4.7 Article

Apple Polyphenols Improve Intestinal Antioxidant Capacity and Barrier Function by Activating the Nrf2/Keap1 Signaling Pathway in a Pig Model

Journal

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
Volume 70, Issue 24, Pages 7576-7585

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.2c02495

Keywords

apple polyphenols; finishing pigs; IPEC-J2 cells; intestinal antioxidant capacity; intestinal barrier function; Nrf-2/Keap-1 signaling pathway

Funding

  1. Sichuan Youth Science and Technology Innovation Research Team Project [2020JDTD0026]
  2. Sichuan Science and Technology Program [2021ZDZX0009]

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In this study, it was found that dietary supplementation of apple polyphenols improved intestinal barrier function and antioxidant capacity. The Nrf2/Keap1 signaling pathway was identified as the mechanism through which apple polyphenols promote intestinal health.
In recent years, the function of plant polyphenols to improve the intestinal barrier has been fully demonstrated. However, the exact mechanisms linking plant polyphenols with the intestinal barrier function have not yet been established. Apple polyphenols (APs) are safe and healthy nutrients, which are extracted from apples and their byproducts. Using pig and IPEC-J2 cell models, this study investigated the effects of dietary AP supplementation on intestinal antioxidant capacity and barrier function. Then, we further explored the role of the Nrf2/Keap1 signaling pathway in maintaining intestinal antioxidant capacity and barrier function. Our study found that dietary AP supplementation improved the intestinal mechanical barrier by promoting the intestinal morphology and intestinal tight junction protein expression, improved the intestinal immune barrier by increasing intestinal secretory immunoglobulin A production, and improved the intestinal biological barrier by increasing probiotics and decreasing the Escherichia coli population. Further research found that dietary AP supplementation increased the intestinal antioxidant capacity and activated the Nrf2/Keap1 signaling pathway. Finally, after treatment with Nrf2-specific inhibitor ML-385, the upregulation effect of APs on antioxidant capacity and tight junction protein expression was reduced in IPEC-J2 cells. Our results suggested that APs promoted intestinal antioxidant capacity and barrier function via the Nrf2/Keap1 signaling pathway.

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