SUPPRESSED EPILEPTOGENESIS IN BDNF MUTANT MICE

被引:221
作者
KOKAIA, M
ERNFORS, P
KOKAIA, Z
ELMER, E
JAENISCH, R
LINDVALL, O
机构
[1] MIT, NINE CAMBRIDGE CTR, WHITEHEAD INST BIOMED RES, CAMBRIDGE, MA 02142 USA
[2] MIT, DEPT BIOL, CAMBRIDGE, MA 02142 USA
[3] KAROLINSKA INST, DEPT MED BIOCHEM & BIOPHYS, MOLEC NEUROBIOL LAB, S-17177 STOCKHOLM, SWEDEN
关键词
D O I
10.1006/exnr.1995.1024
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Kindling is an animal model of epilepsy in which repeated electrical stimulations lead to progressive and permanent amplification of seizure activity, culminating in generalized convulsions. Each brief period of seizure activity during kindling epileptogenesis causes a marked, transient increase of the synthesis of brain-derived neurotrophic factor (BDNF) in cortical and hippocampal neurons. We find that the development of kindling is markedly suppressed in mice heterozygous for a deletion of the BDNF gene. In contrast, the maintenance of kindling is unaffected. The mutant mice show lower levels of BDNF mRNA in cortical and hippocampal neurons after seizures than do wild-type mice. Hippocampal messy fiber sprouting is augmented in BDNF mutants but there are no other morphological abnormalities. These results show that BDNF plays an important role in establishing hyperexcitability during epileptogenesis, probably by increasing efficacy in stimulated synapses. (C) 1995 Academic Press, Inc.
引用
收藏
页码:215 / 224
页数:10
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