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Jatrorrhizine alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression

BACKGROUND: The natural protoberberine jatrorrhizine (JA) is reported to have several medicinal properties and a significant effect on the gut microbiota of mice. The regulation of gut microbiota is generally known to play an important role in the intestinal mucosal immune response to ulcerative col...

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Autores principales: Zhang, Jia Ling, Zhang, Min Na, Wang, Hong Gang, Yang, Xiao Zhong, Yu, Cheng Gong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587631/
https://www.ncbi.nlm.nih.gov/pubmed/36271438
http://dx.doi.org/10.1186/s13099-022-00514-z
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author Zhang, Jia Ling
Zhang, Min Na
Wang, Hong Gang
Yang, Xiao Zhong
Yu, Cheng Gong
author_facet Zhang, Jia Ling
Zhang, Min Na
Wang, Hong Gang
Yang, Xiao Zhong
Yu, Cheng Gong
author_sort Zhang, Jia Ling
collection PubMed
description BACKGROUND: The natural protoberberine jatrorrhizine (JA) is reported to have several medicinal properties and a significant effect on the gut microbiota of mice. The regulation of gut microbiota is generally known to play an important role in the intestinal mucosal immune response to ulcerative colitis (UC). However, whether JA can be used in the treatment of UC is still unclear. Our study aimed to investigate the underlying therapeutic effects and mechanisms of JA in treating colitis. RESULTS: Compared with the DSS-induced colitis model group, the JA + DSS treated group had more significant improvements in weight loss, disease activity index score, colon length shortening, and pathological inflammation. 16s rRNA sequencing analysis showed that JA treatment protected colitis mice against DSS-induced disturbance of gut microbiota. At the phylum level, reductions in Deferribacteres and Proteobacteria were observed in the JA-treated group; At the genus level, the JA-treated group showed an increased relative abundance of Akkermansia and decreased abundance of Escherichia-Shigella, Desulfovibrio, Mucispirillum, etc. Network pharmacology was then used to screen out five drug-disease target genes (NOS2, ESR1, CALM1, CALM2, CALM3). Transcriptomics analysis further validated that the NOS2 expression was significantly reduced in colon tissue of JA-administered mice compared with DSS control mice. Additionally, analysis of correlation suggested that NOS2 expression was negatively correlated with the relative abundance of AKKermansia and positively correlated with Desulfovibrio, Rikenella. CONCLUSION: JA alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-022-00514-z.
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spelling pubmed-95876312022-10-23 Jatrorrhizine alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression Zhang, Jia Ling Zhang, Min Na Wang, Hong Gang Yang, Xiao Zhong Yu, Cheng Gong Gut Pathog Research BACKGROUND: The natural protoberberine jatrorrhizine (JA) is reported to have several medicinal properties and a significant effect on the gut microbiota of mice. The regulation of gut microbiota is generally known to play an important role in the intestinal mucosal immune response to ulcerative colitis (UC). However, whether JA can be used in the treatment of UC is still unclear. Our study aimed to investigate the underlying therapeutic effects and mechanisms of JA in treating colitis. RESULTS: Compared with the DSS-induced colitis model group, the JA + DSS treated group had more significant improvements in weight loss, disease activity index score, colon length shortening, and pathological inflammation. 16s rRNA sequencing analysis showed that JA treatment protected colitis mice against DSS-induced disturbance of gut microbiota. At the phylum level, reductions in Deferribacteres and Proteobacteria were observed in the JA-treated group; At the genus level, the JA-treated group showed an increased relative abundance of Akkermansia and decreased abundance of Escherichia-Shigella, Desulfovibrio, Mucispirillum, etc. Network pharmacology was then used to screen out five drug-disease target genes (NOS2, ESR1, CALM1, CALM2, CALM3). Transcriptomics analysis further validated that the NOS2 expression was significantly reduced in colon tissue of JA-administered mice compared with DSS control mice. Additionally, analysis of correlation suggested that NOS2 expression was negatively correlated with the relative abundance of AKKermansia and positively correlated with Desulfovibrio, Rikenella. CONCLUSION: JA alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-022-00514-z. BioMed Central 2022-10-21 /pmc/articles/PMC9587631/ /pubmed/36271438 http://dx.doi.org/10.1186/s13099-022-00514-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhang, Jia Ling
Zhang, Min Na
Wang, Hong Gang
Yang, Xiao Zhong
Yu, Cheng Gong
Jatrorrhizine alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression
title Jatrorrhizine alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression
title_full Jatrorrhizine alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression
title_fullStr Jatrorrhizine alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression
title_full_unstemmed Jatrorrhizine alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression
title_short Jatrorrhizine alleviates ulcerative colitis via regulating gut microbiota and NOS2 expression
title_sort jatrorrhizine alleviates ulcerative colitis via regulating gut microbiota and nos2 expression
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587631/
https://www.ncbi.nlm.nih.gov/pubmed/36271438
http://dx.doi.org/10.1186/s13099-022-00514-z
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