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Metabolomics-based profiling of anti-inflammatory compounds from in shanghe, China. | LitMetric

Metabolomics-based profiling of anti-inflammatory compounds from in shanghe, China.

Heliyon

Engineering Research Center of Zebrafish Models for Human Diseases and Drug Screening, Biology Institute, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250103, China.

Published: August 2024

AI Article Synopsis

Article Abstract

is a popular herb used in foods, cosmetics, and medicines. In the present study, liquid chromatography-mass spectrometry-based metabolomics analysis and the zebrafish model were used to investigate the potential biomarkers of growing in Shanghe County (Shandong Province, China) and their anti-inflammatory properties. Network pharmacology and molecular docking were performed to screen the main targets of the characteristic compounds to understand their mechanisms of action. Nine potential markers including sugars (,), polyphenolic acids (-), and flavonoids (-) were identified from the species. The inhibitory effects on leukocyte migration confirmed that compounds and - played a positive role in the protective effect of Shanghe (SM) extract against inflammation. Akt (protein kinase B), EGFR (epidermal growth factor receptor), and MMP9 (matrix metalloproteinase 9) were the core target proteins of the identified compounds in the anti-inflammatory process. The most significant Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment terms were response to abiotic stimulus (Biological Process), carbohydrate derivative binding (Molecular Function), and pathways in cancer. In docking simulations, 3-p-coumaroylquinic acid (3-PC, ) and cirsimaritin (CN, ) exhibited the highest potential affinity to the active sites of Akt and EGFR proteins, respectively; additionally, 5-demethylsinensetin (5-DS, ) and luteolin (LN, ) were considered the most suitable ligands for the MMP9 protein. The present study highlighted the use of SM resources as functional products with health benefits.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11365440PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e35974DOI Listing

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