Dopamine transporter in vitro binding and in vivo imaging in the brain

被引:6
作者
Bergström, KA
Tupala, E
Tiihonen, J
机构
[1] Kuopio Univ Hosp, Dept Clin Physiol & Nucl Med, FIN-70210 Kuopio, Finland
[2] Univ Kuopio, Niuvanniemi Hosp, Dept Forens Psychiat, FIN-70240 Kuopio, Finland
来源
PHARMACOLOGY & TOXICOLOGY | 2001年 / 88卷 / 06期
关键词
D O I
10.1034/j.1600-0773.2001.880601.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Much research interest has lately been focused on the dopamine transporter function in brain. Recent findings indicate that dopamine reuptake is more like a highly regulated than a constitutive determinant of dopamine clearance. Positron emission tomography (PET) and single-photon emission tomography (SPET) offer unique methods to study dopamine transporter function. Results from in vivo PET and SPET studies correspond well with in vitro studies performed on post mortem human brain tissue. Considering some of the variances between in vitro and in vivo receptor binding phenomena it may be that the role of a compound to alter binding to monoamine uptake sites in vitro does not indicate its potential to affect monoamine transporters after administration in vivo. This discrepancy may be better understood taking into account recant studies indicating the possibility of a rapid regulation of transporter function and surface expression. Furthermore, the dopamine transporter is a fruitful target for CNS drug discovery Fundamental nature of drug actions in vivo may be studied using demonstrated in vitro and in vivo imaging methods.
引用
收藏
页码:287 / 293
页数:7
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