DIFFERENTIAL TEMPORAL PATTERNS OF EXPRESSION OF IMMEDIATE-EARLY GENES IN CEREBRAL-CORTEX INDUCED BY INTRACEREBRAL EXCITOTOXIN INJECTION - SENSITIVITY TO DEXAMETHASONE AND MK-801

被引:8
作者
COLLACOMORAES, Y [1 ]
DEBELLEROCHE, J [1 ]
机构
[1] CHARING CROSS & WESTMINSTER MED SCH,DEPT BIOCHEM,LONDON W6 8RF,ENGLAND
关键词
IMMEDIATE EARLY GENES; MESSENGER RNA; GLUTAMATE RECEPTORS; MK-801; C-FOS; C-JUN; ZIF-268;
D O I
10.1016/0028-3908(95)00021-W
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A number of conditions associated with persistent excitation such as electrically and chemically-induced seizures cause a rapid increase in the expression of immediate early genes (IEG) such as c-fos. In this study the time-course of induction of c-jun, jun-B and zif ?268 mRNA by kainate was characterized in rat cerebral cortex and compared to that of c-fos mRNA induction. Unilateral injection of kainate. into the nucleus basalis caused a significant induction of c-jun mRNA in cerebral cortex from 4 hr which was maximal at 8 hr, being 3 times greater in ipsilateral cortex than in control cortex. This pattern was also shown for jun-B and was similar, but of small magnitude, to that obtained with c-fos mRNA, with a maximal increase at 8 hr, whilst the maximal induction of zif-268 mRNA preceded these responses occurring at 4 hr. A marked difference was seen in duration in the c-jun induction which was maintained at a high level for at least 24 hr. Treatment of animals with MK-801 (within 30 min of injection of kainate) or dexamethasone (2-30 mg/kg) at the time of kainate injection significantly attenuated the response. The induction of c-fos mRNA by kainate injection was most sensitive to dexamethasone (2 mg/kg), whereas a higher dose (30 mg/kg) was required to attenuate the induction of zif-268 mRNA. These results show that a time-dependent and co-ordinated induction of c-fos, c-jun, jun-B and zif-268 mRNA in cerebral cortex occurs in response to the persistent excitation caused by excitotoxin injection which is mediated by glutamate and shows a differential sensitivity to dexamethasone.
引用
收藏
页码:521 / 531
页数:11
相关论文
共 73 条
[1]   ADRENALECTOMY ATTENUATES KAINIC ACID-ELICITED INCREASES OF MESSENGER-RNAS FOR NEUROTROPHINS AND THEIR RECEPTORS IN THE RAT-BRAIN [J].
BARBANY, G ;
PERSSON, H .
NEUROSCIENCE, 1993, 54 (04) :909-922
[2]   GROWTH-FACTORS AND MEMBRANE DEPOLARIZATION ACTIVATE DISTINCT PROGRAMS OF EARLY RESPONSE GENE-EXPRESSION - DISSOCIATION OF FOS AND JUN INDUCTION [J].
BARTEL, DP ;
SHENG, M ;
LAU, LF ;
GREENBERG, ME .
GENES & DEVELOPMENT, 1989, 3 (03) :304-313
[3]  
BAUDRY M, 1986, J NEUROSCI, V6, P3430
[4]   WIDESPREAD INCREASE OF NERVE GROWTH-FACTOR PROTEIN IN THE RAT FOREBRAIN AFTER KINDLING-INDUCED SEIZURES [J].
BENGZON, J ;
SODERSTROM, S ;
KOKAIA, Z ;
KOKAIA, M ;
ERNFORS, P ;
PERSSON, H ;
EBENDAL, T ;
LINDVALL, O .
BRAIN RESEARCH, 1992, 587 (02) :338-342
[5]   ACTIVATION OF THE ZINC FINGER ENCODING GENE KROX-20 IN ADULT-RAT BRAIN - COMPARISON WITH ZIF268 [J].
BHAT, RV ;
WORLEY, PF ;
COLE, AJ ;
BARABAN, JM .
MOLECULAR BRAIN RESEARCH, 1992, 13 (03) :263-266
[6]   LIPOCORTIN-1 INHIBITS NMDA RECEPTOR-MEDIATED NEURONAL DAMAGE IN THE STRIATUM OF THE RAT [J].
BLACK, MD ;
CAREY, F ;
CROSSMAN, AR ;
RELTON, JK ;
ROTHWELL, NJ .
BRAIN RESEARCH, 1992, 585 (1-2) :135-140
[7]   INHIBITION OF PHOSPHOLIPASE [J].
BLACKWELL, GJ ;
FLOWER, RJ .
BRITISH MEDICAL BULLETIN, 1983, 39 (03) :260-264
[8]   JUN-B DIFFERS IN ITS BIOLOGICAL PROPERTIES FROM, AND IS A NEGATIVE REGULATOR OF, C-JUN [J].
CHIU, R ;
ANGEL, P ;
KARIN, M .
CELL, 1989, 59 (06) :979-986
[9]   THE C-FOS PROTEIN INTERACTS WITH C-JUN/AP-1 TO STIMULATE TRANSCRIPTION OF AP-1 RESPONSIVE GENES [J].
CHIU, R ;
BOYLE, WJ ;
MEEK, J ;
SMEAL, T ;
HUNTER, T ;
KARIN, M .
CELL, 1988, 54 (04) :541-552
[10]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2