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Lycium barbarum polysaccharide modulates gut microbiota to alleviate rheumatoid arthritis in a rat model

Rheumatoid arthritis (RA) seriously impairs the quality of life of sufferers. It has been shown that Lycium barbarum polysaccharide (LBP), a natural active indigestible ingredient with medicinal and edible functions, can effectively relieve RA, however, whether this effect is related to gut microbio...

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Autores principales: Lai, Wenjia, Wang, Chunyan, Lai, Renfa, Peng, Xichun, Luo, Jianming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304368/
https://www.ncbi.nlm.nih.gov/pubmed/35864275
http://dx.doi.org/10.1038/s41538-022-00149-z
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author Lai, Wenjia
Wang, Chunyan
Lai, Renfa
Peng, Xichun
Luo, Jianming
author_facet Lai, Wenjia
Wang, Chunyan
Lai, Renfa
Peng, Xichun
Luo, Jianming
author_sort Lai, Wenjia
collection PubMed
description Rheumatoid arthritis (RA) seriously impairs the quality of life of sufferers. It has been shown that Lycium barbarum polysaccharide (LBP), a natural active indigestible ingredient with medicinal and edible functions, can effectively relieve RA, however, whether this effect is related to gut microbiota is not known. This study aimed to explore the RA alleviating mechanism of LBP mediated by gut microbiota using a collagen-induced arthritis rat model. The results showed that LBP significantly changed the gut microflora structure accompanied with the RA alleviation. Specifically, a LBP intervention reduced the relative abundance of Lachnospiraceae_NK4A136_group and uncultured_bacterium_f_Ruminococcaceae and significantly increased the abundance of Romboutsia, Lactobacillus, Dubosiella and Faecalibaculum. The mRNA contents of several colonic epithelial genes including Dpep3, Gstm6, Slc27a2, Col11a2, Sycp2, SNORA22, Tnni1, Gpnmb, Mypn and Acsl6, which are potentially associated to RA, were down-regulated due to the DNA hypermethylation, possibly caused by the elevating content of a bacterial metabolite S-adenosyl methionine (SAM). In conclusion, our current study suggests that LBP alleviated RA by reshaping the composition of intestinal microflora which may generate SAM, inducing DNA hypermethylation of RA-related genes in the host intestinal epithelium and subsequently reducing their expression.
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spelling pubmed-93043682022-07-23 Lycium barbarum polysaccharide modulates gut microbiota to alleviate rheumatoid arthritis in a rat model Lai, Wenjia Wang, Chunyan Lai, Renfa Peng, Xichun Luo, Jianming NPJ Sci Food Article Rheumatoid arthritis (RA) seriously impairs the quality of life of sufferers. It has been shown that Lycium barbarum polysaccharide (LBP), a natural active indigestible ingredient with medicinal and edible functions, can effectively relieve RA, however, whether this effect is related to gut microbiota is not known. This study aimed to explore the RA alleviating mechanism of LBP mediated by gut microbiota using a collagen-induced arthritis rat model. The results showed that LBP significantly changed the gut microflora structure accompanied with the RA alleviation. Specifically, a LBP intervention reduced the relative abundance of Lachnospiraceae_NK4A136_group and uncultured_bacterium_f_Ruminococcaceae and significantly increased the abundance of Romboutsia, Lactobacillus, Dubosiella and Faecalibaculum. The mRNA contents of several colonic epithelial genes including Dpep3, Gstm6, Slc27a2, Col11a2, Sycp2, SNORA22, Tnni1, Gpnmb, Mypn and Acsl6, which are potentially associated to RA, were down-regulated due to the DNA hypermethylation, possibly caused by the elevating content of a bacterial metabolite S-adenosyl methionine (SAM). In conclusion, our current study suggests that LBP alleviated RA by reshaping the composition of intestinal microflora which may generate SAM, inducing DNA hypermethylation of RA-related genes in the host intestinal epithelium and subsequently reducing their expression. Nature Publishing Group UK 2022-07-21 /pmc/articles/PMC9304368/ /pubmed/35864275 http://dx.doi.org/10.1038/s41538-022-00149-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lai, Wenjia
Wang, Chunyan
Lai, Renfa
Peng, Xichun
Luo, Jianming
Lycium barbarum polysaccharide modulates gut microbiota to alleviate rheumatoid arthritis in a rat model
title Lycium barbarum polysaccharide modulates gut microbiota to alleviate rheumatoid arthritis in a rat model
title_full Lycium barbarum polysaccharide modulates gut microbiota to alleviate rheumatoid arthritis in a rat model
title_fullStr Lycium barbarum polysaccharide modulates gut microbiota to alleviate rheumatoid arthritis in a rat model
title_full_unstemmed Lycium barbarum polysaccharide modulates gut microbiota to alleviate rheumatoid arthritis in a rat model
title_short Lycium barbarum polysaccharide modulates gut microbiota to alleviate rheumatoid arthritis in a rat model
title_sort lycium barbarum polysaccharide modulates gut microbiota to alleviate rheumatoid arthritis in a rat model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304368/
https://www.ncbi.nlm.nih.gov/pubmed/35864275
http://dx.doi.org/10.1038/s41538-022-00149-z
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