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Bifidobacterium longum R0175 Protects Rats against d-Galactosamine-Induced Acute Liver Failure

Acute liver failure is a severe liver disorder that poses considerable global challenges. Previous studies on Bifidobacterium longum R0175 have mainly focused on its psychotropic functions. The current research focused on the protective efficacy of B. longum R0175 against acute liver failure caused...

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Autores principales: Wang, Kaicen, Lv, Longxian, Yan, Ren, Wang, Qiangqiang, Jiang, Huiyong, Wu, Wenrui, Li, Yating, Ye, Jianzhong, Wu, Jingjing, Yang, Liya, Bian, Xiaoyuan, Jiang, Xianwan, Lu, Yanmeng, Xie, Jiaojiao, Wang, Qing, Shen, Jian, Li, Lanjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992372/
https://www.ncbi.nlm.nih.gov/pubmed/31996423
http://dx.doi.org/10.1128/mSphere.00791-19
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author Wang, Kaicen
Lv, Longxian
Yan, Ren
Wang, Qiangqiang
Jiang, Huiyong
Wu, Wenrui
Li, Yating
Ye, Jianzhong
Wu, Jingjing
Yang, Liya
Bian, Xiaoyuan
Jiang, Xianwan
Lu, Yanmeng
Xie, Jiaojiao
Wang, Qing
Shen, Jian
Li, Lanjuan
author_facet Wang, Kaicen
Lv, Longxian
Yan, Ren
Wang, Qiangqiang
Jiang, Huiyong
Wu, Wenrui
Li, Yating
Ye, Jianzhong
Wu, Jingjing
Yang, Liya
Bian, Xiaoyuan
Jiang, Xianwan
Lu, Yanmeng
Xie, Jiaojiao
Wang, Qing
Shen, Jian
Li, Lanjuan
author_sort Wang, Kaicen
collection PubMed
description Acute liver failure is a severe liver disorder that poses considerable global challenges. Previous studies on Bifidobacterium longum R0175 have mainly focused on its psychotropic functions. The current research focused on the protective efficacy of B. longum R0175 against acute liver failure caused by d-galactosamine (d-GalN) in rats and further tested the hypothesis that B. longum R0175 exerted liver-protective effects by affecting the intestinal microbiota and fecal metabolites and by inhibiting inflammation. We found that oral gavage of B. longum R0175 markedly reduced the severity of liver injury in d-GalN-treated rats, as evidenced by decreased serum levels of aspartate aminotransferase (AST) and total bile acids (TBAs) (P < 0.05). Moreover, the plasma concentrations of proinflammatory cytokines (interleukin 1β [IL-1β] and tumor necrosis factor-α [TNF-α]) and chemokines (granulocyte-macrophage colony-stimulating factor [GM-CSF], macrophage chemoattractant protein 1 [MCP-1], chemokine [C-X-C motif] ligand 1 [CXCL1], chemokine [C-C motif] ligand 5 [CCL5], and macrophage inflammatory protein-1α [MIP-1α]) were also markedly reduced (P < 0.05). Pretreatment with B. longum R0175 partially reversed the gut microbiota dysbiosis in rats with liver injury by increasing the relative abundances of potentially beneficial bacteria, such as Alloprevotella spp., and decreasing the relative abundances of potentially harmful bacteria, such as Acetatifactor muris, Butyricimonas spp., and Oscillibacter spp. Furthermore, B. longum R0175 administration partially improved the metabolic function of the intestinal microbes, as indicated by the decreased level of lithocholic acid found in the feces. IMPORTANCE Our research investigated the protective and preventive roles of B. longum R0175 in a rat model of acute liver failure. The results illustrated that this probiotic strain exhibited protective effects in rats with acute liver failure. Thus, B. longum R0175 showed clinical application prospects that required further exploration.
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spelling pubmed-69923722020-02-04 Bifidobacterium longum R0175 Protects Rats against d-Galactosamine-Induced Acute Liver Failure Wang, Kaicen Lv, Longxian Yan, Ren Wang, Qiangqiang Jiang, Huiyong Wu, Wenrui Li, Yating Ye, Jianzhong Wu, Jingjing Yang, Liya Bian, Xiaoyuan Jiang, Xianwan Lu, Yanmeng Xie, Jiaojiao Wang, Qing Shen, Jian Li, Lanjuan mSphere Research Article Acute liver failure is a severe liver disorder that poses considerable global challenges. Previous studies on Bifidobacterium longum R0175 have mainly focused on its psychotropic functions. The current research focused on the protective efficacy of B. longum R0175 against acute liver failure caused by d-galactosamine (d-GalN) in rats and further tested the hypothesis that B. longum R0175 exerted liver-protective effects by affecting the intestinal microbiota and fecal metabolites and by inhibiting inflammation. We found that oral gavage of B. longum R0175 markedly reduced the severity of liver injury in d-GalN-treated rats, as evidenced by decreased serum levels of aspartate aminotransferase (AST) and total bile acids (TBAs) (P < 0.05). Moreover, the plasma concentrations of proinflammatory cytokines (interleukin 1β [IL-1β] and tumor necrosis factor-α [TNF-α]) and chemokines (granulocyte-macrophage colony-stimulating factor [GM-CSF], macrophage chemoattractant protein 1 [MCP-1], chemokine [C-X-C motif] ligand 1 [CXCL1], chemokine [C-C motif] ligand 5 [CCL5], and macrophage inflammatory protein-1α [MIP-1α]) were also markedly reduced (P < 0.05). Pretreatment with B. longum R0175 partially reversed the gut microbiota dysbiosis in rats with liver injury by increasing the relative abundances of potentially beneficial bacteria, such as Alloprevotella spp., and decreasing the relative abundances of potentially harmful bacteria, such as Acetatifactor muris, Butyricimonas spp., and Oscillibacter spp. Furthermore, B. longum R0175 administration partially improved the metabolic function of the intestinal microbes, as indicated by the decreased level of lithocholic acid found in the feces. IMPORTANCE Our research investigated the protective and preventive roles of B. longum R0175 in a rat model of acute liver failure. The results illustrated that this probiotic strain exhibited protective effects in rats with acute liver failure. Thus, B. longum R0175 showed clinical application prospects that required further exploration. American Society for Microbiology 2020-01-29 /pmc/articles/PMC6992372/ /pubmed/31996423 http://dx.doi.org/10.1128/mSphere.00791-19 Text en Copyright © 2020 Wang et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Wang, Kaicen
Lv, Longxian
Yan, Ren
Wang, Qiangqiang
Jiang, Huiyong
Wu, Wenrui
Li, Yating
Ye, Jianzhong
Wu, Jingjing
Yang, Liya
Bian, Xiaoyuan
Jiang, Xianwan
Lu, Yanmeng
Xie, Jiaojiao
Wang, Qing
Shen, Jian
Li, Lanjuan
Bifidobacterium longum R0175 Protects Rats against d-Galactosamine-Induced Acute Liver Failure
title Bifidobacterium longum R0175 Protects Rats against d-Galactosamine-Induced Acute Liver Failure
title_full Bifidobacterium longum R0175 Protects Rats against d-Galactosamine-Induced Acute Liver Failure
title_fullStr Bifidobacterium longum R0175 Protects Rats against d-Galactosamine-Induced Acute Liver Failure
title_full_unstemmed Bifidobacterium longum R0175 Protects Rats against d-Galactosamine-Induced Acute Liver Failure
title_short Bifidobacterium longum R0175 Protects Rats against d-Galactosamine-Induced Acute Liver Failure
title_sort bifidobacterium longum r0175 protects rats against d-galactosamine-induced acute liver failure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992372/
https://www.ncbi.nlm.nih.gov/pubmed/31996423
http://dx.doi.org/10.1128/mSphere.00791-19
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