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独活寄生汤对骨关节炎抑制TLR4/MyD88/NF-κB信号通路的验证:一项网络药理学方法整合的实验研究

Confirmation of inhibitingTLR4/MyD88/NF-κB Signalling Pathway by Duhuo Jisheng Decoction on Osteoarthritis: A Network Pharmacology Approach-Integrated Experimental Study.

作者信息

Liu Linglong, Xu Limei, Wang Shengjie, Wang Lili, Wang Xiaoning, Xu Huifeng, Li Xihai, Ye Hongzhi

机构信息

College of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China.

Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China.

出版信息

Front Pharmacol. 2022 Jan 24;12:784822. doi: 10.3389/fphar.2021.784822. eCollection 2021.

Abstract

This study was conducted to identify whether the TLR4/MyD88/NF-κB signalling pathway plays a vital role in osteoarthritis (OA) treatment with Duhuo Jisheng Decoction (DHJSD) on the basis of a network pharmacology approach (NPA)-integrated experiment. Two experiments were conducted as follow: NPA for DHJSD using six OA-related gene series and the key pathway was screened out using NPA. NPA identified a vital role for the TLR4/MyD88/NF-κB signalling pathway in OA treatment with DHJSD, the conventional western blot analysis and qPCR confirmed it. Furthermore, changes of miR-146a-5p and miR-34a-5p in the cellular models were recovered by DHJSD administration, which synergistically contributed to OA therapy. The toll-like receptor signalling pathway and the NF-κB signalling pathway were meaningfully enriched by the miRNA-regulated gene pathways. This study identified and confirmed the TLR4/MyD88/NF-κB signalling pathway is an essential inflammatory signalling pathway in the DHJSD underlying OA treatment. The results provide a basis for further evaluation of the regulatory mechanism of the drug's efficacy in treating OA.

摘要

本研究旨在基于网络药理学方法(NPA)整合实验,确定Toll样受体4(TLR4)/髓样分化因子88(MyD88)/核因子κB(NF-κB)信号通路在独活寄生汤(DHJSD)治疗骨关节炎(OA)中是否发挥重要作用。进行了以下两个实验:使用六个与OA相关的基因系列对DHJSD进行NPA,并使用NPA筛选出关键通路。NPA确定TLR4/MyD88/NF-κB信号通路在DHJSD治疗OA中起重要作用,传统的蛋白质免疫印迹分析和定量聚合酶链反应(qPCR)证实了这一点。此外,DHJSD给药可恢复细胞模型中微小RNA-146a-5p(miR-146a-5p)和微小RNA-34a-5p(miR-34a-5p)的变化,这对OA治疗有协同作用。微小RNA调控的基因通路显著富集了Toll样受体信号通路和NF-κB信号通路。本研究确定并证实TLR4/MyD88/NF-κB信号通路是DHJSD治疗OA的重要炎症信号通路。研究结果为进一步评估该药物治疗OA疗效的调控机制提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38fa/8818874/612a70e60997/fphar-12-784822-g001.jpg

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