Decreased striatal dopamine transporter binding in vivo in chronic schizophrenia

被引:79
|
作者
Laakso, A
Bergman, J
Haaparanta, M
Vilkman, H
Solin, O
Syvälahti, E
Hietala, J [1 ]
机构
[1] Turku PET Ctr, Accelerator Lab, Turku 20520, Finland
[2] Turku PET Ctr, Medicity PET, Turku 20520, Finland
[3] Univ Turku, Dept Pharmacol & Clin Pharmacol, FIN-20520 Turku, Finland
[4] Univ Turku, Dept Psychiat, FIN-20520 Turku, Finland
[5] Univ Turku, Cent Hosp, Turku PET Ctr, FIN-20520 Turku, Finland
基金
芬兰科学院;
关键词
CFT; dopamine transporter; positron emission tomography; schizophrenia; WIN 35,428;
D O I
10.1016/S0920-9964(00)00095-5
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
We have previously reported that average striatal dopamine transporter (DAT) binding in vivo is unaltered in neuroleptic-naive first-episode schizophrenic patients [Laakso et al., Am. J. Psychiatry 157 (2000) 269]. However, as it has been suggested that some of the brain changes in schizophrenia may vary depending on the illness phase, we studied DAT density in eight stable, medicated chronic schizophrenic patients and eight matched controls using positron emission tomography and [F-18]CFT, a marker of dopamine nerve terminals. [F-18]CFT binding potentials were significantly lower in chronic schizophrenic patients than in controls, both in the caudate and the putamen (-9 to -16%). Together with the finding of unchanged average striatal DAT levels in first-episode patients and relative insensitivity of striatal [F-18]CFT binding to endogenous dopamine and neuroleptic drugs, the result is in line with a relative loss of striatal dopaminergic nerve terminals and/or decreased expression of DAT in a subset of chronic schizophrenic patients. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:115 / 120
页数:6
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