Suppr超能文献

基于系统生物学策略探讨补阳还五汤干预血管性痴呆的氧化应激机制。

Exploring the Oxidative Stress Mechanism of Buyang Huanwu Decoction in Intervention of Vascular Dementia Based on Systems Biology Strategy.

机构信息

The First Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, Hunan Province, China.

Key Lab of Hunan Province for Prevention and Treatment of Cardio-Cerebral Diseases with Integrated Traditional Chinese and Western Medicine, Hunan University of Chinese Medicine, Hunan, China.

出版信息

Oxid Med Cell Longev. 2021 Mar 3;2021:8879060. doi: 10.1155/2021/8879060. eCollection 2021.

Abstract

OBJECTIVE

To explore the oxidative stress mechanism of modified Buyang Huanwu decoction (MBHD) in intervention of vascular dementia (VD) based on systems biology strategy.

METHODS

In this study, through the reverse virtual target prediction technology and transcriptomics integration strategy, the active ingredients and potential targets of MBHD treatment of VD were analyzed, and the drug-disease protein-protein interaction (PPI) network was constructed. Then, bioinformatics analysis methods are used for Gene Ontology (GO) enrichment analysis and pathway enrichment analysis, and finally find the core biological process. After that, in animal models, low-throughput technology is used to detect gene expression and protein expression of key molecular targets in oxidative stress-mediated inflammation and apoptosis signaling pathways to verify the mechanism of MBHD treatment of VD rats. Finally, the potential interaction relationship between MBHD and VD-related molecules is further explored through molecular docking technology.

RESULTS

There are a total of 54 MBHD components, 252 potential targets, and 360 VD genes. The results of GO enrichment analysis and pathway enrichment analysis showed that MBHD may regulate neuronal apoptosis, nitric oxide synthesis and metabolism, platelet activation, NF-B signaling pathway-mediated inflammation, oxidative stress, angiogenesis, etc. Among them, SIRT1, NF-B, BAX, BCL-2, CASP3, and APP may be important targets for MBHD to treat VD. Low-throughput technology (qRT-PCR/WB/immunohistochemical technology) detects oxidative stress-mediated inflammation and apoptosis-related signaling pathway molecules. The molecular docking results showed that 64474-51-7, cycloartenol, ferulic acid, formononetin, kaempferol, liquiritigenin, senkyunone, wallichilide, xanthinin, and other molecules can directly interact with NF-B p65, BAX, BCL-2, and CASP3.

CONCLUSION

The active compounds of MBHD interact with multiple targets and multiple pathways in a synergistic manner, and have important therapeutic effects on VD mainly by balancing oxidative stress/anti-inflammatory and antiapoptotic, enhancing metabolism, and enhancing the immune system.

摘要

目的

基于系统生物学策略,探讨补阳还五汤(MBHD)干预血管性痴呆(VD)的氧化应激机制。

方法

本研究通过反向虚拟靶标预测技术和转录组学整合策略,分析 MBHD 治疗 VD 的活性成分和潜在靶标,并构建药物-疾病蛋白质-蛋白质相互作用(PPI)网络。然后,采用生物信息学分析方法进行基因本体(GO)富集分析和通路富集分析,最终找到核心生物学过程。之后,在动物模型中,采用高通量技术检测氧化应激介导的炎症和细胞凋亡信号通路中关键分子靶标基因的表达和蛋白表达,验证 MBHD 治疗 VD 大鼠的机制。最后,通过分子对接技术进一步探讨 MBHD 与 VD 相关分子的潜在相互作用关系。

结果

MBHD 共有 54 个成分,252 个潜在靶标,360 个 VD 基因。GO 富集分析和通路富集分析结果表明,MBHD 可能调节神经元凋亡、一氧化氮合成和代谢、血小板激活、NF-B 信号通路介导的炎症、氧化应激、血管生成等。其中,SIRT1、NF-B、BAX、BCL-2、CASP3、APP 可能是 MBHD 治疗 VD 的重要靶标。高通量技术(qRT-PCR/WB/免疫组化技术)检测氧化应激介导的炎症和细胞凋亡相关信号通路分子。分子对接结果表明,64474-51-7、环阿屯醇、阿魏酸、芒柄花素、山奈酚、甘草素、川芎嗪、瓦力希里定、黄嘌呤、等分子可以直接与 NF-B p65、BAX、BCL-2、和 CASP3。

结论

MBHD 的活性化合物以协同方式与多个靶点和多条通路相互作用,通过平衡氧化应激/抗炎和抗凋亡、增强代谢和增强免疫系统,对 VD 具有重要的治疗作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验