Oscillatory Serotonin Function in Depression

被引:32
作者
Salomon, Ronald M. [1 ]
Cowan, Ronald L. [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Psychiat, Nashville, TN 37212 USA
[2] Vanderbilt Univ, Sch Med, Dept Radiol, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Nashville, TN 37212 USA
基金
美国国家卫生研究院;
关键词
chronobiology; depression; serotonin; dopamine; tryptophan depletion; raphe nucle; MDMA; fMRI; DORSAL RAPHE NUCLEUS; LOW-FREQUENCY OSCILLATIONS; TOTAL PLASMA TRYPTOPHAN; MESSENGER-RNA EXPRESSION; VENTRAL TEGMENTAL AREA; TIME-SERIES ANALYSIS; HUMAN BRAIN-STEM; SUPRACHIASMATIC NUCLEUS; MONOAMINE METABOLITES; BIOLOGICAL RHYTHMS;
D O I
10.1002/syn.21675
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Oscillations in brain activities with periods of minutes to hours may be critical for normal mood behaviors. Ultradian (faster than circadian) rhythms of mood behaviors and associated central nervous system activities are altered in depression. Recent data suggest that ultradian rhythms in serotonin (5HT) function also change in depression. In two separate studies, 5HT metabolites in cerebrospinal fluid (CSF) were measured every 10 min for 24 h before and after chronic antidepressant treatment. Antidepressant treatments were associated with enhanced ultradian amplitudes of CSF metabolite levels. Another study used resting-state functional magnetic resonance imaging (fMRI) to measure amplitudes of dorsal raphe activation cycles following sham or active dietary depletions of the 5HT precursor (tryptophan). During depletion, amplitudes of dorsal raphe activation cycles increased with rapid 6 s periods (about 0.18 Hz) while functional connectivity weakened between dorsal raphe and thalamus at slower periods of 20 s (0.05 Hz). A third approach studied MDMA (ecstasy, 3,4-methylenedioxy-N-methylamphetamine) users because of their chronically diminished 5HT function compared with non-MDMA polysubstance users (Karageorgiou et al., 2009). Compared with a non-MDMA using cohort, MDMA users showed diminished fMRI intra-regional coherence in motor regions along with altered functional connectivity, again suggesting effects of altered 5HT oscillatory function. These data support a hypothesis that qualities of ultradian oscillations in 5HT function may critically influence moods and behaviors. Dysfunctional 5HT rhythms in depression may be a common endpoint and biomarker for depression, linking dysfunction of slow brain network oscillators to 5HT mechanisms affected by commonly available treatments. 5HT oscillatory dysfunction may define illness subtypes and predict responses to serotonergic agents. Further studies of 5HT oscillations in depression are indicated. Synapse 67:801-820, 2013. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:801 / 820
页数:20
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