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Rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis
Background: Gut microbiota, which plays a crucial role in inflammatory bowel diseases (IBD), might have therapeutic benefits for ulcerative colitis or Crohn's disease. Targeting gut microbiota represents a new treatment strategy for IBD patients. Rhein is one of the main components of rhubarb a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482825/ https://www.ncbi.nlm.nih.gov/pubmed/32929373 http://dx.doi.org/10.7150/thno.43528 |
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author | Wu, Jiawei Wei, Zhonghong Cheng, Peng Qian, Cheng Xu, Fangming Yang, Yu Wang, Aiyun Chen, Wenxing Sun, Zhiguang Lu, Yin |
author_facet | Wu, Jiawei Wei, Zhonghong Cheng, Peng Qian, Cheng Xu, Fangming Yang, Yu Wang, Aiyun Chen, Wenxing Sun, Zhiguang Lu, Yin |
author_sort | Wu, Jiawei |
collection | PubMed |
description | Background: Gut microbiota, which plays a crucial role in inflammatory bowel diseases (IBD), might have therapeutic benefits for ulcerative colitis or Crohn's disease. Targeting gut microbiota represents a new treatment strategy for IBD patients. Rhein is one of the main components of rhubarb and exhibits poor oral bioavailability but still exerts anti-inflammatory effects in some diseases. Therefore, we investigated the effect of rhein on colitis and studied its possible mechanisms. Methods: The chronic mouse colitis model was induced by four rounds of 2% dextran sulfate sodium (DSS) treatment. The mice were treated with 50 mg/kg and 100 mg/kg rhein daily, body weight, colon length, histological score, inflammatory cytokines in serum or intestine, and fecal lipocalin 2 concentration were determined. Th17 cell, Th1 cell and Th2 cell infiltration in the mesenteric lymph node were analyzed by flow cytometry. Metabolic profiles were collected by non-targeted metabolomics and key metabolic pathways were identified using MetaboAnalyst 4.0. We also assessed intestinal barrier permeability and performed 16s rDNA sequencing. Lactobacillus sp. was cultured, and fecal microbiota transplantation (FMT) was employed to evaluate the contribution of gut microbiota. Results: Rhein could significantly alleviate DSS-induced chronic colitis. Uric acid was identified as a crucial modulator of colitis and rhein treatment led to decreased uric acid levels. We determined that rhein changed purine metabolism indirectly, while the probiotic Lactobacillus was involved in the regulation of host metabolism. Uric acid resulted in a worsened intestinal barrier, which could be rescued by rhein. We further confirmed that rhein-treated gut microbiota was sufficient to relieve DSS-induced colitis by FMT. Conclusion: We showed that rhein could modulate gut microbiota, which indirectly changed purine metabolism in the intestine and subsequently alleviated colitis. Our study has identified a new approach to the clinical treatment of colitis. |
format | Online Article Text |
id | pubmed-7482825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-74828252020-09-13 Rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis Wu, Jiawei Wei, Zhonghong Cheng, Peng Qian, Cheng Xu, Fangming Yang, Yu Wang, Aiyun Chen, Wenxing Sun, Zhiguang Lu, Yin Theranostics Research Paper Background: Gut microbiota, which plays a crucial role in inflammatory bowel diseases (IBD), might have therapeutic benefits for ulcerative colitis or Crohn's disease. Targeting gut microbiota represents a new treatment strategy for IBD patients. Rhein is one of the main components of rhubarb and exhibits poor oral bioavailability but still exerts anti-inflammatory effects in some diseases. Therefore, we investigated the effect of rhein on colitis and studied its possible mechanisms. Methods: The chronic mouse colitis model was induced by four rounds of 2% dextran sulfate sodium (DSS) treatment. The mice were treated with 50 mg/kg and 100 mg/kg rhein daily, body weight, colon length, histological score, inflammatory cytokines in serum or intestine, and fecal lipocalin 2 concentration were determined. Th17 cell, Th1 cell and Th2 cell infiltration in the mesenteric lymph node were analyzed by flow cytometry. Metabolic profiles were collected by non-targeted metabolomics and key metabolic pathways were identified using MetaboAnalyst 4.0. We also assessed intestinal barrier permeability and performed 16s rDNA sequencing. Lactobacillus sp. was cultured, and fecal microbiota transplantation (FMT) was employed to evaluate the contribution of gut microbiota. Results: Rhein could significantly alleviate DSS-induced chronic colitis. Uric acid was identified as a crucial modulator of colitis and rhein treatment led to decreased uric acid levels. We determined that rhein changed purine metabolism indirectly, while the probiotic Lactobacillus was involved in the regulation of host metabolism. Uric acid resulted in a worsened intestinal barrier, which could be rescued by rhein. We further confirmed that rhein-treated gut microbiota was sufficient to relieve DSS-induced colitis by FMT. Conclusion: We showed that rhein could modulate gut microbiota, which indirectly changed purine metabolism in the intestine and subsequently alleviated colitis. Our study has identified a new approach to the clinical treatment of colitis. Ivyspring International Publisher 2020-08-29 /pmc/articles/PMC7482825/ /pubmed/32929373 http://dx.doi.org/10.7150/thno.43528 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Wu, Jiawei Wei, Zhonghong Cheng, Peng Qian, Cheng Xu, Fangming Yang, Yu Wang, Aiyun Chen, Wenxing Sun, Zhiguang Lu, Yin Rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis |
title | Rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis |
title_full | Rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis |
title_fullStr | Rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis |
title_full_unstemmed | Rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis |
title_short | Rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis |
title_sort | rhein modulates host purine metabolism in intestine through gut microbiota and ameliorates experimental colitis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482825/ https://www.ncbi.nlm.nih.gov/pubmed/32929373 http://dx.doi.org/10.7150/thno.43528 |
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