Evidence map›Paper›PMID 41126978›Full record

ArticleJournal of inflammation research2025

Isoorientin Modulates Gut Microbes and Their Metabolites to Alleviate Caco-2 Cell Monolayer Inflammation by Reducing Intestinal Permeability via P-Gp/eCBs.

Zhenzhen Wang, Yuang Jiang, Bensong Duan, Haibin Zhang, Aoxiang Li, Jin Yang, Mengke Lv, Jingya Yang

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Article in Journal of inflammation research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Zhenzhen WangCollege of Food Science and Technology, Shanghai Ocean University, Shanghai, 201306, People's Republic of China.
Yuang JiangCollege of Fisheries and Life Science, Shanghai Ocean University, Shanghai, 201306, People's Republic of China.ORCID 0009-0008-7832-6111
Bensong DuanDepartment of Gastroenterology Shanghai East Hospital, School of Medicine, Endoscopy Center, Tongji University, Shanghai, People's Republic of China.
Haibin ZhangDepartment of Gastroenterology Shanghai East Hospital, School of Medicine, Endoscopy Center, Tongji University, Shanghai, People's Republic of China.
Aoxiang LiCollege of Food Science and Technology, Shanghai Ocean University, Shanghai, 201306, People's Republic of China.
Jin YangCollege of Food Science and Technology, Shanghai Ocean University, Shanghai, 201306, People's Republic of China.
Mengke LvCollege of Food Science and Technology, Shanghai Ocean University, Shanghai, 201306, People's Republic of China.
Jingya YangCollege of Food Science and Technology, Shanghai Ocean University, Shanghai, 201306, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Isoorientin (ISO) is a naturally occurring flavonoid that studies have shown to have strong experimental antioxidant, anti-inflammatory, anti-diabetic and anti-obesity properties. It has been shown that ISO alleviates Dextran sodium sulfate (DSS) induced colitis in mice by modulating gut microbes and their metabolites. The aim of this study was to modulate gut microbes and their metabolism by ISO to investigate its anti-inflammatory effects and its specific molecular mechanisms in a lipopolysaccharide (LPS)-induced monolayer inflammation model in Caco-2 cells. Methods: Feces from ISO-treated DSS colitis mice were collected and gut flora culture supernatants were prepared. Detection of the effect of intestinal flora supernatants on the monolayer barrier of Caco-2 cells by inoculation of Caco-2 cells into the Transwell transmembrane culture system to simulate the intestinal mucosal barrier. Results: The results revealed that ISO-conditioned intestinal flora supernatant significantly increased TEER values, decreased intestinal epithelial FITC-dextran flux permeability, and restored LPS-induced occludin, ZO-1 protein expression in Caco-2 cells. Meanwhile, intestinal flora supernatant significantly ameliorated the LPS-induced inflammatory response. In addition, ISO further enhanced its protective effect on intestinal permeability by regulating the expression of P-glycoprotein (P-gp) and endogenous cannabinoid system (eCB)-related proteins, which may attenuate the inflammatory response by activating the P-gp/eCB signaling pathway. Conclusion: The present study offers fresh perspectives into the application of ISO-conditioned intestinal flora supernatant as a potential anti-inflammatory agent and intestinal barrier protector in vitro. The unique regulation of the P-gp/eCBs pathway by ISO-conditioned intestinal flora supernatant was the novel mechanistic insights provided in this study.

Indexed as

Caco-2 cellintestinal mucosal barrierisoorientinoccludinP-glycoproteinZO-1

Identifiers

PMID41126978
PMCPMC12537527

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