COMPARISON OF THE EFFECTS OF MK-801 AND PHENCYCLIDINE ON CATECHOLAMINE UPTAKE AND NMDA-INDUCED NOREPINEPHRINE RELEASE

被引：137

作者：

SNELL, LD ^{[1
]}

YI, SJ ^{[1
]}

JOHNSON, KM ^{[1
]}

机构：

[1] UNIV TEXAS,MED BRANCH,DEPT PHARMACOL & TOXICOL,GALVESTON,TX 77550

来源：

EUROPEAN JOURNAL OF PHARMACOLOGY | 1988年 / 145卷 / 02期

关键词：

D O I：

10.1016/0014-2999(88)90235-X

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：223 / 226

页数：4

共 10 条

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CLINESCHMIDT, BV
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[2] ANTICONVULSANT ACTIVITY OF (+)-5-METHYL-10, 11-DIHYDRO-5H-DIBENZO[A,D]CYCLOHEPTEN-5, 10-IMINE (MK-801), A SUBSTANCE WITH POTENT ANTICONVULSANT, CENTRAL SYMPATHOMIMETIC, AND APPARENT ANXIOLYTIC PROPERTIES
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BUNTING, PR
[J]. DRUG DEVELOPMENT RESEARCH, 1982, 2 (02) : 123 - 134
[3] EFFECTS OF PHENCYCLIDINE ON UPTAKE OF CATECHOLAMINE-H-3 BY RAT STRIATAL AND HYPOTHALAMIC SYNAPTOSOMES
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[J]. LIFE SCIENCES, 1976, 18 (10) : 1105 - 1110
[4] EFFECTS OF PHENCYCLIDINE (PCP)-LIKE DRUGS ON TURNING BEHAVIOR, H-3-DOPAMINE UPTAKE, AND PCP-H-3 BINDING
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SNELL, LD
[J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1985, 22 (05) : 731 - 735
[5] JONES SM, 1987, J PHARMACOL EXP THER, V240, P492
[6] THE NOVEL ANTICONVULSANT MK-801 INTERACTS WITH CENTRAL PHENCYCLIDINE RECOGNITION SITES IN RAT-BRAIN
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[J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1987, 135 (02) : 261 - 263
[7] POSSIBLE THERAPEUTIC APPLICATIONS OF ANTAGONISTS OF EXCITATORY AMINO-ACID NEUROTRANSMITTERS
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[J]. CLINICAL SCIENCE, 1985, 68 (02) : 113 - 122
[8] SNELL LD, 1986, J PHARMACOL EXP THER, V238, P938
[9] [TCP-H-3 - A NEW TOOL WITH HIGH-AFFINITY FOR THE PCP RECEPTOR IN RAT-BRAIN
VIGNON, J
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[J]. BRAIN RESEARCH, 1983, 280 (01) : 194 - 197
[10] THE ANTICONVULSANT MK-801 IS A POTENT N-METHYL-D-ASPARTATE ANTAGONIST
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IVERSEN, LL
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (18) : 7104 - 7108

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