RATS [J].
HATANAKA, H ;
TSUKUI, H ;
NIHONMATSU, I .
DEVELOPMENTAL BRAIN RESEARCH, 1988, 39 (01) :85-95
[7]   PATHOGENESIS OF SPINAL-CORD INJURY AND NEWER TREATMENTS - A REVIEW [J].
JANSSEN, L ;
HANSEBOUT, RR .
SPINE, 1989, 14 (01) :23-32
[8]  
KHO JY, 1987, J NEUROSCI METH, V20, P83
[9]  
Kuchner EF, 1976, DYNAMICS BRAIN EDEMA, P315
[10]   NMDA-RECEPTOR ACTIVATION INCREASES CYTOPLASMIC CALCIUM-CONCENTRATION IN CULTURED SPINAL-CORD NEURONS [J].
MACDERMOTT, AB ;
MAYER, ML ;
WESTBROOK, GL ;
SMITH, SJ ;
BARKER, JL .
NATURE, 1986, 321 (6069) :519-522