4.7 Article

Zuojin Pill attenuates Helicobacter pylori-induced chronic atrophic gastritis in rats and improves gastric epithelial cells function in GES-1 cells

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 285, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2021.114855

Keywords

Zuojin pill; Chronic atrophic gastritis (CAG); Helicobacter pylori(H.pylori); JMJD2B/COX-2/VEGF axis; HMGB1/NF-?B signaling pathway

Funding

  1. National Key R&D Program of China, China [2018YFC1704500]
  2. Science Foundation of Sichuan Education Department, China [18ZA0186]
  3. Xihua University Talent Introduction Project, China [Z211060]

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Zuojin pill (ZJP), a classical Chinese medicine formula, has therapeutic effects on Helicobacter pylori (H. pylori)-induced chronic atrophic gastritis (CAG). It lowers serum inflammatory markers, improves gastric tissue pathology, and reduces damage to gastric mucosal cells by inhibiting inflammation and modulating related signaling pathways.
Ethnopharmacological relevance: Zuojin pill (ZJP), a classical Chinese medicine formula, has been widely applied in Chinese clinical practice for the treatment of gastric injury such as acute gastric lesion, acute gastric mucosal injury, chronic unpredictable mild stress, gastroesophageal reflux disease, etc, thereby exerting anti-chronic atrophic gastritis (CAG) effects in traditional Chinese herbal medicine.& nbsp;Aim of the study: This study was aimed to explore the therapeutic effects and molecular mechanisms of ZJP on Helicobacter pylori (H. pylori)-induced CAG based on the comprehensive approaches.& nbsp;Materials and methods: Sprague-Dawley rats were infected with H. pylori for 8 weeks to establish CAG model. Then, rats in the ZJP groups received doses of 0.63, 1.26, and 2.52 g/kg ZJP for 4 weeks. Therapeutic effects of ZJP on serum indices and the histopathology of the gastric were analyzed in vivo. Moreover, GES-1 cells were infected with H. pylori to establish gastric epithelial cell injury model in vitro. Cell viability and gastric epithelial cell morphology were detected by a high-content screening (HCS) assay. Furthermore, the relative mRNA and protein expression of JMJD2B/COX-2/VEGF axis and HMGB1/NF-kappa B signaling pathway in vivo and in vitro were determined by RT-PCR and Western Blotting, respectively.& nbsp;Results: The results showed that the therapeutic effects of ZJP on CAG rats were presented in down-regulation serum biochemical indices and alleviating histological damage of gastric tissue. ZJP could dose-dependently decrease the serum IL-6, MCP-1, PGE2, TNF-alpha, and VEGF level and significantly improved gastric tissue inflammatory lesions. Besides, ZJP has an effect on increasing cell proliferation of GES-1 cells, ameliorating H. pylori-induced gastric epithelial cell damage. It was found that ZJP has a down-regulating effect on inflammatory reaction and could inhibit the relative mRNA and protein expression of JMJD2B/COX-2/VEGF axis and HMGB1/NF-kappa B signaling pathway in vivo and in vitro, including JMJD2B, COX-2, VEGF, VEGFR1, and VEGFR2, which in turn reduced the damage of gastric mucosal cells.& nbsp;Conclusions: The results suggested that ZJP exerts therapeutic effects on H. pylori-induced CAG by inhibiting the JMJD2B/COX-2/VEGF axis and HMGB1/NF-kappa B signaling pathway. These findings deeply explained why ZJP could be used to treat CAG clinically and clarified its pharmacological effect and potential mechanism in the treatment of CAG.

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