INTERACTION OF MK-801 WITH THE NICOTINIC ACETYLCHOLINE RECEPTOR-ASSOCIATED ION CHANNEL FROM ELECTROPLAX

被引：19

作者：

KAVANAUGH, MP ^{[1
]}

TESTER, BAC ^{[1
]}

WEBER, E ^{[1
]}

机构：

[1] OREGON HLTH SCI UNIV,VOLLUM INST ADV BIOMED RES,PORTLAND,OR 97201

来源：

EUROPEAN JOURNAL OF PHARMACOLOGY | 1989年 / 164卷 / 02期

关键词：

D O I：

10.1016/0014-2999(89)90487-1

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

收藏

页码：397 / 398

页数：2

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[2] THE DISSOCIATIVE ANESTHETICS, KETAMINE AND PHENCYCLIDINE, SELECTIVELY REDUCE EXCITATION OF CENTRAL MAMMALIAN NEURONS BY N-METHYL-ASPARTATE
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[3] [PHENCYCLIDINE-H-3 - A PROBE FOR THE IONIC CHANNEL OF THE NICOTINIC RECEPTOR
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[4] BLOCK OF N-METHYL-D-ASPARTATE-ACTIVATED CURRENT BY THE ANTICONVULSANT MK-801 - SELECTIVE BINDING TO OPEN CHANNELS
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[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (04) : 1307 - 1311
[5] THE ANTICONVULSANT MK-801 IS A POTENT N-METHYL-D-ASPARTATE ANTAGONIST
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