Radhu Natasha, Garcia Dominguez Luis, Farzan Faranak, Richter Margaret A, Semeralul Mawahib O, Chen Robert, Fitzgerald Paul B, Daskalakis Zafiris J
1 Temerty Centre for Therapeutic Brain Intervention, Centre for Addiction and Mental Health, University of Toronto, Toronto, Ontario, Canada.
2 Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
Brain. 2015 Feb;138(Pt 2):483-97. doi: 10.1093/brain/awu360. Epub 2014 Dec 17.
Abnormal gamma-aminobutyric acid inhibitory neurotransmission is a key pathophysiological mechanism underlying schizophrenia. Transcranial magnetic stimulation can be combined with electroencephalography to index long-interval cortical inhibition, a measure of GABAergic receptor-mediated inhibitory neurotransmission from the frontal and motor cortex. In previous studies we have reported that schizophrenia is associated with inhibitory deficits in the dorsolateral prefrontal cortex compared to healthy subjects and patients with bipolar disorder. The main objective of the current study was to replicate and extend these initial findings by evaluating long-interval cortical inhibition from the dorsolateral prefrontal cortex in patients with schizophrenia compared to patients with obsessive-compulsive disorder. A total of 111 participants were assessed: 38 patients with schizophrenia (average age: 35.71 years, 25 males, 13 females), 27 patients with obsessive-compulsive disorder (average age: 36.15 years, 11 males, 16 females) and 46 healthy subjects (average age: 33.63 years, 23 females, 23 males). Long-interval cortical inhibition was measured from the dorsolateral prefrontal cortex and motor cortex through combined transcranial magnetic stimulation and electroencephalography. In the dorsolateral prefrontal cortex, long-interval cortical inhibition was significantly reduced in patients with schizophrenia compared to healthy subjects (P = 0.004) and not significantly different between patients with obsessive-compulsive disorder and healthy subjects (P = 0.5445). Long-interval cortical inhibition deficits in the dorsolateral prefrontal cortex were also significantly greater in patients with schizophrenia compared to patients with obsessive-compulsive disorder (P = 0.0465). There were no significant differences in long-interval cortical inhibition across all three groups in the motor cortex. These results demonstrate that long-interval cortical inhibition deficits in the dorsolateral prefrontal cortex are specific to patients with schizophrenia and are not a generalized deficit that is shared by disorders of severe psychopathology.
异常的γ-氨基丁酸抑制性神经传递是精神分裂症潜在的关键病理生理机制。经颅磁刺激可与脑电图相结合,以评估长时程皮层抑制,这是一种衡量来自额叶和运动皮层的γ-氨基丁酸能受体介导的抑制性神经传递的指标。在之前的研究中,我们报告称,与健康受试者和双相情感障碍患者相比,精神分裂症与背外侧前额叶皮层的抑制缺陷有关。本研究的主要目的是通过评估精神分裂症患者与强迫症患者背外侧前额叶皮层的长时程皮层抑制,来重复和扩展这些初步发现。总共评估了111名参与者:38名精神分裂症患者(平均年龄:35.71岁,男性25名,女性13名),27名强迫症患者(平均年龄:36.15岁,男性11名,女性16名)和46名健康受试者(平均年龄:33.63岁,女性23名,男性23名)。通过联合经颅磁刺激和脑电图,从背外侧前额叶皮层和运动皮层测量长时程皮层抑制。在背外侧前额叶皮层,与健康受试者相比,精神分裂症患者的长时程皮层抑制显著降低(P = 0.004),强迫症患者与健康受试者之间无显著差异(P = 0.5445)。与强迫症患者相比,精神分裂症患者背外侧前额叶皮层的长时程皮层抑制缺陷也显著更大(P = 0.0465)。在运动皮层,三组之间的长时程皮层抑制没有显著差异。这些结果表明,背外侧前额叶皮层的长时程皮层抑制缺陷是精神分裂症患者所特有的,并非严重精神病理学障碍所共有的普遍缺陷。