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Study on the protective effect of berberine treatment on sepsis based on gut microbiota and metabolomic analysis

INTRODUCTION: Sepsis, an infection with multiorgan dysfunction, is a serious burden on human health. Berberine (BBR), a bioactive component, has a protective effect on sepsis and the effect may be related to gut microbiota. However, studies on the role of BBR with gut microbiota in sepsis are lackin...

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Autores principales: Pan, Huibin, Huo, Lixia, Shen, Weiyun, Dai, Zhuquan, Bao, Ying, Ji, Chaohui, Zhang, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806126/
https://www.ncbi.nlm.nih.gov/pubmed/36601077
http://dx.doi.org/10.3389/fnut.2022.1049106
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author Pan, Huibin
Huo, Lixia
Shen, Weiyun
Dai, Zhuquan
Bao, Ying
Ji, Chaohui
Zhang, Jie
author_facet Pan, Huibin
Huo, Lixia
Shen, Weiyun
Dai, Zhuquan
Bao, Ying
Ji, Chaohui
Zhang, Jie
author_sort Pan, Huibin
collection PubMed
description INTRODUCTION: Sepsis, an infection with multiorgan dysfunction, is a serious burden on human health. Berberine (BBR), a bioactive component, has a protective effect on sepsis and the effect may be related to gut microbiota. However, studies on the role of BBR with gut microbiota in sepsis are lacking. Therefore, this study investigated the ameliorative effects and the underlying mechanisms of BBR on cecal ligature and puncture (CLP) rats. METHODS: This study has observed the effect of BBR on pathological injury, Inflammation, intestinal barrier function, gut microbiota, and metabolite change in CLP rats by Hematoxylin-eosin staining, enzyme-linked immunosorbent assays, flow cytometry, 16S rDNA, and metabolomics analyses. RESULTS: The inhibition effects of BBR treatment on the histological damage of the lung, kidney, and ileum, the interleukin (IL)-1b, IL-6, IL-17A, and monocyte chemokine-1 levels in serum in CLP rats were proved. Also, the BBR inhibited the diamine-oxidase and fluorescein isothiocyanate-dextran 40 levels, suggesting it can improve intestinal barrier function disorders. The cluster of differentiation (CD) 4(+), CD8(+), and CD25(+) Forkhead box protein P3 (Foxp3) + T lymphocytes in splenocytes were up-regulated by BBR, while the IL-17A+CD4+ cell level was decreased. The abundance of gut microbiota in CLP rats was significantly different from that of the sham and BBR treatment rats. The significantly changed metabolites in the serum mainly included carbohydrates, phenols, benzoic acids, alcohols, vitamins et al. Additionally, this study predicted that the biological mechanism of BBR to ameliorate sepsis involves glycolysis-, nucleotide-, and amino acid-related metabolic pathways. DISCUSSION: This study proved the strong correlation between the improvement effect of BBR on sepsis and gut microbiota and analyzed by metabolomics that gut microbiota may improve CLP rats through metabolites, providing a scientific basis for BBR to improve sepsis and a new direction for the study of the biological mechanism.
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spelling pubmed-98061262023-01-03 Study on the protective effect of berberine treatment on sepsis based on gut microbiota and metabolomic analysis Pan, Huibin Huo, Lixia Shen, Weiyun Dai, Zhuquan Bao, Ying Ji, Chaohui Zhang, Jie Front Nutr Nutrition INTRODUCTION: Sepsis, an infection with multiorgan dysfunction, is a serious burden on human health. Berberine (BBR), a bioactive component, has a protective effect on sepsis and the effect may be related to gut microbiota. However, studies on the role of BBR with gut microbiota in sepsis are lacking. Therefore, this study investigated the ameliorative effects and the underlying mechanisms of BBR on cecal ligature and puncture (CLP) rats. METHODS: This study has observed the effect of BBR on pathological injury, Inflammation, intestinal barrier function, gut microbiota, and metabolite change in CLP rats by Hematoxylin-eosin staining, enzyme-linked immunosorbent assays, flow cytometry, 16S rDNA, and metabolomics analyses. RESULTS: The inhibition effects of BBR treatment on the histological damage of the lung, kidney, and ileum, the interleukin (IL)-1b, IL-6, IL-17A, and monocyte chemokine-1 levels in serum in CLP rats were proved. Also, the BBR inhibited the diamine-oxidase and fluorescein isothiocyanate-dextran 40 levels, suggesting it can improve intestinal barrier function disorders. The cluster of differentiation (CD) 4(+), CD8(+), and CD25(+) Forkhead box protein P3 (Foxp3) + T lymphocytes in splenocytes were up-regulated by BBR, while the IL-17A+CD4+ cell level was decreased. The abundance of gut microbiota in CLP rats was significantly different from that of the sham and BBR treatment rats. The significantly changed metabolites in the serum mainly included carbohydrates, phenols, benzoic acids, alcohols, vitamins et al. Additionally, this study predicted that the biological mechanism of BBR to ameliorate sepsis involves glycolysis-, nucleotide-, and amino acid-related metabolic pathways. DISCUSSION: This study proved the strong correlation between the improvement effect of BBR on sepsis and gut microbiota and analyzed by metabolomics that gut microbiota may improve CLP rats through metabolites, providing a scientific basis for BBR to improve sepsis and a new direction for the study of the biological mechanism. Frontiers Media S.A. 2022-12-19 /pmc/articles/PMC9806126/ /pubmed/36601077 http://dx.doi.org/10.3389/fnut.2022.1049106 Text en Copyright © 2022 Pan, Huo, Shen, Dai, Bao, Ji and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Pan, Huibin
Huo, Lixia
Shen, Weiyun
Dai, Zhuquan
Bao, Ying
Ji, Chaohui
Zhang, Jie
Study on the protective effect of berberine treatment on sepsis based on gut microbiota and metabolomic analysis
title Study on the protective effect of berberine treatment on sepsis based on gut microbiota and metabolomic analysis
title_full Study on the protective effect of berberine treatment on sepsis based on gut microbiota and metabolomic analysis
title_fullStr Study on the protective effect of berberine treatment on sepsis based on gut microbiota and metabolomic analysis
title_full_unstemmed Study on the protective effect of berberine treatment on sepsis based on gut microbiota and metabolomic analysis
title_short Study on the protective effect of berberine treatment on sepsis based on gut microbiota and metabolomic analysis
title_sort study on the protective effect of berberine treatment on sepsis based on gut microbiota and metabolomic analysis
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806126/
https://www.ncbi.nlm.nih.gov/pubmed/36601077
http://dx.doi.org/10.3389/fnut.2022.1049106
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