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Pterostilbene attenuates intrauterine growth retardation-induced colon inflammation in piglets by modulating endoplasmic reticulum stress and autophagy.
Chen, Yanan; Zhang, Hao; Li, Yue; Ji, Shuli; Jia, Peilu; Wang, Tian.
Afiliación
  • Chen Y; College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
  • Zhang H; College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China. zhanghao89135@163.com.
  • Li Y; Institute of Animal Science, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
  • Ji S; College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
  • Jia P; College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
  • Wang T; College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China. tianwangnjau@163.com.
J Anim Sci Biotechnol ; 13(1): 125, 2022 Nov 04.
Article en En | MEDLINE | ID: mdl-36329539
BACKGROUND: Endoplasmic reticulum (ER) stress and autophagy are implicated in the pathophysiology of intestinal inflammation; however, their roles in intrauterine growth retardation (IUGR)-induced colon inflammation are unclear. This study explored the protective effects of natural stilbene pterostilbene on colon inflammation using the IUGR piglets and the tumor necrosis factor alpha (TNF-α)-treated human colonic epithelial cells (Caco-2) by targeting ER stress and autophagy. RESULTS: Both the IUGR colon and the TNF-α-treated Caco-2 cells exhibited inflammatory responses, ER stress, and impaired autophagic flux (P < 0.05). The ER stress inducer tunicamycin and the autophagy inhibitor 3-methyladenine further augmented inflammatory responses and apoptosis in the TNF-α-treated Caco-2 cells (P < 0.05). Conversely, pterostilbene inhibited ER stress and restored autophagic flux in the IUGR colon and the TNF-α-treated cells (P < 0.05). Pterostilbene also prevented the release of inflammatory cytokines and nuclear translocation of nuclear factor kappa B p65, reduced intestinal permeability and cell apoptosis, and facilitated the expression of intestinal tight junction proteins in the IUGR colon and the TNF-α-treated cells (P < 0.05). Importantly, treatment with tunicamycin or autophagosome-lysosome binding inhibitor chloroquine blocked the positive effects of pterostilbene on inflammatory response, cell apoptosis, and intestinal barrier function in the TNF-α-exposed Caco-2 cells (P < 0.05). CONCLUSION: Pterostilbene mitigates ER stress and promotes autophagic flux, thereby improving colon inflammation and barrier dysfunction in the IUGR piglets and the TNF-α-treated Caco-2 cells.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Anim Sci Biotechnol Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Anim Sci Biotechnol Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido