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Blueberry Attenuates Liver Fibrosis, Protects Intestinal Epithelial Barrier, and Maintains Gut Microbiota Homeostasis

OBJECTIVE: Recently, blueberry has been identified as a candidate for the treatment of liver fibrosis. Given the role of gut-liver axis in liver fibrosis and the importance of the gut microbiota homeostasis to the maintenance of the intestinal epithelial barrier, this study aimed to investigate whet...

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Autores principales: Yan, Zhiqiang, Yang, Fang, Hong, Zhu, Wang, Shishun, Jinjuan, Zhang, Han, Bing, Xie, Rujia, Leng, Feiyun, Yang, Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893245/
https://www.ncbi.nlm.nih.gov/pubmed/31886154
http://dx.doi.org/10.1155/2019/5236149
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author Yan, Zhiqiang
Yang, Fang
Hong, Zhu
Wang, Shishun
Jinjuan, Zhang
Han, Bing
Xie, Rujia
Leng, Feiyun
Yang, Qin
author_facet Yan, Zhiqiang
Yang, Fang
Hong, Zhu
Wang, Shishun
Jinjuan, Zhang
Han, Bing
Xie, Rujia
Leng, Feiyun
Yang, Qin
author_sort Yan, Zhiqiang
collection PubMed
description OBJECTIVE: Recently, blueberry has been identified as a candidate for the treatment of liver fibrosis. Given the role of gut-liver axis in liver fibrosis and the importance of the gut microbiota homeostasis to the maintenance of the intestinal epithelial barrier, this study aimed to investigate whether blueberry could attenuate liver fibrosis and protect the intestinal epithelial barrier by maintaining the homeostasis of the gut microbiota. METHOD: A CCl(4)-induced rat liver fibrosis model was used to detect the roles of blueberry in liver fibrosis and intestinal epithelial barrier. The liver weight and body weight were measured, the liver function was monitored by ALT and AST activity, protein and mRNA were determined by western blot and RT-qPCR, and the gut microbiome was detected by Miseq. RESULTS: The results showed that blueberry could reduce the rate of liver weight/body weight gain (p < 0.05), ALT (p < 0.01) and AST (p < 0.05) activity, and the expression of collagen I (p < 0.01), collagen IV (p < 0.01), and α-SMA (p < 0.01) expression in CCl(4)-induced rat liver. CCl(4) impaired the intestinal epithelial barrier and decreased the expression of the tight junction protein. Blueberry restored the intestinal epithelial barrier and increased the expression of the tight junction protein. The gut microbiota homeostasis was impaired by CCl(4), but after treatment with blueberry, the intestinal flora returned to normal. CONCLUSION: Blueberry attenuated liver fibrosis, protected intestinal epithelial barrier, and maintained the homeostasis of the gut microbiota in a CCl(4)-induced injury rat model.
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spelling pubmed-68932452019-12-29 Blueberry Attenuates Liver Fibrosis, Protects Intestinal Epithelial Barrier, and Maintains Gut Microbiota Homeostasis Yan, Zhiqiang Yang, Fang Hong, Zhu Wang, Shishun Jinjuan, Zhang Han, Bing Xie, Rujia Leng, Feiyun Yang, Qin Can J Gastroenterol Hepatol Research Article OBJECTIVE: Recently, blueberry has been identified as a candidate for the treatment of liver fibrosis. Given the role of gut-liver axis in liver fibrosis and the importance of the gut microbiota homeostasis to the maintenance of the intestinal epithelial barrier, this study aimed to investigate whether blueberry could attenuate liver fibrosis and protect the intestinal epithelial barrier by maintaining the homeostasis of the gut microbiota. METHOD: A CCl(4)-induced rat liver fibrosis model was used to detect the roles of blueberry in liver fibrosis and intestinal epithelial barrier. The liver weight and body weight were measured, the liver function was monitored by ALT and AST activity, protein and mRNA were determined by western blot and RT-qPCR, and the gut microbiome was detected by Miseq. RESULTS: The results showed that blueberry could reduce the rate of liver weight/body weight gain (p < 0.05), ALT (p < 0.01) and AST (p < 0.05) activity, and the expression of collagen I (p < 0.01), collagen IV (p < 0.01), and α-SMA (p < 0.01) expression in CCl(4)-induced rat liver. CCl(4) impaired the intestinal epithelial barrier and decreased the expression of the tight junction protein. Blueberry restored the intestinal epithelial barrier and increased the expression of the tight junction protein. The gut microbiota homeostasis was impaired by CCl(4), but after treatment with blueberry, the intestinal flora returned to normal. CONCLUSION: Blueberry attenuated liver fibrosis, protected intestinal epithelial barrier, and maintained the homeostasis of the gut microbiota in a CCl(4)-induced injury rat model. Hindawi 2019-11-22 /pmc/articles/PMC6893245/ /pubmed/31886154 http://dx.doi.org/10.1155/2019/5236149 Text en Copyright © 2019 Zhiqiang Yan et al. http://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, Zhiqiang
Yang, Fang
Hong, Zhu
Wang, Shishun
Jinjuan, Zhang
Han, Bing
Xie, Rujia
Leng, Feiyun
Yang, Qin
Blueberry Attenuates Liver Fibrosis, Protects Intestinal Epithelial Barrier, and Maintains Gut Microbiota Homeostasis
title Blueberry Attenuates Liver Fibrosis, Protects Intestinal Epithelial Barrier, and Maintains Gut Microbiota Homeostasis
title_full Blueberry Attenuates Liver Fibrosis, Protects Intestinal Epithelial Barrier, and Maintains Gut Microbiota Homeostasis
title_fullStr Blueberry Attenuates Liver Fibrosis, Protects Intestinal Epithelial Barrier, and Maintains Gut Microbiota Homeostasis
title_full_unstemmed Blueberry Attenuates Liver Fibrosis, Protects Intestinal Epithelial Barrier, and Maintains Gut Microbiota Homeostasis
title_short Blueberry Attenuates Liver Fibrosis, Protects Intestinal Epithelial Barrier, and Maintains Gut Microbiota Homeostasis
title_sort blueberry attenuates liver fibrosis, protects intestinal epithelial barrier, and maintains gut microbiota homeostasis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893245/
https://www.ncbi.nlm.nih.gov/pubmed/31886154
http://dx.doi.org/10.1155/2019/5236149
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