Chongmyungtang attenuates kainic acid-induced seizure and mortal effect in the mouse

被引:10
作者
Jang, KJ
Lee, KH
Kim, SL
Choi, DY
Park, BK
Im, DH
Cho, YJ
Jhoo, WK
Kim, HC
机构
[1] KANGWEON NATL UNIV,COLL PHARM,CHUNCHON 200701,SOUTH KOREA
[2] BORYUNG PHARMACEUT CENT RES INST,KUNPO 435050,SOUTH KOREA
关键词
chongmyungtang; neuroprotective effect; kainic acid-induced neurotoxicity;
D O I
10.1007/BF02976204
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The Chongmyungtang (CMT; the combination of Acorus gramineus, polygala tenuifolia and Poria cocos) has been recognized to possess the preventive effect against several neurologic disorders in human. In this study, we examined the effect of CMT on the three parameters associated with kainic acid (KA)-induced neurotoxicities; seizure/mortality, increased fos-related antigen (FRA) and glial fibrillary acidic protein (GFAP) expression. KA induced vigorous convulsions lasting 4-6 hr. Pretreatments with CMT before KA injection significantly reduced the seizure intensity as well as the mortality. CMT pretreatments also attenuated the KA-induced increase in FRA/GFAP expression in the hippocampus. These results suggest that CMT has a neuroprotective effect against KA-induced neurotoxicities.
引用
收藏
页码:375 / 378
页数:4
相关论文
共 16 条
[1]   Long-term expression of the 35,000 mol wt fos-related antigen in rat brain after kainic acid treatment [J].
Bing, G ;
McMillian, M ;
Kim, H ;
Pennypacker, K ;
Feng, Z ;
Qi, Q ;
Kong, LY ;
Iadarola, M ;
Hong, JS .
NEUROSCIENCE, 1996, 73 (04) :1159-1174
[2]   SPATIAL MEMORY DEFICITS, INCREASED PHOSPHORYLATION OF THE TRANSCRIPTION FACTOR CREB, AND INDUCTION OF THE AP-1 COMPLEX FOLLOWING EXPERIMENTAL BRAIN INJURY [J].
DASH, PK ;
MOORE, AN ;
DIXON, CE .
JOURNAL OF NEUROSCIENCE, 1995, 15 (03) :2030-2039
[3]  
GREENAMYRE JT, 1985, J PHARMACOL EXP THER, V233, P254
[4]  
HUH I, 1994, DONGEUYBOKAM
[5]   MOLECULAR-BIOLOGY OF VERTEBRATE LEARNING - IS C-FOS A NEW BEGINNING [J].
KACZMAREK, L .
JOURNAL OF NEUROSCIENCE RESEARCH, 1993, 34 (04) :377-381
[6]   Dextromethorphan blocks opioid peptide gene expression in the rat hippocampus induced by kainic acid [J].
Kim, HC ;
Suh, HW ;
Bronstein, D ;
Bing, G ;
Wilson, B ;
Hong, JS .
NEUROPEPTIDES, 1997, 31 (02) :105-112
[7]  
Kim HC, 1996, NEUROTOXICOLOGY, V17, P375
[8]  
LEE CR, 1994, DRUGS AGING, V3, P257
[10]   PROTOONCOGENE TRANSCRIPTION FACTORS AND EPILEPSY [J].
MORGAN, JI ;
CURRAN, T .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1991, 12 (09) :343-349