Cell atrophy and loss in depression: reversal by antidepressant treatment

被引:154
作者
Banasr, Mounira
Dwyer, Jason M.
Duman, Ronald S. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT 06508 USA
关键词
ADULT HIPPOCAMPAL NEUROGENESIS; BDNF VAL66MET POLYMORPHISM; D-ASPARTATE ANTAGONIST; STRESS-INDUCED CHANGES; PREFRONTAL CORTEX; UNPREDICTABLE STRESS; NEUROTROPHIC FACTORS; BEHAVIORAL ACTIONS; GABAERGIC NEURONS; RECEPTOR BLOCKADE;
D O I
10.1016/j.ceb.2011.09.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Depression is associated with structural alterations in limbic brain regions that control emotion and mood. Studies of chronic stress in animal models and postmortem tissue from depressed subjects demonstrate that these structural alterations result from atrophy and loss of neurons and glial cells. These findings indicate that depression and stress-related mood disorders can be considered mild neurodegenerative disorders. Importantly, there is evidence that these structural alterations can be blocked or even reversed by elimination of stress and by antidepressant treatments. A major focus of current investigations is to characterize the molecular signaling pathways and factors that underlie these effects of stress, depression, and antidepressant treatment. Recent advances in this research area are discussed and potential novel targets for antidepressant development are highlighted.
引用
收藏
页码:730 / 737
页数:8
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