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睡眠剥夺应激的系统性和局部代谢改变:基于多平台质谱的脂质组学和代谢组学方法。

Systemic and Local Metabolic Alterations in Sleep-Deprivation-Induced Stress: A Multiplatform Mass-Spectrometry-Based Lipidomics and Metabolomics Approach.

机构信息

College of Pharmacy , Seoul National University , Seoul 08826 , Republic of Korea.

Department of Biomedical Sciences, College of Medicine , Inha University , Incheon 22212 , Republic of Korea.

出版信息

J Proteome Res. 2019 Sep 6;18(9):3295-3304. doi: 10.1021/acs.jproteome.9b00234. Epub 2019 Jul 31.

DOI:10.1021/acs.jproteome.9b00234
PMID:31313932
Abstract

Sleep deprivation (SD) is known to be associated with metabolic disorders and chronic diseases. Complex metabolic alterations induced by SD at omics scale and the associated biomarker candidates have been proposed. However, in vivo systemic and local metabolic shift patterns of the metabolome and lipidome in acute and chronic partial SD models remain to be elucidated. In the present study, the serum, hypothalamus, and hippocampus CA1 of sleep-deprived rats (SD rats) from acute and chronic sleep restriction models were analyzed using three different omics platforms for the discovery and mechanistic assessment of systemic and local SD-induced dysregulated metabolites. We found a similar pattern of systemic metabolome alterations between two models, for which the area under the curve (AUC) of receiver operating characteristic curves was AUC = 0.847 and 0.930 with the pseudotargeted and untargeted metabolomics approach, respectively. However, SD-induced systemic lipidome alterations were significantly different and appeared to be model-dependent (AUC = 0.374). Comprehensive pathway analysis of the altered lipidome and metabolome in the hypothalamus indicated the abnormal behavior of eight metabolic and lipid metabolic pathways. The metabolic alterations of the hippocampus CA1 was subtle in two SD models. Collectively, these results extend our understanding of the quality of sleep and suggest metabolic targets in developing diagnostic biomarkers for better SD control.

摘要

睡眠剥夺(SD)与代谢紊乱和慢性疾病有关。已经提出了 SD 在组学水平上引起的复杂代谢变化和相关的生物标志物候选物。然而,急性和慢性部分 SD 模型中代谢组学和脂质组学的全身和局部代谢转移模式仍有待阐明。在本研究中,使用三种不同的组学平台分析了急性和慢性睡眠限制模型中睡眠剥夺大鼠(SD 大鼠)的血清、下丘脑和海马 CA1,以发现和评估全身和局部 SD 诱导的代谢物失调的机制。我们发现两种模型之间存在相似的系统代谢组改变模式,其中基于伪靶向和非靶向代谢组学方法的曲线下面积(AUC)分别为 AUC = 0.847 和 0.930。然而,SD 诱导的全身脂质组改变则存在显著差异,且似乎依赖于模型(AUC = 0.374)。对下丘脑改变的脂质组和代谢组进行的综合途径分析表明,八种代谢和脂质代谢途径的异常行为。两种 SD 模型中海马 CA1 的代谢改变较为细微。总之,这些结果扩展了我们对睡眠质量的理解,并为开发更好的 SD 控制诊断生物标志物提供了代谢靶标。

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