Cytokine-serotonin interaction through IDO: a neurodegeneration hypothesis of depression

被引:292
作者
Myint, AM
Kim, YK
机构
[1] Univ Maastricht, Maastricht, Netherlands
[2] Korea Univ, Coll Med, Seoul 136701, South Korea
关键词
NECROSIS-FACTOR-ALPHA; INDOLEAMINE 2,3-DIOXYGENASE ACTIVITY; HUMAN MONONUCLEAR PHAGOCYTES; CENTRAL-NERVOUS-SYSTEM; MAJOR DEPRESSION; QUINOLINIC ACID; TRYPTOPHAN 2,3-DIOXYGENASE; PSYCHOLOGICAL STRESS; RECEPTOR ANTAGONIST; KYNURENINE PATHWAY;
D O I
10.1016/S0306-9877(03)00207-X
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
There are different theories and hypotheses related to the aetiology of depression. The interaction between brain 5-HT level and the activity of its autoreceptors plays a role in mood changes and depression. In major depression, activation of the inflammatory response system (IRS) and, increased concentrations of proinflammatory cytokines, prostaglandin E2 and negative immuno-regulatory cytokines in peripheral blood have been reported. Recently, pro-inflammatory cytokines have been found to have profound effects on the metabolism of brain serotonin through the enzyme indoleamine-2,3-dioxygenase (IDO) that metabolizes the tryptophan, the precursor of 5-HT to neurodegenerative quinolinate and neuroprotective kynurenate. The cytokine-serotonin interaction that leads to the challenge between quinolinate and kynurenate in the brain explains the neurodegeneration hypothesis of depression. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:519 / 525
页数:7
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