An affinity-modulating site on neuronal monoamine transport proteins

被引:39
作者
Plenge, P
Mellerup, ET
机构
[1] Laboratory of Neuropsychiatry, Department of Pharmacology, University of Copenhagen, DK-2100 Copenhagen Ø
来源
PHARMACOLOGY & TOXICOLOGY | 1997年 / 80卷 / 04期
关键词
D O I
10.1111/j.1600-0773.1997.tb00396.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The dissociation rates of [H-3]nisoxetine, [H-3]GBR 12935 and [H-3]citalopram from, respectively, the rat brain noradrenaline, dopamine and 5-HT transporters were found to be markedly affected by several drugs. Sertraline strongly attenuated the rate of dissociation of [H-3]nisoxetine from the noradrenaline transporter, while citaropram strongly attenuated that of [H-3]citalopram from the 5-HT transporter. The effects of both drugs were stereospecific. Less potent affinity-modulating drugs were identified with regards to [H-3]GBR 12935 dissociation from the dopamine transporter. All three neuronal monoamine transporters may thus have specific affinity-modulating sites which change the function of the transporters with possible implications for the reuptake of monoamines released during synaptic activity.
引用
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页码:197 / 201
页数:5
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