INCREASE IN GAP-43 AND GFAP IMMUNOREACTIVITY IN THE RAT HIPPOCAMPUS SUBSEQUENT TO PERFORANT PATH KINDLING

被引:30
作者
DALBY, NO [1 ]
RONDOUIN, G [1 ]
LERNERNATOLI, M [1 ]
机构
[1] INST BIOL,EXPTL MED LAB,CNRS,UPR 9008,INSERM,U249,MONTPELLIER,FRANCE
关键词
EPILEPSY; SEIZURE; TRANSMITTER RELEASE; NEURONAL PLASTICITY; ASTROCYTE;
D O I
10.1002/jnr.490410507
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 which is accompanied by morphological and biochemical changes in the brain, including sprouting of fibers and increased transmitter release, Here we have examined the immunocytochemical expression of 1) GAP-43, a growth-associated protein, which is a neuron-specific PKC substrate, particularly expressed in development and regeneration and 2) glial fibrillary acidic protein (GFAP), part of the astrocytic cytoskeleton, after perforant path kindling, Subsequent to kindling, GAP-43 immunoreactivity was increased in CA1 stratum lacunosum-moleculare and the inner and outer molecular layer of the fascia dentata. Other hippocampal subregions showed a lower increase. GFAP immunoreactivity was increased in the entire hippocampus, but especially in stratum lacunosum-moleculare of the CA1 and the hilus of fascia dentata. The difference between the number of GFAP-positive profiles in the hippocampus of control rats and in fully kindled rats was found to be non-significant. We interpret these findings as being related to both plastic neuronal changes and possible neuronal degeneration. (C) 1995 Wiley Liss, Inc.
引用
收藏
页码:613 / 619
页数:7
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