Curic Stjepan, Andreou Christina, Nolte Guido, Steinmann Saskia, Thiebes Stephanie, Polomac Nenad, Haaf Moritz, Rauh Jonas, Leicht Gregor, Mulert Christoph
Psychiatry Neuroimaging Branch, Department of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Institute for Sex Research, Sexual Medicine and Forensic Psychiatry, Center of Psychosocial Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Front Psychiatry. 2021 Jun 10;12:671007. doi: 10.3389/fpsyt.2021.671007. eCollection 2021.
Disturbed functional connectivity is assumed to cause neurocognitive deficits in patients suffering from schizophrenia. A Glutamate N-methyl-D-aspartate receptor (NMDAR) dysfunction has been suggested as a possible mechanism underlying altered connectivity in schizophrenia, especially in the gamma- and theta-frequency range. The present study aimed to investigate the effects of the NMDAR-antagonist ketamine on resting-state power, functional connectivity, and schizophrenia-like psychopathological changes in healthy volunteers. In a placebo-controlled crossover design, 25 healthy subjects were recorded using resting-state 64-channel-electroencephalography (EEG) (eyes closed). The imaginary coherence-based (MIM) was used to measure gamma and theta connectivity across 80 cortical regions. The network-based statistic was applied to identify involved networks under ketamine. Psychopathology was assessed with the Positive and Negative Syndrome Scale (PANSS) and the 5-Dimensional Altered States of Consciousness Rating Scale (5D-ASC). Ketamine caused an increase in all PANSS ( < 0.001) as well as 5D-ASC scores ( < 0.01). Significant increases in resting-state gamma and theta power were observed under ketamine compared to placebo ( < 0.05). The source-space analysis revealed two distinct networks with an increased mean functional gamma- or theta-band connectivity during the ketamine session. The gamma-network consisted of midline regions, the cuneus, the precuneus, and the bilateral posterior cingulate cortices, while the theta-band network involved the Heschl gyrus, midline regions, the insula, and the middle cingulate cortex. The current source density (CSD) within the gamma-band correlated negatively with the PANSS negative symptom score, and the activity within the gamma-band network correlated negatively with the subjective subscale of the 5D-ASC. These results are in line with resting-state patterns seen in people who have schizophrenia and argue for a crucial role of the glutamate system in mediating dysfunctional gamma- and theta-band-connectivity in schizophrenia. Resting-state networks could serve as biomarkers for the response to glutamatergic drugs or drug development efforts within the glutamate system.
功能连接紊乱被认为是导致精神分裂症患者神经认知缺陷的原因。谷氨酸N-甲基-D-天冬氨酸受体(NMDAR)功能障碍被认为是精神分裂症患者连接改变的一种可能机制,尤其是在γ和θ频率范围内。本研究旨在探讨NMDAR拮抗剂氯胺酮对健康志愿者静息态功率、功能连接以及精神分裂症样精神病理变化的影响。在安慰剂对照的交叉设计中,使用静息态64通道脑电图(EEG)(闭眼)记录25名健康受试者。基于虚部相干性(MIM)用于测量80个皮质区域之间的γ和θ连接。基于网络的统计方法用于识别氯胺酮作用下涉及的网络。使用阳性和阴性症状量表(PANSS)和5维意识状态改变评定量表(5D-ASC)评估精神病理学。氯胺酮导致所有PANSS评分(<0.001)以及5D-ASC评分(<0.01)增加。与安慰剂相比,氯胺酮作用下静息态γ和θ功率显著增加(<0.05)。源空间分析显示,在氯胺酮给药期间,有两个不同的网络平均功能γ或θ波段连接增加。γ网络由中线区域、楔叶、楔前叶和双侧后扣带回皮质组成,而θ波段网络涉及颞横回、中线区域、岛叶和中扣带回皮质。γ波段内的当前源密度(CSD)与PANSS阴性症状评分呈负相关,γ波段网络内的活动与5D-ASC的主观子量表呈负相关。这些结果与精神分裂症患者的静息态模式一致,并支持谷氨酸系统在介导精神分裂症患者功能失调的γ和θ波段连接中起关键作用。静息态网络可作为谷氨酸能药物反应或谷氨酸系统内药物开发努力的生物标志物。