INDUCTION OF C-FOS MESSENGER-RNA EXPRESSION BY AFTERDISCHARGE IN THE HIPPOCAMPUS OF NAIVE AND KINDLED RATS

被引:123
作者
SHIN, C
MCNAMARA, JO
MORGAN, JI
CURRAN, T
COHEN, DR
机构
[1] DUKE UNIV,MED CTR,DEPT MED NEUROL,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DEPT PHARMACOL,DURHAM,NC 27710
[3] ROCHE INST MOLEC BIOL,ROCHE RES CTR,DEPT MOLEC ONCOL & VIROL,NUTLEY,NJ 07110
[4] ROCHE INST MOLEC BIOL,ROCHE RES CTR,DEPT NEUROSCI,NUTLEY,NJ 07110
关键词
Afterdischarge; c‐fos mRNA; Early gene; Hippocampus; Kindling; Seizure;
D O I
10.1111/j.1471-4159.1990.tb04595.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Abstract: Periodic induction of focal electrical seizure [afterdischarge (AD)] is an absolute prerequisite for the development of kindling, an animal model of complex partial epilepsy. Once established, it is a permanent condition. The mechanism(s) that translate ADs, which last tens of seconds, into life‐long alterations in the CNS is unclear. Cellular immediate‐early genes have been implicated in the conversion of short‐term stimuli to long‐term alterations in cellular phe‐notypes by regulating target gene expression. We have investigated the contribution of one such early gene, c‐fos, to this process. The relationship between ADs and expression of c‐fos gene in the rat hippocampus, a key structure in kindling development, was studied by analysis of mRNA levels. The low constitutive expression of c‐fos mRNA in the hippocampus was not altered by kindling. There was an “all‐or‐none” relationship between induction of c‐fos and the duration of AD. The threshold for induction was approximately 30 s of AD. Above‐threshold ADs induced c‐fos in both naive and kindled animals to the same extent and with identical temporal profiles. Although the expression of c‐fos is unchanged with kindling, c‐fos may nonetheless contribute to many long‐term changes of kindling, both adaptive and epileptogenic. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:1050 / 1055
页数:6
相关论文
共 18 条
[1]   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
[2]   FOS AND JUN - THE AP-1 CONNECTION [J].
CURRAN, T ;
FRANZA, BR .
CELL, 1988, 55 (03) :395-397
[3]  
Curran T, 1988, ONCOGENE HDB, P307
[4]   PARALLEL ASSOCIATION OF FOS AND JUN LEUCINE ZIPPERS JUXTAPOSES DNA-BINDING DOMAINS [J].
GENTZ, R ;
RAUSCHER, FJ ;
ABATE, C ;
CURRAN, T .
SCIENCE, 1989, 243 (4899) :1695-1699
[5]   A PERMANENT CHANGE IN BRAIN FUNCTION RESULTING FROM DAILY ELECTRICAL STIMULATION [J].
GODDARD, GV ;
MCINTYRE, DC ;
LEECH, CK .
EXPERIMENTAL NEUROLOGY, 1969, 25 (03) :295-&
[6]   EFFECT OF INHIBITORS OF PROTEIN-SYNTHESIS ON THE DEVELOPMENT OF KINDLED SEIZURES IN RATS [J].
JONEC, V ;
WASTERLAIN, CG .
EXPERIMENTAL NEUROLOGY, 1979, 66 (03) :524-532
[7]  
LABINER D M, 1989, Society for Neuroscience Abstracts, V15, P841
[8]  
MCNAMARA JO, 1987, NEUROTRANSMITTERS EP, P115
[9]  
MILLER AD, 1984, CELL, V36, P51
[10]   ROLE OF ION FLUX IN THE CONTROL OF C-FOS EXPRESSION [J].
MORGAN, JI ;
CURRAN, T .
NATURE, 1986, 322 (6079) :552-555