Resveratrol alleviates DSS-induced IBD in mice by regulating the intestinal microbiota-macrophage-arginine metabolism axis

Abstract Background Inflammatory bowel disease (IBD) is a global disease with a growing public health concern and is associated with a complex interplay of factors, including the microbiota and immune system. Resveratrol, a natural anti-inflammatory and antioxidant agent, is known to relieve IBD but...

Full description

Bibliographic Details
Main Authors: Xinwei Xu, Dickson Kofi Wiredu Ocansey, Bing Pei, Yaqin Zhang, Naijian Wang, Zengxu Wang, Fei Mao
Format: Article
Language:English
Published: BMC 2023-09-01
Series:European Journal of Medical Research
Subjects:
Online Access:https://doi.org/10.1186/s40001-023-01257-6
_version_ 1797577328068395008
author Xinwei Xu
Dickson Kofi Wiredu Ocansey
Bing Pei
Yaqin Zhang
Naijian Wang
Zengxu Wang
Fei Mao
author_facet Xinwei Xu
Dickson Kofi Wiredu Ocansey
Bing Pei
Yaqin Zhang
Naijian Wang
Zengxu Wang
Fei Mao
author_sort Xinwei Xu
collection DOAJ
description Abstract Background Inflammatory bowel disease (IBD) is a global disease with a growing public health concern and is associated with a complex interplay of factors, including the microbiota and immune system. Resveratrol, a natural anti-inflammatory and antioxidant agent, is known to relieve IBD but the mechanism involved is largely unexplored. Methods This study examines the modulatory effect of resveratrol on intestinal immunity, microbiota, metabolites, and related functions and pathways in the BALB/c mice model of IBD. Mouse RAW264.7 macrophage cell line was used to further explore the involvement of the macrophage-arginine metabolism axis. The treatment outcome was assessed through qRT-PCR, western blot, immunofluorescence, immunohistochemistry, and fecal 16S rDNA sequencing and UHPLC/Q-TOF–MS. Results Results showed that resveratrol treatment significantly reduced disease activity index (DAI), retained mice weight, repaired colon and spleen tissues, upregulated IL-10 and the tight junction proteins Occludin and Claudin 1, and decreased pro-inflammatory cytokines IL-1β, IL-6, and TNF-α. Resveratrol reduced the number of dysregulated metabolites and improved the gut microbial community structure and diversity, including reversing changes in the phyla Bacteroidetes, Proteobacteria, and Firmicutes, increasing ‘beneficial’ genera, and decreasing potential pathogens such as Lachnoclostridium, Acinobacter, and Serratia. Arginine–proline metabolism was significantly different between the colitis-treated and untreated groups. In the colon mucosa and RAW264.7 macrophage, resveratrol regulated arginine metabolism towards colon protection by increasing Arg1 and Slc6a8 and decreasing iNOS. Conclusion This uncovers a previously unknown mechanism of resveratrol treatment in IBD and provides the microbiota-macrophage-arginine metabolism axis as a potential therapeutic target for intestinal inflammation.
first_indexed 2024-03-10T22:06:42Z
format Article
id doaj.art-c20cc5c09c844ff3a123e3643a9281f4
institution Directory Open Access Journal
issn 2047-783X
language English
last_indexed 2024-03-10T22:06:42Z
publishDate 2023-09-01
publisher BMC
record_format Article
series European Journal of Medical Research
spelling doaj.art-c20cc5c09c844ff3a123e3643a9281f42023-11-19T12:47:01ZengBMCEuropean Journal of Medical Research2047-783X2023-09-0128111810.1186/s40001-023-01257-6Resveratrol alleviates DSS-induced IBD in mice by regulating the intestinal microbiota-macrophage-arginine metabolism axisXinwei Xu0Dickson Kofi Wiredu Ocansey1Bing Pei2Yaqin Zhang3Naijian Wang4Zengxu Wang5Fei Mao6Key Laboratory of Medical Science and Laboratory Medicine of Jiangsu Province, School of Medicine, Jiangsu UniversityKey Laboratory of Medical Science and Laboratory Medicine of Jiangsu Province, School of Medicine, Jiangsu UniversityThe Affiliated Suqian First People’s Hospital of Nanjing Medical UniversityKey Laboratory of Medical Science and Laboratory Medicine of Jiangsu Province, School of Medicine, Jiangsu UniversityKey Laboratory of Medical Science and Laboratory Medicine of Jiangsu Province, School of Medicine, Jiangsu UniversityZhenjiang Hospital of Chinese Traditional And Western MedicineKey Laboratory of Medical Science and Laboratory Medicine of Jiangsu Province, School of Medicine, Jiangsu UniversityAbstract Background Inflammatory bowel disease (IBD) is a global disease with a growing public health concern and is associated with a complex interplay of factors, including the microbiota and immune system. Resveratrol, a natural anti-inflammatory and antioxidant agent, is known to relieve IBD but the mechanism involved is largely unexplored. Methods This study examines the modulatory effect of resveratrol on intestinal immunity, microbiota, metabolites, and related functions and pathways in the BALB/c mice model of IBD. Mouse RAW264.7 macrophage cell line was used to further explore the involvement of the macrophage-arginine metabolism axis. The treatment outcome was assessed through qRT-PCR, western blot, immunofluorescence, immunohistochemistry, and fecal 16S rDNA sequencing and UHPLC/Q-TOF–MS. Results Results showed that resveratrol treatment significantly reduced disease activity index (DAI), retained mice weight, repaired colon and spleen tissues, upregulated IL-10 and the tight junction proteins Occludin and Claudin 1, and decreased pro-inflammatory cytokines IL-1β, IL-6, and TNF-α. Resveratrol reduced the number of dysregulated metabolites and improved the gut microbial community structure and diversity, including reversing changes in the phyla Bacteroidetes, Proteobacteria, and Firmicutes, increasing ‘beneficial’ genera, and decreasing potential pathogens such as Lachnoclostridium, Acinobacter, and Serratia. Arginine–proline metabolism was significantly different between the colitis-treated and untreated groups. In the colon mucosa and RAW264.7 macrophage, resveratrol regulated arginine metabolism towards colon protection by increasing Arg1 and Slc6a8 and decreasing iNOS. Conclusion This uncovers a previously unknown mechanism of resveratrol treatment in IBD and provides the microbiota-macrophage-arginine metabolism axis as a potential therapeutic target for intestinal inflammation.https://doi.org/10.1186/s40001-023-01257-6Inflammatory bowel diseaseResveratrolMicrobiotaArginine metabolismMacrophage
spellingShingle Xinwei Xu
Dickson Kofi Wiredu Ocansey
Bing Pei
Yaqin Zhang
Naijian Wang
Zengxu Wang
Fei Mao
Resveratrol alleviates DSS-induced IBD in mice by regulating the intestinal microbiota-macrophage-arginine metabolism axis
European Journal of Medical Research
Inflammatory bowel disease
Resveratrol
Microbiota
Arginine metabolism
Macrophage
title Resveratrol alleviates DSS-induced IBD in mice by regulating the intestinal microbiota-macrophage-arginine metabolism axis
title_full Resveratrol alleviates DSS-induced IBD in mice by regulating the intestinal microbiota-macrophage-arginine metabolism axis
title_fullStr Resveratrol alleviates DSS-induced IBD in mice by regulating the intestinal microbiota-macrophage-arginine metabolism axis
title_full_unstemmed Resveratrol alleviates DSS-induced IBD in mice by regulating the intestinal microbiota-macrophage-arginine metabolism axis
title_short Resveratrol alleviates DSS-induced IBD in mice by regulating the intestinal microbiota-macrophage-arginine metabolism axis
title_sort resveratrol alleviates dss induced ibd in mice by regulating the intestinal microbiota macrophage arginine metabolism axis
topic Inflammatory bowel disease
Resveratrol
Microbiota
Arginine metabolism
Macrophage
url https://doi.org/10.1186/s40001-023-01257-6
work_keys_str_mv AT xinweixu resveratrolalleviatesdssinducedibdinmicebyregulatingtheintestinalmicrobiotamacrophageargininemetabolismaxis
AT dicksonkofiwireduocansey resveratrolalleviatesdssinducedibdinmicebyregulatingtheintestinalmicrobiotamacrophageargininemetabolismaxis
AT bingpei resveratrolalleviatesdssinducedibdinmicebyregulatingtheintestinalmicrobiotamacrophageargininemetabolismaxis
AT yaqinzhang resveratrolalleviatesdssinducedibdinmicebyregulatingtheintestinalmicrobiotamacrophageargininemetabolismaxis
AT naijianwang resveratrolalleviatesdssinducedibdinmicebyregulatingtheintestinalmicrobiotamacrophageargininemetabolismaxis
AT zengxuwang resveratrolalleviatesdssinducedibdinmicebyregulatingtheintestinalmicrobiotamacrophageargininemetabolismaxis
AT feimao resveratrolalleviatesdssinducedibdinmicebyregulatingtheintestinalmicrobiotamacrophageargininemetabolismaxis