Inhibition of excitotoxic neuronal death by methanol extract of Acori graminei rhizoma in cultured rat cortical neurons

被引:48
作者
Cho, JS [1 ]
Joo, NE
Kong, JY
Jeong, DY
Lee, KD
Kang, BS
机构
[1] Dongguk Univ, Coll Med, Dept Pharmacol, Kyongju 780714, South Korea
[2] Korea Res Inst Chem Technol, Screening Div, Taejon 305606, South Korea
[3] Dongguk Univ, Coll Nat Sci, Dept Chem, Kyongju 780714, South Korea
[4] Dongguk Univ, Coll Oriental Med, Dept Herbol, Kyongju 780714, South Korea
关键词
Acorus gramineus; neuroprotection; excitotoxicity; NMDA receptor; radioligand binding assays;
D O I
10.1016/S0378-8741(00)00262-2
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Acori graminei rhizoma (AGR) are reported to exhibit a number of pharmacological actions in the central nervous system. The effects of the methanol extract of AGR on excitotoxic neuronal death were evaluated in the present study using cultured rat cortical neurons. Based on the phase-contrast microscopic examinations of cultures and lactate dehydrogenase activities measured in the culture media, the glutamate-induced excitotoxicity was significantly inhibited by the extract. The inhibitory action of the extract was more potent and selective for the N-methyl-D-aspartate (NMDA) receptor-mediated toxicity. The AGR extract competed with [H-3]MDL 105,519 for the specific binding to the glycine site of the NMDA receptor with the IC50 value of 164.7 mug/ml. Modulation of the NMDA receptor activity by the extract was determined using [H-3]MK-801 binding studies. The reduction of the binding in the presence of the extract indicated the receptor inactivation by AGR. These results demonstrated that the methanol extract of AGR exhibited protective action against excitotoxic neuronal death, and that the neuroprotective action was primarily due to the blockade of NMDA receptor function by the interaction with the glycine binding site of the receptor. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:31 / 37
页数:7
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