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Network pharmacology analysis and experimental study strategy reveals the potential mechanism of puerarin against rotavirus

BACKGROUND: This study aimed to explore the underlying mechanism of puerarin against rotavirus (RV), based on network pharmacology analysis and experimental study in vitro. METHODS: The cytopathic effect inhibition assay with different concentrations of puerarin at different times of infection in vi...

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Autores principales: Chen, Ting, Lin, Yujie, Cao, Zhiqun, Xue, Ye, Wang, Wei, Wang, Xiaoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825547/
https://www.ncbi.nlm.nih.gov/pubmed/35242859
http://dx.doi.org/10.21037/atm-21-6089
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author Chen, Ting
Lin, Yujie
Cao, Zhiqun
Xue, Ye
Wang, Wei
Wang, Xiaoyan
author_facet Chen, Ting
Lin, Yujie
Cao, Zhiqun
Xue, Ye
Wang, Wei
Wang, Xiaoyan
author_sort Chen, Ting
collection PubMed
description BACKGROUND: This study aimed to explore the underlying mechanism of puerarin against rotavirus (RV), based on network pharmacology analysis and experimental study in vitro. METHODS: The cytopathic effect inhibition assay with different concentrations of puerarin at different times of infection in vitro was applied to evaluate the effect of puerarin against human RV G1P[8] Wa strain (HRV Wa). Subsequently, the potential targets of puerarin and RV-related genes were obtained from online databases. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses of the major target genes were also performed. Furthermore, the major targets and signaling pathway related to RV infection were verified at the molecular level via Western blot, quantitative real-time reverse transcription PCR (RT-qPCR), and Enzyme-linked immunosorbent assay (ELISA) tests. RESULTS: Our results suggest that puerarin had a certain inhibitory effect on viral replication and proliferation. The network pharmacology analysis showed that a total of 436 puerarin corresponding target and 497 RV-related targets were acquired from the online databases. The core targets of puerarin against RV, such as Toll-like receptor 4 (TLR4), tumor necrosis factor (TNF), and caspase 3 (CASP3), were identified from the protein-protein interaction (PPI) network. The KEGG analysis indicated that the TLR signaling pathway was one of the crucial mechanisms of puerarin against RV. In particular, puerarin could inhibit the expression of key factors of the TLR4/nuclear factor kappa-B (NF-κB) signaling pathway in HRV-infected Caco-2 cells and regulate the levels of cellular inflammatory factors. CONCLUSIONS: Based on the network pharmacology analysis and experimental study, the study showed that puerarin not only had an anti-RV effect, but could also modulate the inflammatory response induced by RV infection via the TLR4/NF-κB signaling pathway. This study reveals the potential of puerarin in the treatment of RV infection, suggesting that it might be a promising therapeutic agent.
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spelling pubmed-88255472022-03-02 Network pharmacology analysis and experimental study strategy reveals the potential mechanism of puerarin against rotavirus Chen, Ting Lin, Yujie Cao, Zhiqun Xue, Ye Wang, Wei Wang, Xiaoyan Ann Transl Med Original Article BACKGROUND: This study aimed to explore the underlying mechanism of puerarin against rotavirus (RV), based on network pharmacology analysis and experimental study in vitro. METHODS: The cytopathic effect inhibition assay with different concentrations of puerarin at different times of infection in vitro was applied to evaluate the effect of puerarin against human RV G1P[8] Wa strain (HRV Wa). Subsequently, the potential targets of puerarin and RV-related genes were obtained from online databases. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses of the major target genes were also performed. Furthermore, the major targets and signaling pathway related to RV infection were verified at the molecular level via Western blot, quantitative real-time reverse transcription PCR (RT-qPCR), and Enzyme-linked immunosorbent assay (ELISA) tests. RESULTS: Our results suggest that puerarin had a certain inhibitory effect on viral replication and proliferation. The network pharmacology analysis showed that a total of 436 puerarin corresponding target and 497 RV-related targets were acquired from the online databases. The core targets of puerarin against RV, such as Toll-like receptor 4 (TLR4), tumor necrosis factor (TNF), and caspase 3 (CASP3), were identified from the protein-protein interaction (PPI) network. The KEGG analysis indicated that the TLR signaling pathway was one of the crucial mechanisms of puerarin against RV. In particular, puerarin could inhibit the expression of key factors of the TLR4/nuclear factor kappa-B (NF-κB) signaling pathway in HRV-infected Caco-2 cells and regulate the levels of cellular inflammatory factors. CONCLUSIONS: Based on the network pharmacology analysis and experimental study, the study showed that puerarin not only had an anti-RV effect, but could also modulate the inflammatory response induced by RV infection via the TLR4/NF-κB signaling pathway. This study reveals the potential of puerarin in the treatment of RV infection, suggesting that it might be a promising therapeutic agent. AME Publishing Company 2022-01 /pmc/articles/PMC8825547/ /pubmed/35242859 http://dx.doi.org/10.21037/atm-21-6089 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Chen, Ting
Lin, Yujie
Cao, Zhiqun
Xue, Ye
Wang, Wei
Wang, Xiaoyan
Network pharmacology analysis and experimental study strategy reveals the potential mechanism of puerarin against rotavirus
title Network pharmacology analysis and experimental study strategy reveals the potential mechanism of puerarin against rotavirus
title_full Network pharmacology analysis and experimental study strategy reveals the potential mechanism of puerarin against rotavirus
title_fullStr Network pharmacology analysis and experimental study strategy reveals the potential mechanism of puerarin against rotavirus
title_full_unstemmed Network pharmacology analysis and experimental study strategy reveals the potential mechanism of puerarin against rotavirus
title_short Network pharmacology analysis and experimental study strategy reveals the potential mechanism of puerarin against rotavirus
title_sort network pharmacology analysis and experimental study strategy reveals the potential mechanism of puerarin against rotavirus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825547/
https://www.ncbi.nlm.nih.gov/pubmed/35242859
http://dx.doi.org/10.21037/atm-21-6089
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