Effects of acute and chronic administration of MK-801 on c-Fos protein expression in mice brain regions implicated in schizophrenia and antagonistic action of clozapine

被引:1
|
作者
ZUO DaiyingCAO YueZHANG LanWANG HaifengWU YingliangDepartment of PharmacologyShenyang Pharmaceutical UniversityShenyang ChinaLiaoning Institute for Drug ControlShenyang China [1 ,2 ,1 ,1 ,1 ,1 ,110016 ,2 ,110023 ]
机构
关键词
c-Fos protein; clozapine; MK-801; schizophrenia;
D O I
10.14066/j.cnki.cn21-1349/r.2008.s1.111
中图分类号
R749.3 [精神分裂症]; R96 [药理学];
学科分类号
100602 ; 100706 ;
摘要
Objective To investigate the effects of acute and chronic administration of the non-competitive NMDA receptor antagonists MK-801 on c-Fos protein expression in different brain regions of mice and an-tagonistic action of clozapine.Methods Immunohistochemistry was used to detect the expression of c-Fos protein.Results MK-801(0.6 mg·kg-1)acute administration produced a significant increase in the expression of c-Fos protein in the layers Ⅲ-Ⅳ of posterior cingulate and retrosplenial(PC/RS)cortex,which was consistent with the previous reports.Moreover,we presented a new finding that MK-801(0.6 mg·kg-1)chronic administration for 8 days produced a significant increase of c-Fos protein expression in the PC/RS cortex,prefrontal cortex(PFC)and hypothalamus of mice.Among that,c-Fos protein expression in the PC/RS cortex of mice was most significant.Compared acute administration with chronic administration,we found that MK-801 chronic administration significantly increased the expression of c-Fos protein in the PC/RS cortex,PFC and hypothalamus.Furthermore,pretreatment of mice with clozapine significantly decreased the expression of c-Fos protein induced by MK-801 acute and chronic administration.Conclusions Marked expression of c-Fos protein induced by MK-801 is associated with neurotransmitters' change noted in our previous studies,and c-Fos protein,the marker of neuronal activation,might play an important role in the chronic pathophysiological process of schizophrenic model induced by NMDA receptor antagonist.
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页码:55 / 56
页数:2
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