Effects of tryptophan depletion on the serotonin transporter in healthy humans

被引:70
作者
Praschak-Rieder, N
Wilson, AA
Hussey, D
Carella, A
Wei, C
Ginovart, N
Schwarz, MJ
Zach, J
Houle, S
Meyer, JH
机构
[1] Univ Toronto, Vivian M Rakoff PET Imaging Ctr, Ctr Addict & Mental Hlth, Toronto, ON M5T 1R8, Canada
[2] Univ Toronto, Dept Psychiat, Toronto, ON M5T 1R8, Canada
[3] Univ Vienna, Dept Gen Psychiat, A-1010 Vienna, Austria
[4] Univ Munich, Dept Psychiat, D-80539 Munich, Germany
基金
奥地利科学基金会;
关键词
tryptophan depletion; serotonin transporter; healthy subjects; positron emission tomography; C-11]DASB;
D O I
10.1016/j.biopsych.2005.04.038
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Lowering of brain serotonin by acute tryptophan depletion (TD) frequently leads to transient symptoms of depression in vulnerable individuals but not in euthymic health subjects with a negative family history of depression. The effects of TD on regional serotonin transporter binding potential (5-HTT BP), an index of 5-HTT density and affinity, were studied in healthy individuals using 3-(11)C-amino-4-(2-dimenthylaminomethylphenylsulfanyl)benzonitrile ([C-11]DASB) positron emission tomography (PET). Adaptive decreased in 5-HTT density and/or affinity during TD would be a possible compensatory mechanism to maintain sufficient extracellular serotonin levels during TD, thereby preventing a depressive relapse. Methods: Regional noninvasive 5-HTT BP was found in 25 healthy subjects using [C-11]DASB PET. Fourteen subjects were scanned twice, once after TD and once after sham depletion, and 11 other healthy subjects were scanned twice to measure test-retest reliability of the method. Results: None of the healthy subjects experienced depressive symptoms during TD and there was no difference in regional 5-HTT BP during TD as compared with sham depletion. Conclusions: Acute changes in 5-HTT density or affinity are unlikely to play a role in protecting healthy subjects against mood symptoms during TD. Other mechanisms that may be associated with greater resilience against acute lowering of extracellular serotonin should be explored to gain further into the neurochemical basis of different vulnerabilities to short-term depressive relapse.
引用
收藏
页码:825 / 830
页数:6
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