Department of Neurosurgery, The Affiliated People's Hospital of NingBo University, NingBo, China.
Synapse. 2022 Sep;76(11-12):e22247. doi: 10.1002/syn.22247. Epub 2022 Aug 1.
Brain oscillations have gained great attention in neuroscience during recent decades as functional building blocks of cognitive-sensory processes. Research has shown that oscillations in "alpha," "beta," "gamma," "delta," and "theta" frequency windows are highly modified in brain pathology, including in patients with cognitive impairment like bipolar disorder (BD). The study of changes in brain oscillations can provide fundamental knowledge for exploring neurophysiological biomarkers in cognitive impairment. The present article reviews findings from the role and molecular basis of abnormal neural oscillation and synchronization in the symptoms of patients with BD. An overview of the results clearly demonstrates that, in cognitive-sensory processes, resting and evoked/event-related electroencephalogram (EEG) spectra in the delta, theta, alpha, beta, and gamma bands are abnormally changed in patients with BD showing psychotic features. Abnormal oscillations have been found to be associated with several neural dysfunctions and abnormalities contributing to BD, including abnormal GABAergic neurotransmission signaling, hippocampal cell discharge, abnormal hippocampal neurogenesis, impaired cadherin and synaptic contact-based cell adhesion processes, extended lateral ventricles, decreased prefrontal cortical gray matter, and decreased hippocampal volume. Mechanistically, impairment in calcium voltage-gated channel subunit alpha1 I, neurotrophic tyrosine receptor kinase proteins, genes involved in brain neurogenesis and synaptogenesis like WNT3 and ACTG2, genes involved in the cell adhesion process like CDH12 and DISC1, and gamma-aminobutyric acid (GABA) signaling have been reported as the main molecular contributors to the abnormalities in resting-state low-frequency oscillations in BD patients. Findings also showed the association of impaired synaptic connections and disrupted membrane potential with abnormal beta/gamma oscillatory activity in patients with BD. Of note, the synaptic GABA neurotransmitter has been found to be a fundamental requirement for the occurrence of long-distance synchronous gamma oscillations necessary for coordinating the activity of neural networks between various brain regions.
脑振荡在最近几十年的神经科学中引起了极大的关注,因为它们是认知-感觉过程的功能构建块。研究表明,在脑病理学中,包括在认知障碍(如双相情感障碍)的患者中,“阿尔法”、“贝塔”、“伽马”、“德尔塔”和“西塔”频率窗口中的振荡高度改变。对脑振荡变化的研究可以为探索认知障碍中的神经生理学生物标志物提供基础知识。本文综述了异常神经振荡和同步在双相情感障碍患者症状中的作用和分子基础的研究结果。结果清楚地表明,在认知-感觉过程中,具有精神病特征的双相情感障碍患者的静息和诱发/事件相关脑电图(EEG)频谱在 delta、theta、alpha、beta 和 gamma 频段中异常改变。异常振荡已被发现与双相情感障碍中的几种神经功能障碍和异常有关,包括异常的 GABA 能神经传递信号、海马细胞放电、异常的海马神经发生、细胞黏附过程中钙黏蛋白和突触接触的异常、侧脑室扩张、前额叶皮质灰质减少和海马体积减少。在机制上,钙电压门控通道亚单位 alpha1 I 的损伤、神经营养酪氨酸受体激酶蛋白、涉及脑神经发生和突触发生的基因(如 WNT3 和 ACTG2)、涉及细胞黏附过程的基因(如 CDH12 和 DISC1)以及γ-氨基丁酸(GABA)信号转导被报道为双相情感障碍患者静息状态低频振荡异常的主要分子贡献者。研究结果还表明,在双相情感障碍患者中,突触连接受损和膜电位改变与异常的 beta/gamma 振荡活动有关。值得注意的是,突触 GABA 神经递质已被发现是发生长距离同步 gamma 振荡的基本要求,这种振荡对于协调不同大脑区域之间的神经网络活动是必要的。