The mesolimbic dopamine reward circuit in depression

被引:1570
作者
Nestler, Eric J.
Carlezon, William A., Jr.
机构
[1] Texas A&I Univ, SW Med Ctr, Dept Psychiat, Dallas, TX 75390 USA
[2] Texas A&I Univ, SW Med Ctr, Ctr Basic Neurosci, Dallas, TX 75390 USA
[3] Harvard Univ, Sch Med, Dept Psychiat, Belmont, MA 02178 USA
[4] McLean Hosp, Belmont, MA 02178 USA
关键词
ventral striatum; nucleus accumbens; ventral tegmental area; CREB; dynorphin; BDNF; MCH; orexin; melanocortin; Clock; NPAS2;
D O I
10.1016/j.biopsych.2005.09.018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The neural circuitry that mediates mood under normal and abnormal conditions remains incompletely understood. Most attention in the field has focused on hippocampal and frontal cortical regions for their role in depression and antidepressant action. While these regions no doubt play important roles in these phenomena, there is compelling evidence that other brain regions are also involved. Here we focus on the potential role of the nucleus accumbens (NAc; ventral striatum) and its dopaminergic input from the ventral tegmental area (VTA), which form the mesolimbic dopamine system, in depression. The mesolimbic dopamine system is most often associated with the rewarding effects of food, sex, and drugs of abuse. Given the prominence of anhedonia, reduced motivation, and decreased energy level in most individuals with depression, we propose that the NAc and VTA contribute importantly to the pathophysiology and symptomatology of depression and may even be involved in its etiology. We review recent studies showing that manipulations of key proteins (e.g. CREB, dynorphin, BDNF, MCH, or Clock) within the VTA-NAc circuit of rodents produce unique behavioral phenotypes, some of which are directly relevant to depression. Studies of these and other proteins in the mesolimbic dopamine system have established novel approaches to modeling key symptoms of depression in animals, and could enable the development of antidepressant medications with fundamentally new mechanisms of action.
引用
收藏
页码:1151 / 1159
页数:9
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