The Molecular Mechanism of Resveratrol in the Treatment of Chronic Rhinosinusitis Through a Combination of Network Pharmacology and In Vitro Validation

IF 3.3 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiao Cheng, Shanshan Xu, Furong Han, Zhihui Song, Jiawei Wang
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Abstract

Resveratrol (RES) is a polyphenolic antioxidant derived from different plant products, which has anti-inflammatory and antioxidative stress effect. However, the effect of resveratrol on chronic rhinosinusitis (CRS) still lacks systematic research. This study aims to elucidate the potential mechanism of resveratrol against CRS disease through network pharmacology and further verify it through biological experiments in human nasal epithelial cells (HNEpCs). The potential targets and pathways of RES against CRS disease were predicted by network pharmacology and molecular docking. Furthermore, the inflammation of HNEpCs was induced by lipopolysaccharide (LPS). The method of ELISA was used to detect changes in inflammatory factors and oxidative stress-related factors. The RT-qPCR method was adopted to analyze the changes of genes in related signaling pathways. As a result, 33 potential targets related to the effect of RES against CRS disease were obtained. According to the results of network pharmacology, it was shown that the effect of RES against CRS disease was closely related to the inflammation, oxidative stress, and apoptosis. A variety of results from cell experiments verified that RES can effectively inhibit the inflammation, oxidative stress and apoptosis of LPS-induced HNEpCs. Together, the present study systematically clarified the possible mechanisms of RES in the treatment of CRS and provided new ideas for the drug research of this disease.

Abstract Image

网络药理与体外验证相结合研究白藜芦醇治疗慢性鼻窦炎的分子机制
白藜芦醇(Resveratrol, RES)是一种从多种植物中提取的多酚类抗氧化剂,具有抗炎和抗氧化应激作用。然而,白藜芦醇对慢性鼻窦炎(CRS)的影响尚缺乏系统的研究。本研究旨在通过网络药理学阐明白藜芦醇抗CRS病的潜在机制,并通过人鼻上皮细胞(HNEpCs)生物学实验进一步验证。通过网络药理学和分子对接预测了RES对CRS病的潜在靶点和通路。此外,脂多糖(LPS)可诱导HNEpCs的炎症反应。采用ELISA法检测炎症因子及氧化应激相关因子的变化。采用RT-qPCR方法分析相关信号通路中基因的变化。由此获得了33个与RES抗CRS疾病作用相关的潜在靶点。网络药理学结果表明,RES抗CRS病的作用与炎症、氧化应激和细胞凋亡密切相关。多种细胞实验结果证实,RES能有效抑制lps诱导的HNEpCs的炎症、氧化应激和凋亡。本研究系统阐明了RES治疗CRS的可能机制,为CRS的药物研究提供了新的思路。
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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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