4.7 Article

Ruyi Jinhuang Powder accelerated diabetic ulcer wound healing by regulating Wnt/β-catenin signaling pathway of fibroblasts In Vivo and In Vitro

期刊

JOURNAL OF ETHNOPHARMACOLOGY
卷 293, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2022.115321

关键词

Diabetic ulcer; Ruyi Jinhuang powder; Wnt/beta-catenin; Wound healing; Fibroblast

资金

  1. National Natural Science Foundation of China [82004130]
  2. Shanghai Sailing Program [20YF1411900]
  3. Huadong Hospital Affiliated to Fudan University [2019jc015]

向作者/读者索取更多资源

Ruyi Jinhuang Powder (RJP) has significant therapeutic effects on diabetic ulcers as it promotes fibroblast proliferation and migration through activating Wnt/beta-catenin signaling pathway. In addition, RJP reduces inflammation and improves wound healing.
Ethnopharmacological relevance: Diabetic ulcer is a common complication of diabetes. Therapies of diabetic ulcer are still challenging due to the complicated aetiology. Ruyi Jinhuang Powder (RJP) is gradually adopted to treat diabetic ulcer and has a significant therapeutic effect. Aim of the study: To investigate the therapeutic potential for diabetic ulcer in vivo and in vitro, we explored whether and how RJP influences wound healing in mice and fibroblasts at the tissular, cellular and molecular levels. Materials and methods: The chemical composition of RJP was identified by HPLC. Streptozotocin (STZ) induced diabetic mice were used to confirm the curative effect of RJP in vivo. Besides, the impact of RJP in stimulating fibroblasts proliferation, migration and reducing inflammation was studied through CCK-8 assay, cell scratch assay, PCR, WB, etc. Results: A total of 17 compounds were identified in RJP by HPLC. Our data indicated that RJP promoted fi-broblasts proliferation and migration via activating Wnt/beta-catenin signaling pathway. Consistently, RNA-seq analysis of mice skin samples also showed that the shared differentially expressed genes (DEGs) between RJP group and control group were most enriched in wnt signaling pathway. These DEGs were closely related with wound repair. In addition, the anti-inflammation effect of RJP was also confirmed through downregulation of IL-1 alpha, IL-1 beta, IL-6 and IL-10 expression levels. These biological effects were reduced when the Wnt/beta-catenin signaling was blocked. The in vivo study also demonstrated the effect of RJP in improving epidermal wound closure, which was consistent with the in vitro results. Conclusions: Topical application of RJP was effective in treating diabetic ulcer. This research is helpful to provide new insights and evidence into the role of RJP in accelerating unhealing wound and reducing wound inflammation.

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