INHIBITION AND DISSOCIATION OF [H-3] PAROXETINE BINDING TO HUMAN PLATELETS

被引：10

作者：

ANDERSSON, A ^{[1
]}

MARCUSSON, J ^{[1
]}

机构：

[1] UMEA UNIV,DEPT GERIATR MED,S-90187 UMEA,SWEDEN

来源：

NEUROPSYCHOBIOLOGY | 1989年 / 22卷 / 03期

关键词：

D O I：

10.1159/000118607

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

引用

页码：135 / 140

页数：6

共 16 条

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[2]

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[3] DIFFERENCES BETWEEN SODIUM-DEPENDENT AND DESIPRAMINE-DEFINED [H-3]IMIPRAMINE BINDING IN INTACT HUMAN-PLATELETS [J].

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BIOLOGICAL PSYCHIATRY, 1989, 25 (05) :576-584

[4]

HUMPHREYS CJ, 1988, MOL PHARMACOL, V33, P657

[5] HUMAN-PLATELETS POSSESS MULTIPLE [H-3]IMIPRAMINE BINDING-SITES [J].

IENI, JR ;

ZUKIN, SR ;

VANPRAAG, HM .

EUROPEAN JOURNAL OF PHARMACOLOGY, 1984, 106 (03) :669-672

[6] EFFECTS OF ANTIDEPRESSANTS ON MONOAMINE TRANSPORTERS [J].

LANGER, SZ ;

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[7] STUDIES ON THE SEROTONIN TRANSPORTER IN PLATELETS [J].

LANGER, SZ ;

GALZIN, AM .

EXPERIENTIA, 1988, 44 (02) :127-130

[8] DISSOCIATION KINETICS OF [H-3] PAROXETINE BINDING TO RAT-BRAIN CONSISTENT WITH A SINGLE-SITE MODEL OF THE ANTIDEPRESSANT BINDING 5-HYDROXYTRYPTAMINE UPTAKE SITE [J].

MARCUSSON, J ;

ERIKSSON, K .

JOURNAL OF NEUROCHEMISTRY, 1988, 51 (05) :1477-1481

[9]

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[10]

MARCUSSON J, 1990, IN PRESS PSYCHOPHARM

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