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Journal of Chinese Pharmaceutical Sciences ›› 2024, Vol. 33 ›› Issue (7): 631-646.DOI: 10.5246/jcps.2024.07.047

• Original articles • Previous Articles     Next Articles

A network pharmacological study to investigate the combination of LHQW-XYS in the treatment of COVID-19 olfactory impairment-associated

Xiaoyu Wei1,#, Luhang Yu2,#, Mengru Li3,#, Qiang Xu4,*()   

  1. 1 Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China
    2 Chinese PLA Medical School, Chinese People’s Liberation Army (PLA) General Hospital, Beijing 100853, China
    3 First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300381, China
    4 Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300250, China
  • Received:2023-12-21 Revised:2024-01-23 Accepted:2024-03-12 Online:2024-07-30 Published:2024-07-30
  • Contact: Qiang Xu
  • About author:

    # Xiaoyu Wei, Luhang Yu and Mengru Li contributed equally to this work.

  • Supported by:
    National Natural Science Foundation of China General Project (Grant No. 82374195).

Abstract:

To explore the target of action of LHQW-XYS on the main components of COVID-19 olfactory impairment by using network pharmacological methods and try to reveal its mechanism of action in the treatment related to COVID-19 induced olfactory impairment, we used the TCMSP platform to obtain potential active ingredients through oral utilization and drug-like properties screening; the Swiss TargetPrediction platform to predict the targets of the active ingredients and construct a drug-ingredient-target network, and then obtained the gene targets of COVID-19 olfactory injury through GeneCards, OMIM, and TTD platforms to intersect the drug targets and disease genes to obtain common targets. The drug targets and disease genes were intersected to obtain common targets. STRING and Cytoscape 3.8.2 software were used to construct the target-disease gene PPI network, screen the key targets and core gene clusters, and analyze the key targets by GO and KEGG enrichment analyses with the help of the Metascape platform, and then map the screened core active ingredients and their targets into the pathway to construct the core active ingredients-targets-pathway network. The core active ingredient-target-pathway network was constructed, and finally, molecular docking was carried out. The results showed that there were 4669 potential targets, 5609 disease targets, and 17 drug-disease cross-targets for the active ingredients of LHQW-XYS. The GO and KEGG enrichment analyses indicated that the mechanism of LHQW-XYS in the treatment of olfactory impairment in COVID-19 may be due to the regulation of related signaling pathways, such as Serotonergic synapse and Regulation of lipolysis in adipocytes. Molecular docking showed that six active components (quercetin, luteolin, kaempferol, 7-methoxy-2-methylisoflavone, wogonin, medicarpin) and two key genes (PTGS2, PPARG) had good binding properties. In the end, we conclude that LHQW-XYS may act on Serotonergic synapse and Regulation of lipolysis in adipocyte pathways to achieve anti-COVID-19 olfactory impairment-associated effects.

Key words: LHQWXYS, COVID-19 olfactory impairment-associate, Network pharmacology, Molecular docking

Supporting: