Neuronal Network Plasticity and Recovery From Depression

被引:151
作者
Castren, Eero [1 ]
机构
[1] Univ Helsinki, Ctr Neurosci, FIN-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
OCULAR DOMINANCE PLASTICITY; LATE-LIFE DEPRESSION; NEUROTROPHIC FACTOR; VISUAL-CORTEX; EXPOSURE THERAPY; DRUG DISCOVERY; FOLLOW-UP; ANTIDEPRESSANT; BRAIN; MOOD;
D O I
10.1001/jamapsychiatry.2013.1
中图分类号
R749 [精神病学];
学科分类号
100204 [神经病学];
摘要
The brain processes sensory information in neuronal networks that are shaped by experience, particularly during early life, to optimally represent the internal and external milieu. Recent surprising findings have revealed that antidepressant drugs reactivate a window of juvenile-like plasticity in the adult cortex. When antidepressant-induced plasticity was combined with appropriate rehabilitation, it brought about a functional recovery of abnormally wired neuronal networks. These observations suggest that antidepressants act permissively to facilitate environmental influence on neuronal network reorganization and so provide a plausible neurobiological explanation for the enhanced effect of combining antidepressant treatment with psychotherapy. The results emphasize that pharmacological and psychological treatments of mood disorders are closely entwined: the effect of antidepressant-induced plasticity is facilitated by rehabilitation, such as psychotherapy, that guides the plastic networks, and psychotherapy benefits from the enhanced plasticity provided by the drug treatment. Optimized combinations of pharmacological and psychological treatments might help make best use of existing antidepressant drugs and reduce the number of treatment-resistant patients. The network hypothesis of antidepressant action presented here proposes that recovery from depression and related mood disorders is a gradual process that develops slowly and is facilitated by structured guidance and rehabilitation.
引用
收藏
页码:983 / 989
页数:7
相关论文
共 93 条
[1]
A double blind placebo RCT to investigate the effects of serotonergic modulation on brain excitability and motor recovery in stroke patients [J].
Acler, Michele ;
Robol, E. ;
Fiaschi, A. ;
Manganotti, P. .
JOURNAL OF NEUROLOGY, 2009, 256 (07) :1152-1158
[2]
Neurodevelopmental origins of depressive disorders [J].
Ansorge, Mark S. ;
Hen, Rene ;
Gingrich, Jay A. .
CURRENT OPINION IN PHARMACOLOGY, 2007, 7 (01) :8-17
[3]
Early-life blockade of the 5-HT transporter alters emotional behavior in adult mice [J].
Ansorge, MS ;
Zhou, MM ;
Lira, A ;
Hen, R ;
Gingrich, JA .
SCIENCE, 2004, 306 (5697) :879-881
[4]
Brain-Derived Neurotrophic Factor and Neuropsychiatric Disorders [J].
Autry, Anita E. ;
Monteggia, Lisa M. .
PHARMACOLOGICAL REVIEWS, 2012, 64 (02) :238-258
[5]
Cognitive-behavioral therapy, imipramine, or their combination for panic disorder - A randomized controlled trial [J].
Barlow, DH ;
Gorman, JM ;
Shear, MK ;
Woods, SW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (19) :2529-2536
[6]
Removing Brakes on Adult Brain Plasticity: From Molecular to Behavioral Interventions [J].
Bavelier, Daphne ;
Levi, Dennis M. ;
Li, Roger W. ;
Dan, Yang ;
Hensch, Takao K. .
JOURNAL OF NEUROSCIENCE, 2010, 30 (45) :14964-14971
[7]
Belmaker RH, 2008, NEW ENGL J MED, V358, P55, DOI [10.1056/NEJMra073096, 10.1038/nrdp.2016.65]
[8]
Molecular basis of plasticity in the visual cortex [J].
Berardi, N ;
Pizzorusso, T ;
Ratto, GM ;
Maffei, L .
TRENDS IN NEUROSCIENCES, 2003, 26 (07) :369-378
[9]
New approaches to antidepressant drug discovery: beyond monoamines [J].
Berton, O ;
Nestler, EJ .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (02) :137-151
[10]
Opinion -: Is mood chemistry? [J].
Castrén, E .
NATURE REVIEWS NEUROSCIENCE, 2005, 6 (03) :241-246