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Validation of the Anticolitis Efficacy of the Jian-Wei-Yu-Yang Formula

BACKGROUND: Inflammatory bowel disease (IBD) is a major cause of morbidity and mortality due to its repetitive remission and relapse. The Jian-Wei-Yu-Yang (JW) formula has a historical application in the clinic to combat gastrointestinal disorders. The investigation aimed to explore the molecular an...

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Autores principales: Yan, Jing, Tang, Yan, Yu, Wei, Jiang, Lu, Liu, Chen, Li, Qi, Zhang, Zhiqiang, Shao, Changlei, Zheng, Yang, Liu, Xihao, Liu, Xincheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9451982/
https://www.ncbi.nlm.nih.gov/pubmed/36091591
http://dx.doi.org/10.1155/2022/9110704
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author Yan, Jing
Tang, Yan
Yu, Wei
Jiang, Lu
Liu, Chen
Li, Qi
Zhang, Zhiqiang
Shao, Changlei
Zheng, Yang
Liu, Xihao
Liu, Xincheng
author_facet Yan, Jing
Tang, Yan
Yu, Wei
Jiang, Lu
Liu, Chen
Li, Qi
Zhang, Zhiqiang
Shao, Changlei
Zheng, Yang
Liu, Xihao
Liu, Xincheng
author_sort Yan, Jing
collection PubMed
description BACKGROUND: Inflammatory bowel disease (IBD) is a major cause of morbidity and mortality due to its repetitive remission and relapse. The Jian-Wei-Yu-Yang (JW) formula has a historical application in the clinic to combat gastrointestinal disorders. The investigation aimed to explore the molecular and cellular mechanisms of JW. METHODS: 2% dextran sodium sulfate (DSS) was diluted in drinking water and given to mice for 5 days to establish murine models of experimental colitis, and different doses of JW solution were administered for 14 days. Network pharmacology analysis and weighted gene co-expression network analysis (WGCNA) were utilized to predict the therapeutic role of JW against experimental colitis and colitis-associated colorectal cancer (CAC). 16S rRNA sequencing and untargeted metabolomics were conducted using murine feces. Western blotting, immunocytochemistry, and wound healing experiments were performed to confirm the molecular mechanisms. RESULTS: (1) Liquid chromatography with mass spectrometry was utilized to confirm the validity of the JW formula. The high dose of JW treatment markedly attenuated DSS-induced experimental colitis progression, and the targets were enriched in inflammation, infection, and tumorigenesis. (2) The JW targets were related to the survival probability in patients with colorectal cancer, underlying a potential therapeutic value in CRC intervention. (3) Moreover, the JW therapy successfully rescued the decreased richness and diversity of microbiota, suppressed the potentially pathogenic phenotype of the gut microorganisms, and increased cytochrome P450 activity in murine colitis models. (4) Our in vitro experiments confirmed that the JW treatment suppressed caspase3-dependent pyroptosis, hypoxia-inducible factor 1α (HIF1α), and interleukin-1b (IL-1b) in the colon; facilitated the alternative activation of macrophages (Mφs); and inhibited tumor necrosis factor-α (TNFα)-induced reactive oxygen species (ROS) level in intestinal organoids (IOs). CONCLUSION: The JW capsule attenuated the progression of murine colitis by a prompt resolution of inflammation and bloody stool and by re-establishing a microbiome profile that favors re-epithelization and prevents carcinogenesis.
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spelling pubmed-94519822022-09-08 Validation of the Anticolitis Efficacy of the Jian-Wei-Yu-Yang Formula Yan, Jing Tang, Yan Yu, Wei Jiang, Lu Liu, Chen Li, Qi Zhang, Zhiqiang Shao, Changlei Zheng, Yang Liu, Xihao Liu, Xincheng Evid Based Complement Alternat Med Research Article BACKGROUND: Inflammatory bowel disease (IBD) is a major cause of morbidity and mortality due to its repetitive remission and relapse. The Jian-Wei-Yu-Yang (JW) formula has a historical application in the clinic to combat gastrointestinal disorders. The investigation aimed to explore the molecular and cellular mechanisms of JW. METHODS: 2% dextran sodium sulfate (DSS) was diluted in drinking water and given to mice for 5 days to establish murine models of experimental colitis, and different doses of JW solution were administered for 14 days. Network pharmacology analysis and weighted gene co-expression network analysis (WGCNA) were utilized to predict the therapeutic role of JW against experimental colitis and colitis-associated colorectal cancer (CAC). 16S rRNA sequencing and untargeted metabolomics were conducted using murine feces. Western blotting, immunocytochemistry, and wound healing experiments were performed to confirm the molecular mechanisms. RESULTS: (1) Liquid chromatography with mass spectrometry was utilized to confirm the validity of the JW formula. The high dose of JW treatment markedly attenuated DSS-induced experimental colitis progression, and the targets were enriched in inflammation, infection, and tumorigenesis. (2) The JW targets were related to the survival probability in patients with colorectal cancer, underlying a potential therapeutic value in CRC intervention. (3) Moreover, the JW therapy successfully rescued the decreased richness and diversity of microbiota, suppressed the potentially pathogenic phenotype of the gut microorganisms, and increased cytochrome P450 activity in murine colitis models. (4) Our in vitro experiments confirmed that the JW treatment suppressed caspase3-dependent pyroptosis, hypoxia-inducible factor 1α (HIF1α), and interleukin-1b (IL-1b) in the colon; facilitated the alternative activation of macrophages (Mφs); and inhibited tumor necrosis factor-α (TNFα)-induced reactive oxygen species (ROS) level in intestinal organoids (IOs). CONCLUSION: The JW capsule attenuated the progression of murine colitis by a prompt resolution of inflammation and bloody stool and by re-establishing a microbiome profile that favors re-epithelization and prevents carcinogenesis. Hindawi 2022-08-31 /pmc/articles/PMC9451982/ /pubmed/36091591 http://dx.doi.org/10.1155/2022/9110704 Text en Copyright © 2022 Jing Yan et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yan, Jing
Tang, Yan
Yu, Wei
Jiang, Lu
Liu, Chen
Li, Qi
Zhang, Zhiqiang
Shao, Changlei
Zheng, Yang
Liu, Xihao
Liu, Xincheng
Validation of the Anticolitis Efficacy of the Jian-Wei-Yu-Yang Formula
title Validation of the Anticolitis Efficacy of the Jian-Wei-Yu-Yang Formula
title_full Validation of the Anticolitis Efficacy of the Jian-Wei-Yu-Yang Formula
title_fullStr Validation of the Anticolitis Efficacy of the Jian-Wei-Yu-Yang Formula
title_full_unstemmed Validation of the Anticolitis Efficacy of the Jian-Wei-Yu-Yang Formula
title_short Validation of the Anticolitis Efficacy of the Jian-Wei-Yu-Yang Formula
title_sort validation of the anticolitis efficacy of the jian-wei-yu-yang formula
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9451982/
https://www.ncbi.nlm.nih.gov/pubmed/36091591
http://dx.doi.org/10.1155/2022/9110704
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