The Sesquiterpene, Selin-11-en-4α-ol, from Artemisia vulgaris Inhibits Lipopolysaccharide-Induced Inflammatory Responses in RAW264.7 Cells via MAPK and NF-κB Signaling Pathways

Author:

Wei Ning12ORCID,Dong Wanwen12,Liu Tao23,Guo Yuying2,Liang Feng2,You Yuejiao1,Ye Cuifang45,Wang Yifei3,Wang Qiaoli2,Wang Zhiping1

Affiliation:

1. Guangdong Provincial Key Laboratory of Advanced Drug Delivery Systems and Guangdong Provincial Engineering Center of Topical Precise Drug Delivery System, School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, China

2. GuangZhou (Jinan) Biomedical Research and Development Center Co. Ltd, Guangzhou, China

3. Department of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, China

4. Key Laboratory of Innovative Technology Research on Natural Products and Cosmetics Raw Materials, Guangzhou, China

5. Guangdong Provincial Biotechnology Drug & Engineering Technology Research Center, Guangzhou, China

Abstract

Objective Our study aimed to investigate the underlying molecular mechanisms of selin-11-en-4α-ol purified from Artemisia vulgaris against anti-inflammation through network pharmacology, molecular docking, and in vitro experiments. Methods Potential targets for selin-11-en-4α-ol and inflammation were obtained using Swiss Target Prediction, Pharm Mapper, and GeneCards databases. Venn diagrams were used to obtain the targets of selin-11-en-4α-ol for the treatment of inflammation, and the intersecting targets were uploaded to the STRING database to construct a protein–protein interaction (PPI) network of selin-11-en-4α-ol anti-inflammatory target proteins for further screening of the core targets. The Gene Ontology and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were conducted using the DAVID database. In addition, molecular docking validation of core target binding to selin-11-en-4α-ol was performed. The anti-inflammatory effects were verified by in vitro experiments of lipopolysaccharide-induced RAW264.7 cells. Results PPI network analysis showed that mitogen-activated protein kinase 14 (MAPK14), SRC, and HSP90AA1 were predicted as potential anti-inflammatory targets, and KEGG enrichment analysis revealed that the MAPK signaling pathway presented the highest gene enrichment counts. Molecular docking and western blot results suggested that selin-11-en-4α-ol regulated MAPK and nuclear transcription factor-κB (NF-κB) signaling pathways to alleviate inflammation. In addition, selin-11-en-4α-ol inhibited the production of inflammatory factors, chemokines, and reactive oxygen species and exhibited anti-inflammatory and antioxidant effects. Conclusion Selin-11-en-4α-ol treats inflammation by targeting the MAPK and NF-κB signaling pathway, demonstrating that network pharmacology and molecular docking are effective tools for studying traditional Chinese medicine and providing a theoretical basis for developing anti-inflammatory drugs.

Funder

Guangzhou key research and development plan

Guangdong Modern Agricultural Industrial Technology System Innovation Team Project

Undergraduate Innovation and Entrepreneurship Training Program of Guangdong Pharmaceutical University

Guangdong Province ordinary universities characteristic innovation project

Publisher

SAGE Publications

Subject

Complementary and alternative medicine,Plant Science,Drug Discovery,Pharmacology,General Medicine

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