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Narirutin mitigates dextrose sodium sulfate-induced colitis in mice by modulating intestinal flora.
- Source :
-
Phytomedicine : international journal of phytotherapy and phytopharmacology [Phytomedicine] 2024 Jul 25; Vol. 130, pp. 155730. Date of Electronic Publication: 2024 May 10. - Publication Year :
- 2024
-
Abstract
- Background: Ulcerative colitis (UC) is a prolonged inflammatory disease of the gastrointestinal tract. Current therapeutic options remain limited, underscoring the imperative to explore novel therapeutic strategies. Narirutin (NR), a flavonoid naturally present in citrus fruits, exhibits excellent anti-inflammatory effects in vitro, yet its in vivo efficacy, especially in UC, remains underexplored.<br />Objective: This work examined the effect of NR on dextrose sodium sulfate (DSS)-induced UC in mice in vivo, with a specific focus on the role of gut flora in it.<br />Methods: The effects of NR (10, 20, and 40 mg/kg) on DSS-induced UC in mice were investigated by monitoring changes in body weight, disease activity index (DAI) scores, colon length, and histological damage. Colonic levels of pro-inflammatory mediators, tight junction (TJ) proteins, and inflammation-related signaling pathway proteins were analyzed via enzyme-linked immunosorbent assay, western blot, and immunofluorescence. The role of gut microbiota in NR against colitis was analyzed through 16S rRNA sequencing, flora clearance assays, and fecal microbiota transplantation (FMT) assays.<br />Results: NR administration suppressed DSS-induced colitis as reflected in a decrease in body weight loss, DAI score, colon length shortening, and histological score. Furthermore, NR administration preserved the integrity of the DSS-induced intestinal barrier by inhibiting the reduction of TJ proteins (claudin3, occludin, and zonula occludens-1). Moreover, NR administration markedly repressed the activation of the toll-like receptor 4-mitogen-activated protein kinase/nuclear factor-κB pathway and reduced the amount of pro-inflammatory mediators in the colon. Importantly, the results of 16S rRNA sequencing showed that the intestinal flora of mice with colitis exhibited richer microbial diversity following NR administration, with elevated abundance of Lactobacillaceae (Lactobacillus) and decreased abundance of Bacteroidaceae (Bacteroides) and Shigella. In addition, the anti-colitis effect of NR almost disappeared after gut flora clearance. Further FMT assay also validated this gut flora-dependent protective mechanism of NR.<br />Conclusion: Our findings suggest that NR is a prospective natural compound for the management of UC by modulating intestinal flora.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier GmbH. All rights reserved.)
- Subjects :
- Animals
Mice
Male
Glucose metabolism
Colitis, Ulcerative chemically induced
Colitis, Ulcerative drug therapy
Dextran Sulfate
Flavanones pharmacology
Anti-Inflammatory Agents pharmacology
Disease Models, Animal
NF-kappa B metabolism
Fecal Microbiota Transplantation
Colitis chemically induced
Colitis drug therapy
Citrus chemistry
Tight Junction Proteins metabolism
Sulfates pharmacology
Gastrointestinal Microbiome drug effects
Colon drug effects
Colon pathology
Mice, Inbred C57BL
Subjects
Details
- Language :
- English
- ISSN :
- 1618-095X
- Volume :
- 130
- Database :
- MEDLINE
- Journal :
- Phytomedicine : international journal of phytotherapy and phytopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 38759313
- Full Text :
- https://doi.org/10.1016/j.phymed.2024.155730