首页 | 本学科首页   官方微博 | 高级检索  
     

石杉碱甲对大鼠大脑皮层NMDA受体的调制作用
引用本文:王晓东 胡国渊. 石杉碱甲对大鼠大脑皮层NMDA受体的调制作用[J]. 中国药理学报, 1999, 20(1): 31-35
作者姓名:王晓东 胡国渊
摘    要:


关 键 词:石杉碱甲 胆碱酯酶抑制剂 NMDA受体 大脑皮质

Modulation of NMDA receptor by huperzine A in rat cerebral cortex.
X D Wang,J M Zhang,H H Yang,G Y Hu. Modulation of NMDA receptor by huperzine A in rat cerebral cortex.[J]. Acta Pharmacologica Sinica, 1999, 20(1): 31-35
Authors:X D Wang  J M Zhang  H H Yang  G Y Hu
Affiliation:State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, China.
Abstract:
AIM: To investigate the effects of huperzine A (Hup A) on NMDA receptors in rat cerebral cortex. METHODS: 1) The effect of hup A on NMDA-induced current was studied in acutely dissociated rat hippocampal pyramidal neurons using whole-cell recording. 2) The effect of Hup A on NMDA receptor binding was assessed using [3H] dizocilpine (Diz) binding assay in synaptic membrane preparation of rat cerebral cortex. RESULTS: 1) Hup A reversibly inhibited NMDA-induced current in a concentration-dependent manner with IC50 of 45.4 mumol.L-1. 2) Hup A inhibited the specific binding of [3H]MK-801 to extensively washed synaptic membrane of rat cerebral cortex in a concentration-dependent manner with IC50 of 0.5 (0.1-1.9) mumol.L-1 (n = 4). 3) L-Glutamate 10 mumol.L-1 markedly increased [3H] MK-801 binding. In the presence of L-glutamate, Hup A 0.001-0.1 mumol.L-1 caused a further increase of the binding, whereas Hup A 1-300 mumol.L-1 inhibited the binding in a concentration-dependent manner with IC50 of 12.3 (5.8-26.3) mumol.L-1 (n = 5). CONCLUSION: Hup A acted as an antagonist of NMDA receptor in cerebral cortex in addition to its inhibitory effect on acetylcholinesterase.
Keywords:
本文献已被 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号