1. Academic Validation
  2. Caffeic acid improves intestinal barrier function integrity through activation of Nrf2 signaling pathway in weaned piglets and H2O2 induced IPEC-J2 cells

Caffeic acid improves intestinal barrier function integrity through activation of Nrf2 signaling pathway in weaned piglets and H2O2 induced IPEC-J2 cells

  • J Nutr Biochem. 2025 Sep:143:109952. doi: 10.1016/j.jnutbio.2025.109952.
Xueya Zhu 1 Tianlei Qiao 1 Zhiqing Huang 1 Gang Jia 1 Hua Zhao 1 Xiaoling Chen 2
Affiliations

Affiliations

  • 1 Animal Nutrition Institute, Key Laboratory for Animal Disease-Resistance Nutrition of China Ministry of Education, Sichuan Agricultural University, Chengdu, Sichuan, China.
  • 2 Animal Nutrition Institute, Key Laboratory for Animal Disease-Resistance Nutrition of China Ministry of Education, Sichuan Agricultural University, Chengdu, Sichuan, China. Electronic address: xlchen@sicau.edu.cn.
Abstract

Caffeic acid (CA), a common plant polyphenol, is considered to be a potentially powerful antioxidant and plays an important role in regulating intestinal barrier function. However, the underlying mechanism of CA in improving the intestinal barrier integrity and alleviating intestinal oxidative stress damage remains unclear. The aim was to study the effects of CA on the intestinal barrier function integrity of weaned piglets and hydrogen peroxide (H2O2) induced porcine intestinal epithelial cells (IPEC-J2 cells), and further explore its possible mechanism. The results of in vivo experiments showed that CA could significantly improve the growth performance and intestinal antioxidant capacity of piglets, improve the integrity of the jejunal mucosa, and reduce the incidence of diarrhea. The results of in vitro experiments showed that CA treatment effectively alleviated H2O2 induced oxidative stress in IPEC-J2 cells and increased the expression of key molecules in nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway. In addition, CA reduced the H2O2-induced increase of Lactate Dehydrogenase (LDH) release, and reversed the inhibition of H2O2 on tight junction related-proteins expressions and cell migration and increase in epithelial permeability in IPEC-J2 cells. However, the addition of Nrf2-specific inhibitor ML385 reversed the effect of CA. Taken together, CA could improve intestinal barrier integrity in weaned piglets, and it could alleviate H2O2-induced intestinal epithelial cell damage by activating Nrf2 signaling pathway.

Keywords

Caffeic acid; IPEC-J2 cells; Intestinal barrier function integrity; Nrf2 signaling pathway; Weaned piglets.

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