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金刚烷胺通过抑制再摄取和拮抗N-甲基-D-天冬氨酸来提高纹状体细胞外多巴胺水平。

Amantadine increases the extracellular dopamine levels in the striatum by re-uptake inhibition and by N-methyl-D-aspartate antagonism.

作者信息

Mizoguchi K, Yokoo H, Yoshida M, Tanaka T, Tanaka M

机构信息

Department of Pharmacology, Kurume University School of Medicine, Japan.

出版信息

Brain Res. 1994 Oct 31;662(1-2):255-8. doi: 10.1016/0006-8993(94)90821-4.

Abstract

This study was performed to investigate the mechanism how amantadine increases the extracellular dopamine (DA) levels in the striatum in vivo. Local application of amantadine (1 mM, 40 min) to the striatum through the dialysis membrane significantly increased the extracellular DA levels. Coadministration of nomifensine (10 mM, 120 min), an inhibitor of neuronal DA uptake, into the perfusion fluid attenuated the amantadine-induced increase in DA outflow. The amantadine-induced increases in the extracellular DA levels were also inhibited by co-perfusion with Ringer containing high Mg2+ (15 mM, 120 min) or with MK-801 (1 microM, 80 min). These findings suggest that amantadine increases the extracellular DA levels in the striatum by inhibiting the re-uptake of DA and/or by blocking the channel in the N-methyl-D-aspartate (NMDA) receptor, which results in antagonism of NMDA receptor function.

摘要

本研究旨在探讨金刚烷胺在体内增加纹状体细胞外多巴胺(DA)水平的机制。通过透析膜向纹状体局部应用金刚烷胺(1 mM,40分钟)可显著增加细胞外DA水平。将神经元DA摄取抑制剂诺米芬辛(10 mM,120分钟)共同注入灌注液中,可减弱金刚烷胺诱导的DA流出增加。与含高镁离子(15 mM,120分钟)的林格液或MK-801(1 microM,80分钟)共同灌注也可抑制金刚烷胺诱导的细胞外DA水平升高。这些发现表明,金刚烷胺通过抑制DA的再摄取和/或阻断N-甲基-D-天冬氨酸(NMDA)受体中的通道来增加纹状体细胞外DA水平,这导致NMDA受体功能的拮抗作用。

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