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
相关论文
共 84 条
[1]   Safety and Efficacy of Repeated-Dose Intravenous Ketamine for Treatment-Resistant Depression [J].
aan het Rot, Marije ;
Collins, Katherine A. ;
Murrough, James W. ;
Perez, Andrew M. ;
Reich, David L. ;
Charney, Dennis S. ;
Mathew, Sanjay J. .
BIOLOGICAL PSYCHIATRY, 2010, 67 (02) :139-145
[2]   Calcium signals control wnt-dependent dendrite growth [J].
Alvania, Rebecca S. ;
Chen, Xi ;
Ginty, David D. .
NEURON, 2006, 50 (06) :813-815
[3]   NMDA receptor blockade at rest triggers rapid behavioural antidepressant responses [J].
Autry, Anita E. ;
Adachi, Megunai ;
Nosyreva, Elena ;
Na, Elisa S. ;
Los, Maarten F. ;
Cheng, Peng-fei ;
Kavalali, Ege T. ;
Monteggia, Lisa M. .
NATURE, 2011, 475 (7354) :91-U109
[4]   Chronic unpredictable stress promotes neuronal apoptosis in the cerebral cortex [J].
Bachis, Alessia ;
Cruz, Maria Idalia ;
Nosheny, Rachel L. ;
Mocchetti, Italo .
NEUROSCIENCE LETTERS, 2008, 442 (02) :104-108
[5]   Mood stabilizers target cellular plasticity and resilience cascades - Implications for the development of novel therapeutics [J].
Bachmann, RF ;
Schloesser, RJ ;
Gould, TD ;
Manji, HK .
MOLECULAR NEUROBIOLOGY, 2005, 32 (02) :173-202
[6]   Glial pathology in an animal model of depression: reversal of stress-induced cellular, metabolic and behavioral deficits by the glutamate-modulating drug riluzole [J].
Banasr, M. ;
Chowdhury, G. M. I. ;
Terwilliger, R. ;
Newton, S. S. ;
Duman, R. S. ;
Behar, K. L. ;
Sanacora, G. .
MOLECULAR PSYCHIATRY, 2010, 15 (05) :501-511
[7]   Glial Loss in the Prefrontal Cortex Is Sufficient to Induce Depressive-like Behaviors [J].
Banasr, Mounira ;
Duman, Ronald S. .
BIOLOGICAL PSYCHIATRY, 2008, 64 (10) :863-870
[8]  
Banasr Mounira, 2007, CNS & Neurological Disorders-Drug Targets, V6, P311, DOI 10.2174/187152707783220929
[9]   Antidepressant effects of ketamine in depressed patients [J].
Berman, RM ;
Cappiello, A ;
Anand, A ;
Oren, DA ;
Heninger, GR ;
Charney, DS ;
Krystal, JH .
BIOLOGICAL PSYCHIATRY, 2000, 47 (04) :351-354
[10]   Antidepressants increase neural progenitor cells in the human hippocampus [J].
Boldrini, Maura ;
Underwood, Mark D. ;
Hen, Rene ;
Rosoklija, Gorazd B. ;
Dwork, Andrew J. ;
Mann, J. John ;
Arango, Victoria .
NEUROPSYCHOPHARMACOLOGY, 2009, 34 (11) :2376-2389