Targets and Mechanisms of Xuebijing in the Treatment of Acute Kidney Injury Associated with Sepsis: A Network Pharmacology-based Study.

IF 1.5 4区 医学 Q4 CHEMISTRY, MEDICINAL
Jing Wang, Chengyu Luo, Mengling Luo, Siwen Zhou, Guicheng Kuang
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引用次数: 0

Abstract

Introduction: Sepsis is a state of the systemic inflammatory response of the host induced by infection, frequently affecting numerous organs and producing varied degrees of damage. The most typical consequence of sepsis is sepsis-associated acute kidney injury(SA-AKI). Xuebijing is developed based on XueFuZhuYu Decoction. Five Chinese herbal extracts, including Carthami Flos, Radix Paeoniae Rubra, Chuanxiong Rhizoma, Radix Salviae, and Angelicae Sinensis Radix, make up the majority of the mixture. It has properties that are anti-inflammatory and anti-oxidative stress. Xuebijing is an effective medication for the treatment of SA-AKI, according to clinical research. But its pharmacological mechanism is still not completely understood.

Methods: First, the composition and target information of Carthami Flos, Radix Paeoniae Rubra, Chuanxiong Rhizoma, Radix Salviae, and Angelicae Sinensis Radix were collected from the TCMSP database, while the therapeutic targets of SA-AKI were exported from the gene card database. To do a GO and KEGG enrichment analysis, we first screened the key targets using a Venn diagram and Cytoscape 3.9.1. To assess the binding activity between the active component and the target, we lastly used molecular docking.

Results: For Xuebijing, a total of 59 active components and 267 corresponding targets were discovered, while for SA-AKI, a total of 1,276 targets were connected. There were 117 targets in all that was shared by goals for active ingredients and objectives for diseases. The TNF signaling pathway and the AGE-RAGE pathway were later found to be significant pathways for the therapeutic effects of Xuebijing by GO analysis and KEGG pathway analysis. Quercetin, luteolin, and kaempferol were shown to target and modulate CXCL8, CASP3, and TNF, respectively, according to molecular docking results.

Conclusion: This study predicts the mechanism of action of the active ingredients of Xuebijing in the treatment of SA-AKI, which provides a basis for future applications of Xuebijing and studies targeting the mechanism.

雪碧净治疗败血症相关急性肾损伤的靶点和机制:基于网络药理学的研究
导言:败血症是一种由感染引起的宿主全身炎症反应状态,经常影响多个器官并造成不同程度的损伤。败血症最典型的后果是败血症相关性急性肾损伤(SA-AKI)。雪碧净是在雪肤玉煎剂的基础上研制而成的。其主要成分是五种中药提取物,包括桔梗、赤芍、川芎、丹参和当归。它具有抗炎和抗氧化应激的特性。根据临床研究,雪碧是治疗 SA-AKI 的有效药物。方法:方法:首先,从中医药数据库(TCMSP)中收集荠菜、赤芍、川芎、丹参、当归的成分和靶点信息,从基因卡数据库中导出SA-AKI的治疗靶点。为了进行GO和KEGG富集分析,我们首先使用维恩图和Cytoscape 3.9.1筛选了关键靶标。为了评估活性成分与靶标之间的结合活性,我们最后使用了分子对接技术:结果:雪碧共发现了 59 种活性成分和 267 个相应的靶点,而 SA-AKI 共连接了 1,276 个靶点。活性成分目标和疾病目标共有 117 个靶点。通过GO分析和KEGG通路分析,发现TNF信号通路和AGE-RAGE通路是影响雪碧净治疗效果的重要通路。分子对接结果显示,槲皮素、木犀草素和山奈酚分别靶向调节CXCL8、CASP3和TNF:本研究预测了雪碧散有效成分在治疗SA-AKI中的作用机制,为雪碧散今后的应用和机制研究提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current computer-aided drug design
Current computer-aided drug design 医学-计算机:跨学科应用
CiteScore
3.70
自引率
5.90%
发文量
46
审稿时长
>12 weeks
期刊介绍: Aims & Scope Current Computer-Aided Drug Design aims to publish all the latest developments in drug design based on computational techniques. The field of computer-aided drug design has had extensive impact in the area of drug design. Current Computer-Aided Drug Design is an essential journal for all medicinal chemists who wish to be kept informed and up-to-date with all the latest and important developments in computer-aided methodologies and their applications in drug discovery. Each issue contains a series of timely, in-depth reviews, original research articles and letter articles written by leaders in the field, covering a range of computational techniques for drug design, screening, ADME studies, theoretical chemistry; computational chemistry; computer and molecular graphics; molecular modeling; protein engineering; drug design; expert systems; general structure-property relationships; molecular dynamics; chemical database development and usage etc., providing excellent rationales for drug development.
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