REDUCTION OF INVIVO BINDING OF [H-3] PAROXETINE IN MOUSE-BRAIN BY 3,4-METHYLENEDIOXYMETHAMPHETAMINE

被引:14
|
作者
HASHIMOTO, K
GOROMARU, T
机构
[1] Department of Radiopharmaceutical Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences, University of Fukuyama, Fukuyama, 729-02
关键词
3; 4-methylenedioxymethamphetamine; 5-hydroxytryptamine uptake sites; in vivo binding; mouse brain; [!sup]3[!/sup]H]paroxetine;
D O I
10.1016/0028-3908(90)90024-L
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of 3,4-methylenedioxymethamphetamine (MDMA) on the in vivo binding of [3H]paroxetine, a potent and selective 5-hydroxytryptamine (5-HT; serotonin) uptake inhibitor, in the brain of the mouse were studied. The distribution of radioactivity in the brain of the mouse, after intravenous administration of [3H]paroxetine, was significantly altered by pretreatment with MDMA (15mg/kg, i.p., 3hr before). The hypothalamus/cerebellum and cerebral cortex/cerebellum ratios, as a function of time, were significantly decreased after the pretreatment with MDMA, indicating that the in vivo binding of [3H]paroxetine to uptake sites for 5-HT in the brain of the mouse was significantly decreased by MDMA. These ratios could reflect those of the total binding, to the non-specific binding and free ligand, since the cerebellum has very low levels of binding for [3H]paroxetine. Furthermore, these ratios decreased after pretreatment with MDMA, in a dose-dependent manner. However, the binding of [3H]paroxetine to membranes from the brain of the mouse in vitro was not altered by treatment with MDMA. The discrepancy between thein vivo binding and in vitro binding of [3H]paroxetine in the brain of the mouse is discussed. © 1990.
引用
收藏
页码:633 / 639
页数:7
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