# Ziziphus jujuba Miller Ethanol Extract Restores Disrupted Intestinal Barrier Function via Tight Junction Recovery and Reduces Inflammation

**Authors:** Ye Jin Yang, Min Jung Kim, Ho Jeong Lee, Won-Yung Lee, Ju-Hye Yang, Hun Hwan Kim, Min Sup Shim, Ji Woong Heo, Jae Dong Son, Woo H. Kim, Gon Sup Kim, Hu-Jang Lee, Young-Woo Kim, Kwang Youn Kim, Kwang Il Park

PMC · DOI: 10.3390/antiox13050575 · 2024-05-07

## TL;DR

This study shows that an ethanol extract from Ziziphus jujuba Miller can help repair intestinal barriers and reduce inflammation in a model of inflammatory bowel disease.

## Contribution

The study demonstrates for the first time that Ziziphus jujuba Miller extract (ZJB) can restore intestinal tight junctions and reduce inflammation in IBD models.

## Key findings

- ZJB increased trans-epithelial electrical resistance by 61.389% and reduced permeability by 27.348% in Caco2 cells.
- ZJB reduced body weight loss, disease activity index, and colon shortening in DSS-induced IBD mice.
- LC-MS/MS identified seven active ingredients in ZJB, which up-regulated tight junction proteins like ZO-1 and occludin.

## Abstract

Inflammatory bowel disease (IBD) is a chronic inflammatory condition caused by the disruption of the intestinal barrier. The intestinal barrier is maintained by tight junctions (TJs), which sustain intestinal homeostasis and prevent pathogens from entering the microbiome and mucosal tissues. Ziziphus jujuba Miller (Z. jujuba) is a natural substance that has been used in traditional medicine as a therapy for a variety of diseases. However, in IBD, the efficacy of Z. jujuba is unknown. Therefore, we evaluated ZJB in Caco2 cells and a dextran sodium sulfate (DSS)-induced mouse model to demonstrate its efficacy in IBD. Z. jujuba extracts were prepared using 70% ethanol and were named ZJB. ZJB was found to be non-cytotoxic and to have excellent antioxidant effects. We confirmed its anti-inflammatory properties via the down-regulation of inflammatory factors, including inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). To evaluate the effects of ZJB on intestinal barrier function and TJ improvement, the trans-epithelial electrical resistance (TEER) and fluorescein isothiocyanate-dextran 4 kDa (FITC-Dextran 4) permeability were assessed. The TEER value increased by 61.389% and permeability decreased by 27.348% in the 200 μg/mL ZJB group compared with the 50 ng/mL IL-6 group after 24 h. Additionally, ZJB alleviated body weight loss, reduced the disease activity index (DAI) score, and induced colon shortening in 5% DSS-induced mice; inflammatory cytokines, tumor necrosis factor (TNF)-α, and interleukin (IL)-6 were down-regulated in the serum. TJ proteins, such as Zonula occludens (ZO)-1 and occludin, were up-regulated by ZJB in an impaired Caco2 mouse model. Additionally, according to the liquid chromatography results, in tandem with mass spectrometry (LC-MS/MS) analysis, seven active ingredients were detected in ZJB. In conclusion, ZJB down-regulated inflammatory factors, protected intestinal barrier function, and increased TJ proteins. It is thus a safe, natural substance with the potential to be used as a therapeutic agent in IBD treatment.

## Linked entities

- **Proteins:** NOS2 (nitric oxide synthase 2), COX2 (cytochrome c oxidase subunit II), TJP1 (tight junction protein 1), si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3), TNF (tumor necrosis factor), IL6 (interleukin 6)
- **Chemicals:** ethanol (PubChem CID 702), tumor necrosis factor (PubChem CID 44356648)
- **Diseases:** Inflammatory bowel disease (MONDO:0005265)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743] {aka COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2}, Ocln (occludin) [NCBI Gene 18260] {aka Ocl}
- **Diseases:** cytotoxic (MESH:D064420), IBD (MESH:D015212), weight loss (MESH:D015431), Inflammation (MESH:D007249)
- **Species:** Ziziphus jujuba (Chinese jujube, species) [taxon 326968], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** Caco2 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0025)

## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11118233/full.md

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Source: https://tomesphere.com/paper/PMC11118233