The role of cortical inhibition in the pathophysiology and treatment of schizophrenia

被引:88
作者
Daskalakis, Zafiris J. [1 ]
Fitzgerald, Paul B. [2 ]
Christensen, Bruce K. [1 ]
机构
[1] Univ Toronto, Dept Psychiat, Ctr Addict & Mental Hlth, Dept Psychiat,Schizophrenia Program, Toronto, ON, Canada
[2] Alfred & Monash Univ, Dept Psychol Med, Alfred Psychiat Res Ctr, Melbourne, Vic, Australia
基金
加拿大健康研究院; 英国医学研究理事会;
关键词
schizophrenia; transcranial magnetic stimulation; inhibition cortex; GABA; antipsychotic; interneuron;
D O I
10.1016/j.brainresrev.2007.09.006
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Dysfunctional cortical inhibition (CI) has been suggested as a mechanism through which symptoms of schizophrenia (SCZ) are mediated. Cortical inhibition refers to a neurophysiological process in which gamma-aminobutyric acid (GABA) inhibitory interneurons selectively attenuate the activity of other neurons (e.g., pyramidal neurons) in the cortex. Here we review the neuroanatomic and neurophysiological evidence suggesting CI deficits among persons with SCZ. We also review genetic studies that have linked CI deficits to a polymorphism in the alpha(7)-nicotinic cholinergic receptor, thereby positing that a specific genetic mechanism underlies SCZ-related GABA interneuron dysfunction. We will conclude by reviewing the role of CI as a mechanism mediating the therapeutic action of antipsychotic medications. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:427 / 442
页数:16
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