双相情感障碍患者异常脑振荡与认知表现之间的关系:分子机制和临床证据。

IF 1.6 4区 医学 Q4 NEUROSCIENCES
Synapse Pub Date : 2022-09-01 Epub Date: 2022-08-01 DOI:10.1002/syn.22247
Zhou Lu, Huixiao Wang, Jiajie Gu, Feng Gao
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引用次数: 3

摘要

近几十年来,脑振荡作为认知-感觉过程的功能组成部分,在神经科学领域受到了极大的关注。研究表明,“α”、“β”、“γ”、“δ”和“θ”频率窗口的振荡在脑部病理中是高度改变的,包括双相情感障碍(BD)等认知障碍患者。脑振荡变化的研究可以为探索认知障碍的神经生理生物标志物提供基础知识。本文从异常神经振荡和同步在双相障碍患者症状中的作用和分子基础方面综述了研究结果。研究结果清楚地表明,在认知-感觉过程中,表现出精神病性特征的双相障碍患者的静息和诱发/事件相关脑电图(EEG)频谱在δ、θ、α、β和γ波段发生异常改变。研究发现,异常振荡与几种导致双相障碍的神经功能障碍和异常有关,包括gaba能神经传递信号异常、海马细胞放电、海马神经发生异常、钙粘蛋白和突触接触细胞粘附过程受损、侧脑室延长、前额叶皮层灰质减少和海马体积减少。从机制上讲,钙电压门控通道亚基α 1 I、神经营养酪氨酸受体激酶蛋白、参与脑神经发生和突触发生的基因如WNT3和ACTG2、参与细胞粘附过程的基因如CDH12和DISC1以及γ -氨基丁酸(GABA)信号通路的损伤是导致BD患者静息状态低频振荡异常的主要分子因素。研究结果还显示,突触连接受损和膜电位破坏与BD患者异常的β / γ振荡活动有关。值得注意的是,突触GABA神经递质已被发现是协调大脑各区域之间神经网络活动所必需的长距离同步伽马振荡发生的基本要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association between abnormal brain oscillations and cognitive performance in patients with bipolar disorder: Molecular mechanisms and clinical evidence.

Association between abnormal brain oscillations and cognitive performance in patients with bipolar disorder: Molecular mechanisms and clinical evidence.

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.

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来源期刊
Synapse
Synapse 医学-神经科学
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
4-8 weeks
期刊介绍: SYNAPSE publishes articles concerned with all aspects of synaptic structure and function. This includes neurotransmitters, neuropeptides, neuromodulators, receptors, gap junctions, metabolism, plasticity, circuitry, mathematical modeling, ion channels, patch recording, single unit recording, development, behavior, pathology, toxicology, etc.
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