5-HT and depression: is the glass half-full?

被引:98
作者
Sharp, Trevor [1 ]
Cowen, Philip J. [2 ]
机构
[1] Univ Oxford, Dept Pharmacol, Oxford OX1 3QT, England
[2] Univ Oxford, Warneford Hosp, Dept Psychiat, Oxford OX3 7JX, England
基金
英国医学研究理事会;
关键词
SEROTONIN TRANSPORTER GENE; POSITRON-EMISSION; RECEPTOR-BINDING; SELECTIVE SEROTONIN; REUPTAKE INHIBITORS; HEALTHY-VOLUNTEERS; STRESS; MODEL; MOOD; ANTIDEPRESSANTS;
D O I
10.1016/j.coph.2011.02.003
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Mood disorders such as major depression are common illnesses with considerable morbidity and significant mortality. A long-standing theory is that a breakdown in brain serotonin (5-hydroxytryptamine; 5-HT) signalling is critically involved in the symptoms and drug treatment of clinical depression. However, the nature of this 5-HT defect has proved to be frustratingly elusive, and it remains unclear how the 5-HT signalling effects of antidepressant drugs might alter neuropsychological mechanisms to bring about relief of depressed mood. This article highlights recent discoveries that advance our understanding of how 5-HT-evoked changes at molecular, cellular and neuropsychological levels might interact to alleviate the symptoms of clinical depression.
引用
收藏
页码:45 / 51
页数:7
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