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应激诱导的大鼠脑区蛋白质组及网络分析鉴定抗抑郁/焦虑潜在药物靶点

The Identification of Potential Anti-Depression/Anxiety Drug Targets by Stress-Induced Rat Brain Regional Proteome and Network Analyses.

机构信息

Institute of Neuroscience, School of Basic Medical Sciences, Chongqing Medical University, 1 Yixueyuan Road, Yuzhong District, Chongqing, 400016, China.

Department of Neurology, The Second Affiliated Hospital of Nanchang University, 1 Minde Road, Nanchang, 330006, Jiangxi, People's Republic of China.

出版信息

Neurochem Res. 2024 Oct;49(10):2957-2971. doi: 10.1007/s11064-024-04220-x. Epub 2024 Aug 1.

Abstract

Depression and anxiety disorders are prevalent stress-related neuropsychiatric disorders and involve multiple molecular changes and dysfunctions across various brain regions. However, the specific and shared pathophysiological mechanisms occurring in these regions remain unclear. Previous research used a rat model of chronic mild stress (CMS) to segregate and identify depression-susceptible, anxiety-susceptible, and insusceptible groups; then the proteomes of six distinct brain regions (the hippocampus, prefrontal cortex, hypothalamus, pituitary, olfactory bulb, and striatum) were separately and quantitatively analyzed. To gain a comprehensive and systematic understanding of the molecular abnormalities, this study aimed to investigate and compare differential proteomics data from the six regions. Differentially expressed proteins (DEPs) were identified in between specific regions and across all regions and subjected to a series of bioinformatics analyses. Regional comparisons showed that stress-induced proteomic changes and corresponding gene ontology and pathway enrichments were largely distinct, attributable to differences in cell populations, protein compositions, and brain functions of these areas. Additionally, a notable degree of overlap in the significantly enriched terms was identified, potentially suggesting strong connections in the enrichment across different regions. Furthermore, intra-regional and inter-regional protein-protein interaction networks and drug-target-DEP networks were constructed. Integrated analysis of the three association networks in the six regions, along with the DisGeNET database, identified ten DEPs as potential targets for anti-depression/anxiety drugs. Collectively, these findings revealed commonalities and differences across different brain regions at the protein level induced by CMS, and identified several novel protein targets for the development of new therapeutics for depression and anxiety.

摘要

抑郁和焦虑障碍是常见的应激相关神经精神障碍,涉及多个大脑区域的多种分子变化和功能障碍。然而,这些区域中发生的特定和共享的病理生理机制尚不清楚。先前的研究使用慢性轻度应激(CMS)大鼠模型来分离和鉴定易患抑郁、易患焦虑和不易患的组;然后分别定量分析了六个不同脑区(海马体、前额叶皮层、下丘脑、垂体、嗅球和纹状体)的蛋白质组。为了全面系统地了解分子异常,本研究旨在研究和比较来自六个区域的差异蛋白质组学数据。在特定区域之间和所有区域之间鉴定出差异表达蛋白(DEPs),并进行了一系列生物信息学分析。区域比较表明,应激诱导的蛋白质组变化及其对应的基因本体和途径富集在很大程度上是不同的,这归因于这些区域的细胞群体、蛋白质组成和脑功能的差异。此外,还发现显著富集术语之间存在显著重叠,这可能表明不同区域之间的富集存在很强的联系。此外,构建了区域内和区域间蛋白质-蛋白质相互作用网络以及药物-靶标-DEP 网络。对六个区域的三个关联网络进行综合分析,并结合 DisGeNET 数据库,确定了十个 DEPs 作为抗抑郁/抗焦虑药物的潜在靶点。综上所述,这些发现揭示了 CMS 诱导的不同大脑区域在蛋白质水平上的共性和差异,并确定了几个新的蛋白质靶点,用于开发治疗抑郁和焦虑的新疗法。

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