Neural circuitry and neuroplasticity in mood disorders: Insights for novel therapeutic targets

被引:113
作者
Carlson P.J. [1 ,2 ]
Singh J.B. [1 ]
Zarate Jr. C.A. [1 ]
Drevets W.C. [2 ]
Manji H.K. [1 ,3 ]
机构
[1] Laboratory of Molecular Pathophysiology, Mood and Anxiety Disorders Research Program, National Institute of Mental Health, Bethesda
[2] Section on Neuroimaging in Mood Disorders, Mood and Anxiety Disorders Research Program, National Institute of Mental Health, Bethesda
[3] MSC 3711, Building 35, Bethesda, MD 20892
来源
NeuroRX | 2006年 / 3卷 / 1期
关键词
Affective circuitry; Bipolar disorder; Brain imaging; Functional imaging; Major depressive disorder; Plasticity; Therapeutics;
D O I
10.1016/j.nurx.2005.12.009
中图分类号
学科分类号
摘要
Major depressive disorder and bipolar disorder are severe mood disorders that affect the lives and functioning of millions each year. The majority of previous neurobiological research and standard pharmacotherapy regimens have approached these illnesses as purely neurochemical disorders, with particular focus on the monoaminergic neurotransmitter systems. Not altogether surprisingly, these treatments are inadequate for many individuals afflicted with these devastating illnesses. Recent advances in functional brain imaging have identified critical neural circuits involving the amygdala and other limbic structures, prefrontal cortical regions, thalamus, and basal ganglia that modulate emotional behavior and are disturbed in primary and secondary mood disorders. Growing evidence suggests that mechanisms of neural plasticity and cellular resilience, including impairments of neurotrophic signaling cascades as well as altered glutamatergic and glucocorticoid signaling, underlie the dysregulation in these circuits. The increasing ability to monitor and modulate activity in these circuits is beginning to yield greater insight into the neurobiological basis of mood disorders. Modulation of dysregulated activity in these affective circuits via pharmacological agents that enhance neuronal resilience and plasticity, and possibly via emerging nonpharmacologic, circuitry-based modalities (for example, deep brain stimulation, magnetic stimulation, or vagus nerve stimulation) offers promising targets for novel experimental therapeutics in the treatment of mood disorders. © The American Society for Experimental NeuroTherapeutics, Inc.
引用
收藏
页码:22 / 41
页数:19
相关论文
共 173 条
[1]  
Burden of Mental and Behavioral Disorders. In the WHO Report 2001: Mental Health, New Understandings, New Hope, pp. 19-34, (2001)
[2]  
Fagiolini A., Kupfer D.J., Masalehdan A., Scott J.A., Houck P.R., Frank E., Functional impairment in the remission phase of bipolar disorder, Bipolar Disord, 7, pp. 281-285, (2005)
[3]  
Murray C.J., Lopez A.D., Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study, Lancet, 349, pp. 1436-1442, (1997)
[4]  
Revicki D.A., Matza L.S., Flood E., Lloyd A., Bipolar disorder and health-related quality of life: Review of burden of disease and clinical trials, Pharmacoeconomics, 23, pp. 583-594, (2005)
[5]  
Tohen M., Zarate Jr. Z.A., Hennen J., Et al., The McLean-Harvard First-Episode Mania Study: Prediction of recovery and first recurrence, Am J Psychiatry, 160, pp. 2099-2107, (2003)
[6]  
Ciechanowski P.S., Katon W.J., Russo J.E., Depression and diabetes: Impact of depressive symptoms on adherence, function, and costs, Arch Intern Med, 160, pp. 3278-3285, (2000)
[7]  
Kupfer D., The increasing medical burden in bipolar disorder, JAMA, 293, pp. 2528-2530, (2005)
[8]  
Michelson D., Stratakis C., Hill L., Et al., Bone mineral density in women with depression, N Engl J Med, 335, pp. 1176-1181, (1996)
[9]  
Musselman D.L., Evans D.L., Nemeroff C.B., The relationship of depression to cardiovascular disease: Epidemiology, biology, and treatment, Arch Gen Psychiatry, 55, pp. 580-592, (1998)
[10]  
Drevets W., Neuroimaging and neuropathological studies of depression: Implications for the cognitive-emotional features of mood disorders, Curr Opin Neurobiol, 11, pp. 240-249, (2001)