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

IF 3.7 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Neurochemical Research Pub Date : 2024-08-01 DOI:10.1007/s11064-024-04220-x
Nan Liu, Jiaxin Tu, Faping Yi, Xiong Zhang, Xianhui Zhong, Lili Wang, Liang Xie, Jian Zhou
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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.

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通过应激诱导的大鼠脑区域蛋白质组和网络分析确定潜在的抗抑郁/焦虑药物靶点
抑郁症和焦虑症是普遍存在的与压力有关的神经精神疾病,涉及多个脑区的多种分子变化和功能障碍。然而,发生在这些区域的特定和共同的病理生理机制仍不清楚。之前的研究利用慢性轻度应激(CMS)大鼠模型来分离和识别抑郁易感组、焦虑易感组和不易感组,然后分别对六个不同脑区(海马、前额叶皮层、下丘脑、垂体、嗅球和纹状体)的蛋白质组进行定量分析。为了全面系统地了解分子异常,本研究旨在调查和比较六个区域的差异蛋白质组学数据。研究人员对特定区域之间和所有区域之间的差异表达蛋白(DEPs)进行了鉴定,并进行了一系列生物信息学分析。区域比较显示,应激诱导的蛋白质组变化以及相应的基因本体论和通路富集在很大程度上是不同的,这归因于这些区域的细胞群、蛋白质组成和大脑功能的差异。此外,在显著富集的术语中还发现了明显的重叠,这可能表明不同区域的富集存在密切联系。此外,还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-靶点-DEP网络。通过对六个区域的三个关联网络以及 DisGeNET 数据库进行综合分析,确定了十个 DEPs 作为抗抑郁/焦虑药物的潜在靶点。总之,这些发现揭示了不同脑区在 CMS 诱导的蛋白质水平上的共性和差异,并为开发治疗抑郁症和焦虑症的新疗法确定了几个新的蛋白质靶点。
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来源期刊
Neurochemical Research
Neurochemical Research 医学-神经科学
CiteScore
7.70
自引率
2.30%
发文量
320
审稿时长
6 months
期刊介绍: Neurochemical Research is devoted to the rapid publication of studies that use neurochemical methodology in research on nervous system structure and function. The journal publishes original reports of experimental and clinical research results, perceptive reviews of significant problem areas in the neurosciences, brief comments of a methodological or interpretive nature, and research summaries conducted by leading scientists whose works are not readily available in English.
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