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电压门控离子通道与睡眠。

Voltage Gated Ion Channels and Sleep.

机构信息

Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai, 200240, China.

Faculty of Brain Sciences, University College London, London, UK.

出版信息

J Membr Biol. 2024 Dec;257(5-6):269-280. doi: 10.1007/s00232-024-00325-0. Epub 2024 Oct 1.

DOI:10.1007/s00232-024-00325-0
PMID:39354150
Abstract

Ion channels are integral components of the nervous system, playing a pivotal role in shaping membrane potential, neuronal excitability, synaptic transmission and plasticity. Dysfunction in these channels, such as improper expression or localization, can lead to irregular neuronal excitability and synaptic communication, which may manifest as various behavioral abnormalities, including disrupted rest-activity cycles. Research has highlighted the significant impact of voltage gated ion channels on sleep parameters, influencing sleep latency, duration and waveforms. Furthermore, these ion channels have been implicated in the vulnerability to, and the pathogenesis of, several neurological and psychiatric disorders, including epilepsy, autism, schizophrenia, and Alzheimer's disease (AD). In this comprehensive review, we aim to provide a summary of the regulatory role of three predominant types of voltage-gated ion channels-calcium (Ca), sodium (Na), and potassium (K)-in sleep across species, from flies to mammals. We will also discuss the association of sleep disorders with various human diseases that may arise from the dysfunction of these ion channels, thereby underscoring the potential therapeutic benefits of targeting specific ion channel subtypes for sleep disturbance treatment.

摘要

离子通道是神经系统的重要组成部分,在调节膜电位、神经元兴奋性、突触传递和可塑性方面发挥着关键作用。这些通道的功能障碍,如表达或定位异常,可能导致神经元兴奋性和突触通讯异常,表现为各种行为异常,包括休息-活动周期紊乱。研究表明,电压门控离子通道对睡眠参数有重要影响,影响睡眠潜伏期、持续时间和波形。此外,这些离子通道与多种神经和精神疾病的易感性和发病机制有关,包括癫痫、自闭症、精神分裂症和阿尔茨海默病(AD)。在这篇全面的综述中,我们旨在总结钙(Ca)、钠(Na)和钾(K)三种主要类型的电压门控离子通道在从苍蝇到哺乳动物的各种物种中的睡眠调节作用。我们还将讨论与各种人类疾病相关的睡眠障碍,这些疾病可能是由于这些离子通道的功能障碍引起的,从而强调针对特定离子通道亚型治疗睡眠障碍的潜在治疗益处。

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本文引用的文献

1
Potassium and calcium channels in different nerve cells act as therapeutic targets in neurological disorders.不同神经细胞中的钾通道和钙通道可作为神经疾病的治疗靶点。
Neural Regen Res. 2025 May 1;20(5):1258-1276. doi: 10.4103/NRR.NRR-D-23-01766. Epub 2024 Jun 3.
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Oxidative stress and ion channels in neurodegenerative diseases.神经退行性疾病中的氧化应激与离子通道
Front Physiol. 2024 Jan 29;15:1320086. doi: 10.3389/fphys.2024.1320086. eCollection 2024.
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Resveratrol and Sir2 Reverse Sleep and Memory Defects Induced by Amyloid Precursor Protein.
白藜芦醇和 Sir2 逆转淀粉样前体蛋白引起的睡眠和记忆缺陷。
Neurosci Bull. 2023 Jul;39(7):1117-1130. doi: 10.1007/s12264-023-01056-3. Epub 2023 Apr 11.
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The importance of ligand gated ion channels in sleep and sleep disorders.配体门控离子通道在睡眠和睡眠障碍中的重要性。
Biochem Pharmacol. 2023 Jun;212:115532. doi: 10.1016/j.bcp.2023.115532. Epub 2023 Apr 3.
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Potassium channels and epilepsy.钾通道与癫痫。
Acta Neurol Scand. 2022 Dec;146(6):699-707. doi: 10.1111/ane.13695. Epub 2022 Oct 12.
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Upregulation of IP receptor mediates APP-induced defects in synaptic downscaling and sleep homeostasis.IP 受体的上调介导了 APP 诱导的突触缩小缺陷和睡眠稳态失衡。
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Deficiency of autism-related Scn2a gene in mice disrupts sleep patterns and circadian rhythms.自闭症相关 Scn2a 基因缺失的小鼠会扰乱睡眠模式和昼夜节律。
Neurobiol Dis. 2022 Jun 15;168:105690. doi: 10.1016/j.nbd.2022.105690. Epub 2022 Mar 14.
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Na1.1 haploinsufficiency impairs glutamatergic and GABAergic neuron function in the thalamus.Na1.1 杂合性缺失损害丘脑谷氨酸能和 GABA 能神经元功能。
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Hyperexcitable arousal circuits drive sleep instability during aging.过度兴奋的唤醒回路导致衰老过程中的睡眠不稳定。
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Sleep, circadian rhythm and gut microbiota: alterations in Alzheimer's disease and their potential links in the pathogenesis.睡眠、昼夜节律和肠道微生物群:阿尔茨海默病中的改变及其在发病机制中的潜在联系。
Gut Microbes. 2021 Jan-Dec;13(1):1957407. doi: 10.1080/19490976.2021.1957407.