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Bacteroides plebeius improves muscle wasting in chronic kidney disease by modulating the gut‐renal muscle axis
Chronic kidney disease (CKD) affects approximately 10% of the global population. Muscle atrophy occurs in patients with almost all types of CKD, and the gut microbiome is closely related to protein consumption during chronic renal failure (CRF). This study investigated the effects of Bacteroides ple...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753468/ https://www.ncbi.nlm.nih.gov/pubmed/36458537 http://dx.doi.org/10.1111/jcmm.17626 |
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author | Pei, Tingting Zhu, Daoqi Yang, Sixia Hu, Rong Wang, Fujing Zhang, Jiaxing Yan, Shihua Ju, Liliang He, Zhuoen Han, Zhongxiao He, Jinyue Yan, Yangtian Wang, Mingqing Xiao, Wei Ma, Yun |
author_facet | Pei, Tingting Zhu, Daoqi Yang, Sixia Hu, Rong Wang, Fujing Zhang, Jiaxing Yan, Shihua Ju, Liliang He, Zhuoen Han, Zhongxiao He, Jinyue Yan, Yangtian Wang, Mingqing Xiao, Wei Ma, Yun |
author_sort | Pei, Tingting |
collection | PubMed |
description | Chronic kidney disease (CKD) affects approximately 10% of the global population. Muscle atrophy occurs in patients with almost all types of CKD, and the gut microbiome is closely related to protein consumption during chronic renal failure (CRF). This study investigated the effects of Bacteroides plebeius on protein energy consumption in rats with CKD, and our results suggest that Bacteroides plebeius may combat muscle atrophy through the Mystn/ActRIIB/SMAD2 pathway. A total of 5/6 Nx rats were used as a model of muscle wasting in CKD. The rats with muscle wasting were administered Bacteroides plebeius (2 × 10(8) cfu/0.2 ml) for 8 weeks. The results showed that Bacteroides plebeius administration significantly inhibited muscle wasting in CKD. High‐throughput 16 S rRNA pyrosequencing revealed that supplementation with Bacteroides plebeius rescued disturbances in the gut microbiota. Bacteroides plebeius could also enhance the barrier function of the intestinal mucosa. Bacteroides plebeius may modulate the gut microbiome and reduce protein consumption by increasing the abundance of probiotics and reducing damage to the intestinal mucosal barrier. Our findings suggest that Bacteroides plebeius may combat muscle atrophy through the Mystn/ActRIIB/SMAD2 pathway. |
format | Online Article Text |
id | pubmed-9753468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97534682022-12-19 Bacteroides plebeius improves muscle wasting in chronic kidney disease by modulating the gut‐renal muscle axis Pei, Tingting Zhu, Daoqi Yang, Sixia Hu, Rong Wang, Fujing Zhang, Jiaxing Yan, Shihua Ju, Liliang He, Zhuoen Han, Zhongxiao He, Jinyue Yan, Yangtian Wang, Mingqing Xiao, Wei Ma, Yun J Cell Mol Med Original Articles Chronic kidney disease (CKD) affects approximately 10% of the global population. Muscle atrophy occurs in patients with almost all types of CKD, and the gut microbiome is closely related to protein consumption during chronic renal failure (CRF). This study investigated the effects of Bacteroides plebeius on protein energy consumption in rats with CKD, and our results suggest that Bacteroides plebeius may combat muscle atrophy through the Mystn/ActRIIB/SMAD2 pathway. A total of 5/6 Nx rats were used as a model of muscle wasting in CKD. The rats with muscle wasting were administered Bacteroides plebeius (2 × 10(8) cfu/0.2 ml) for 8 weeks. The results showed that Bacteroides plebeius administration significantly inhibited muscle wasting in CKD. High‐throughput 16 S rRNA pyrosequencing revealed that supplementation with Bacteroides plebeius rescued disturbances in the gut microbiota. Bacteroides plebeius could also enhance the barrier function of the intestinal mucosa. Bacteroides plebeius may modulate the gut microbiome and reduce protein consumption by increasing the abundance of probiotics and reducing damage to the intestinal mucosal barrier. Our findings suggest that Bacteroides plebeius may combat muscle atrophy through the Mystn/ActRIIB/SMAD2 pathway. John Wiley and Sons Inc. 2022-12-02 2022-12 /pmc/articles/PMC9753468/ /pubmed/36458537 http://dx.doi.org/10.1111/jcmm.17626 Text en © 2022 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Pei, Tingting Zhu, Daoqi Yang, Sixia Hu, Rong Wang, Fujing Zhang, Jiaxing Yan, Shihua Ju, Liliang He, Zhuoen Han, Zhongxiao He, Jinyue Yan, Yangtian Wang, Mingqing Xiao, Wei Ma, Yun Bacteroides plebeius improves muscle wasting in chronic kidney disease by modulating the gut‐renal muscle axis |
title |
Bacteroides plebeius improves muscle wasting in chronic kidney disease by modulating the gut‐renal muscle axis |
title_full |
Bacteroides plebeius improves muscle wasting in chronic kidney disease by modulating the gut‐renal muscle axis |
title_fullStr |
Bacteroides plebeius improves muscle wasting in chronic kidney disease by modulating the gut‐renal muscle axis |
title_full_unstemmed |
Bacteroides plebeius improves muscle wasting in chronic kidney disease by modulating the gut‐renal muscle axis |
title_short |
Bacteroides plebeius improves muscle wasting in chronic kidney disease by modulating the gut‐renal muscle axis |
title_sort | bacteroides plebeius improves muscle wasting in chronic kidney disease by modulating the gut‐renal muscle axis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753468/ https://www.ncbi.nlm.nih.gov/pubmed/36458537 http://dx.doi.org/10.1111/jcmm.17626 |
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