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长时间清醒和恢复性睡眠对人类血清微小RNA表达谱的影响。

Prolonged Waking and Recovery Sleep Affect the Serum MicroRNA Expression Profile in Humans.

作者信息

Weigend Susanne, Holst Sebastian C, Meier Josefine, Brock Matthias, Kohler Malcolm, Landolt Hans-Peter

机构信息

Institute of Pharmacology and Toxicology, University of Zürich, 8057 Zürich, Switzerland.

Sleep and Health Zürich (SHZ), University of Zürich, 8057 Zürich, Switzerland.

出版信息

Clocks Sleep. 2018 Nov 22;1(1):75-86. doi: 10.3390/clockssleep1010008. eCollection 2019 Mar.

DOI:10.3390/clockssleep1010008
PMID:33089155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7509676/
Abstract

MicroRNAs (miRNAs) are small, abundant, non-coding RNA fragments that regulate gene expression and silencing at the post-transcriptional level. The miRNAs each control various downstream targets and play established roles in different biological processes. Given that miRNAs were recently proposed to contribute to the molecular control of sleep-wake regulation in animal models and narcoleptic patients, we investigated the impact of acute sleep deprivation on blood miRNA expression in healthy adult men of two different age groups. Twenty-two young (mean age: 24 ± 3 years) and nine older (65 ± 1 years) volunteers completed a controlled in-lab study, consisting of 8 h baseline sleep, followed by 40 h of extended wakefulness, and a 10-h recovery sleep opportunity. At the same circadian time in all three conditions (at 4:23 p.m. ± 23 min), qPCR expression profiling of 86 miRNAs was performed in blood serum. Thirteen different miRNAs could be reliably quantified and were analyzed using mixed-model ANOVAs. It was found that miR-30c and miR-127 were reliably affected by previous sleep and wakefulness, such that expression of these miRNAs was upregulated after extended wakefulness and normalized after recovery sleep. Together with previous findings in narcolepsy patients, our preliminary data indicate that miR-30c and its target proteins may provide a biomarker of elevated sleep debt in humans.

摘要

微小RNA(miRNA)是小的、丰富的非编码RNA片段,它们在转录后水平上调节基因表达和沉默。每个miRNA控制各种下游靶点,并在不同的生物学过程中发挥既定作用。鉴于最近有人提出miRNA有助于动物模型和发作性睡病患者睡眠-觉醒调节的分子控制,我们研究了急性睡眠剥夺对两个不同年龄组健康成年男性血液中miRNA表达的影响。22名年轻志愿者(平均年龄:24±3岁)和9名年长志愿者(65±1岁)完成了一项实验室对照研究,包括8小时的基线睡眠,随后是40小时的延长觉醒,以及10小时的恢复睡眠机会。在所有三种情况下的同一昼夜时间(下午4:23±23分钟),对血清中的86种miRNA进行了qPCR表达谱分析。13种不同的miRNA可以可靠地定量,并使用混合模型方差分析进行分析。结果发现,miR-30c和miR-127确实受到先前睡眠和觉醒的影响,因此这些miRNA的表达在延长觉醒后上调,在恢复睡眠后恢复正常。连同先前对发作性睡病患者的研究结果,我们的初步数据表明,miR-30c及其靶蛋白可能是人类睡眠债增加的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99fe/7509676/c73ceb8e9a41/clockssleep-01-00008-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99fe/7509676/27053c0a5013/clockssleep-01-00008-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99fe/7509676/3e4ad539d901/clockssleep-01-00008-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99fe/7509676/c73ceb8e9a41/clockssleep-01-00008-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99fe/7509676/27053c0a5013/clockssleep-01-00008-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99fe/7509676/3e4ad539d901/clockssleep-01-00008-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99fe/7509676/c73ceb8e9a41/clockssleep-01-00008-g003.jpg

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