Dextromethorphan modulates the AP-1 DNA-binding activity induced by kainic acid

被引:35
|
作者
Kim, HC [1 ]
Bing, GY
Jhoo, WK
Ko, KH
Kim, WK
Lee, DC
Shin, EJ
Hong, JS
机构
[1] Kangweon Natl Univ, Korea Inst Drug Abuse, Coll Pharm, Dept Pharm,Sect Pharmacol & Toxicol, Chunchon 200701, South Korea
[2] Oklahoma Med Res Fdn, Free Radical Biol & Aging Res Program, Oklahoma City, OK 73104 USA
[3] Seoul Natl Univ, Coll Pharm, Ctr Biofunct Mol, Seoul 151742, South Korea
[4] Ewha Womans Univ, Ewha Med Res Ctr, Coll Med, Dept Pharmacol, Seoul 151056, South Korea
[5] NIEHS, Lab Pharmacol & Chem, NIH, Res Triangle Pk, NC 27709 USA
关键词
dextromethorphan; neuroprotection; hippocampus; kainic acid; activator protein-1; Fos-related antigen;
D O I
10.1016/S0006-8993(99)01155-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have recently reported that dextromethorphan attenuates the neurotoxicity induced by kainic acid in a dose-related fashion. Pretreatments with dextromethorphan (50 mg/kg, p.o. x2) significantly reduced the activator protein-1 DNA-binding activity and the Fos-related antigen-immunoreactive protein induced by kainic acid (10 mg/kg, i.p.) in the CA1, but not the CA3 or the dentate gyrus sector of the rat hippocampus. Paradoxically, dextromethorphan itself caused an elevated activator protein-1 DNA-binding activity and Fos-related antigen-immunoreactive protein in the CA1 region which lasted for at least 4 days. The results suggest that the CA1 area is the critical site for mediating the putative neuroprotective effect induced by dextromethorphan. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:125 / 132
页数:8
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