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改变的睡眠震荡作为精神分裂症的神经生理生物标志物。

Altered Sleep Oscillations as Neurophysiological Biomarkers of Schizophrenia.

机构信息

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Adv Neurobiol. 2024;40:351-383. doi: 10.1007/978-3-031-69491-2_13.

Abstract

Sleep spindles and slow waves are the two main oscillatory activities occurring during nonrapid eye movement (NREM) sleep. Here, we will first describe the electrophysiological characteristics of these sleep oscillations along with the neurophysiological and molecular mechanisms underlying their generation and synchronization in the healthy brain. We will then review the extant evidence of deficits in sleep spindles and, to a lesser extent, slow waves, including in slow wave-spindle coupling, in patients with Schizophrenia (SCZ) across the course of the disorder, from at-risk to chronic stages. Next, we will discuss how these sleep oscillatory deficits point to defects in neuronal circuits within the thalamocortical network as well as to alterations in molecular neurotransmission implicating the GABAergic and glutamatergic systems in SCZ. Finally, after explaining how spindle and slow waves may represent neurophysiological biomarkers with predictive, diagnostic, and prognostic potential, we will present novel pharmacological and neuromodulatory interventions aimed at restoring sleep oscillatory deficits in SCZ, which in turn may serve as target engagement biomarkers to ameliorate the clinical symptoms and the quality of life of individuals affected by this devastating brain disorder.

摘要

睡眠纺锤波和慢波是在非快速眼动(NREM)睡眠期间发生的两种主要的振荡活动。在这里,我们将首先描述这些睡眠振荡的电生理特征,以及它们在健康大脑中的产生和同步的神经生理和分子机制。然后,我们将回顾现有的关于精神分裂症(SCZ)患者睡眠纺锤波和(在较小程度上)慢波缺陷的证据,包括在疾病的整个过程中,从高危期到慢性期,慢波-纺锤波耦合的缺陷。接下来,我们将讨论这些睡眠振荡缺陷如何指向丘脑皮质网络中的神经元回路的缺陷,以及涉及 GABA 能和谷氨酸能系统的分子神经传递的改变。最后,在解释了纺锤波和慢波如何可能成为具有预测、诊断和预后潜力的神经生理生物标志物之后,我们将介绍旨在恢复 SCZ 睡眠振荡缺陷的新型药物和神经调节干预措施,这反过来又可以作为目标参与生物标志物,以改善受这种破坏性大脑疾病影响的个体的临床症状和生活质量。

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