The Effects of Acute Tryptophan Depletion on Brain Activation During Cognition and Emotional Processing in Healthy Volunteers

被引:28
|
作者
Evers, E. A. T. [1 ]
Sambeth, A. [1 ]
Ramaekers, J. G. [1 ]
Riedel, W. J. [1 ]
van der Veen, F. M. [2 ]
机构
[1] Maastricht Univ, Fac Psychol & Neurosci, Dept Neuropsychol & Psychopharmacol, Maastricht, Netherlands
[2] Erasmus MC, Dept Psychiat, Rotterdam, Netherlands
关键词
Serotonin; acute tryptophan depletion; cognition; emotion; fMRI; PET; EEG; MEG; SEROTONIN TRANSPORTER POLYMORPHISM; RESPONSE-INHIBITION; EXECUTIVE FUNCTIONS; PREFRONTAL CORTEX; EPISODIC MEMORY; 5-HYDROXYINDOLEACETIC ACID; ANTIDEPRESSANT TREATMENT; BEHAVIORAL-INHIBITION; INTENSITY DEPENDENCE; RECEPTOR ANTAGONIST;
D O I
10.2174/138161210791293060
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Acute tryptophan depletion (ATD), a method to temporarily lower central serotonin levels, has been used to study the functioning of the serotonergic system. Relatively recent studies that examined the effects of ATD on brain activation associated with cognitive and emotional processing in healthy volunteers are reviewed. An overview of the findings in healthy volunteers is important for the interpretation of the effect of ATD on brain activation in patients with an affective disorder, such as major depression. These studies show that during response control and negative feedback processing ATD modulates the BOLD response in the inferior/orbitofrontal cortex, the anterior cingulate cortex and the dorsomedial prefrontal cortex. During emotional processing, it is consistently found that ATD modulates the BOLD response in the amygdala. These brain regions also show abnormal activation in depressed patients. However, at the moment it remains unclear if the changes induced by ATD are related to decreased basal serotonin (5-HT) release or the result of other biochemical changes that are mediated by ATD. Future studies should implement methodological improvements, explore the possibilities of new promising imaging techniques and expand investigations into the effects of ATD on basal 5-HT release and other biochemical mechanisms that might be modulated by ATD.
引用
收藏
页码:1998 / 2011
页数:14
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