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睡眠障碍与代谢功能障碍中的脂肪因子:来自网络分析的见解

Adipokines in Sleep Disturbance and Metabolic Dysfunction: Insights from Network Analysis.

作者信息

Wei Zhikui, Chen You, Upender Raghu P

机构信息

Department of Neurology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37232, USA.

出版信息

Clocks Sleep. 2022 Jun 22;4(3):321-331. doi: 10.3390/clockssleep4030027.

Abstract

Adipokines are a growing group of secreted proteins that play important roles in obesity, sleep disturbance, and metabolic derangements. Due to the complex interplay between adipokines, sleep, and metabolic regulation, an integrated approach is required to better understand the significance of adipokines in these processes. In the present study, we created and analyzed a network of six adipokines and their molecular partners involved in sleep disturbance and metabolic dysregulation. This network represents information flow from regulatory factors, adipokines, and physiologic pathways to disease processes in metabolic dysfunction. Analyses using network metrics revealed that obesity and obstructive sleep apnea were major drivers for the sleep associated metabolic dysregulation. Two adipokines, leptin and adiponectin, were found to have higher degrees than other adipokines, indicating their central roles in the network. These adipokines signal through major metabolic pathways such as insulin signaling, inflammation, food intake, and energy expenditure, and exert their functions in cardiovascular, reproductive, and autoimmune diseases. Leptin, AMP activated protein kinase (AMPK), and fatty acid oxidation were found to have global influence in the network and represent potentially important interventional targets for metabolic and sleep disorders. These findings underscore the great potential of using network based approaches to identify new insights and pharmaceutical targets in metabolic and sleep disorders.

摘要

脂肪因子是一类不断增多的分泌蛋白,在肥胖、睡眠障碍和代谢紊乱中发挥重要作用。由于脂肪因子、睡眠和代谢调节之间存在复杂的相互作用,需要采用综合方法来更好地理解脂肪因子在这些过程中的重要性。在本研究中,我们构建并分析了一个由六种脂肪因子及其参与睡眠障碍和代谢失调的分子伙伴组成的网络。该网络代表了从调节因子、脂肪因子和生理途径到代谢功能障碍中疾病过程的信息流。使用网络指标进行的分析表明,肥胖和阻塞性睡眠呼吸暂停是与睡眠相关的代谢失调的主要驱动因素。发现两种脂肪因子,即瘦素和脂联素,比其他脂肪因子具有更高的度数,表明它们在网络中的核心作用。这些脂肪因子通过胰岛素信号传导、炎症、食物摄入和能量消耗等主要代谢途径发出信号,并在心血管、生殖和自身免疫性疾病中发挥作用。发现瘦素、AMP激活蛋白激酶(AMPK)和脂肪酸氧化在网络中具有全局影响,并代表了代谢和睡眠障碍潜在的重要干预靶点。这些发现强调了使用基于网络的方法在代谢和睡眠障碍中识别新见解和药物靶点的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0afd/9326621/557ae16670de/clockssleep-04-00027-g001.jpg

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