Sex differences in striatal presynaptic dopamine synthesis capacity in healthy subjects

被引:159
作者
Laakso, A
Vilkman, H
Bergman, J
Haaparanta, M
Solin, O
Syvälahti, E
Salokangas, RKR
Hietala, J
机构
[1] Turku Univ, Cent Hosp, Turku PET Ctr, Turku 20520, Finland
[2] Turku Univ, Cent Hosp, Turku PET Ctr, Accelerator Lab, Turku 20520, Finland
[3] Turku Univ, Cent Hosp, Turku PET Ctr, Medic PET, Turku 20520, Finland
[4] Turku Univ, Cent Hosp, Dept Psychiat, Turku 20520, Finland
[5] Univ Turku, Turku PET Ctr, Turku, Finland
[6] Univ Turku, Dept Pharmacol & Clin Pharmacol, Turku, Finland
基金
芬兰科学院;
关键词
fluorodopa; striatum; caudate; putamen; positron emission tomography; sex;
D O I
10.1016/S0006-3223(02)01369-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: There are sex differences in the clinical features of several neuropsychiatric illnesses associated with dopamine dysfunction. The effects of sex on brain dopaininergic function have been sparsely studied in human subjects using modern imaging techniques. We have previously reported that the apparent affinity of [C-11]raclopride for striatal D-2 dopamine receptors in vivo is lower in women than in men, whereas D-2 receptor density is not different. This finding indirectly suggests that women have a higher synaptic concentration of dopamine in the striatum. We explored further the basis of this phenomenon in an independent study and hypothesized that striatal presynaptic dopamine synthesis capacity would also be elevated in women. Methods: A total of 23 healthy men and 12 healthy women (age range 20-60 years) were studied using positron emission tomography and [F-18]fluorodopa. Results: Women had significantly higher striatal [F-18]fluorodopa uptake (Ki values) than men. The difference was more marked in the caudate (+26%) than in the putamen (+ 12%). In addition, there was a negative correlation between striatal [F-18]fluorodopa Ki values and age in men but not in women. Conclusions: The results further substantiate sex differences in striatal dopaminergic function in humans. This finding may be associated with sex differences in vulnerability and clinical course of neuropsychiatric disorders with dopaminergic dysregulation, e.g., schizophrenia, alcohol dependence, and Parkinson's disease. (C) 2002 Society of Biological Psychiatry.
引用
收藏
页码:759 / 763
页数:5
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