<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhu M</submitter><funding>National Guidance Foundation for Local Science and Technology Development of China</funding><funding>Guizhou Provincial Key Technology R&amp;amp;amp;D Program</funding><funding>Natural Science Special Research Fund of Guizhou University</funding><funding>Guizhou Provincial Basic Research Program (Natural Science)</funding><funding>National Natural Science Foundation of China</funding><funding>Guizhou Provincial Key Technology R&amp;D Program</funding><funding>Foundation of Key Laboratory of Animal Genetics, Breeding and Reproduction in The Plateau Mountainous Region, Ministry of Education, Guizhou University</funding><pagination>855</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10891758</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(4)</volume><pubmed_abstract>Deoxynivalenol (DON) is a common mycotoxin that is widely found in various foods and feeds, posing a potential threat to human and animal health. This study aimed to investigate the protective effect of the natural polyphenol piceatannol (PIC) against DON-induced damage in porcine intestinal epithelial cells (IPEC-J2 cells) and the underlying mechanism. The results showed that PIC promotes IPEC-J2 cell proliferation in a dose-dependent manner. Moreover, it not only significantly relieved DON-induced decreases in cell viability and proliferation but also reduced intracellular reactive oxygen species (ROS) production. Further studies demonstrated that PIC alleviated DON-induced oxidative stress damage by increasing the protein expression levels of the antioxidant factors NAD(P)H quinone oxidoreductase-1 (NQO1) and glutamate-cysteine ligase modifier subunit (GCLM), and the mRNA expression of &lt;i>catalase&lt;/i> (&lt;i>CAT&lt;/i>), &lt;i>Superoxide Dismutase 1&lt;/i> (&lt;i>SOD1&lt;/i>), &lt;i>peroxiredoxin 3&lt;/i> (&lt;i>PRX3&lt;/i>), and &lt;i>glutathione S-transferase alpha 4&lt;/i> (&lt;i>GSTα4&lt;/i>). In addition, PIC inhibited the activation of the nuclear factor-B (NF-κB) pathway, downregulated the mRNA expression of interleukin-1β (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor α (TNF-α) to attenuate DON-induced inflammatory responses, and further mitigated DON-induced cellular intestinal barrier injury by regulating the protein expression of Occludin. These findings indicated that PIC had a significant protective effect against DON-induced damage. This study provides more understanding to support PIC as a feed additive for pig production.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Piceatannol Alleviates Deoxynivalenol-Induced Damage in Intestinal Epithelial Cells via Inhibition of the NF-κB Pathway.</pubmed_title><pmcid>PMC10891758</pmcid><funding_grant_id>32202710</funding_grant_id><funding_grant_id>Qiankehe foundation-ZK [2022] General 159</funding_grant_id><funding_grant_id>2023-009</funding_grant_id><funding_grant_id>QJH-KY [2020] 257</funding_grant_id><funding_grant_id>QKHZC-2021-General 147</funding_grant_id><funding_grant_id>Gui Da Te Gang He Zi [2020] 24</funding_grant_id><pubmed_authors>Zhu M</pubmed_authors><pubmed_authors>Zhang YY</pubmed_authors><pubmed_authors>Liu GW</pubmed_authors><pubmed_authors>Cheng YJ</pubmed_authors><pubmed_authors>Lu EQ</pubmed_authors><pubmed_authors>Huang K</pubmed_authors><pubmed_authors>Xu E</pubmed_authors><pubmed_authors>Fang YX</pubmed_authors><pubmed_authors>Wang XJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Piceatannol Alleviates Deoxynivalenol-Induced Damage in Intestinal Epithelial Cells via Inhibition of the NF-κB Pathway.</name><description>Deoxynivalenol (DON) is a common mycotoxin that is widely found in various foods and feeds, posing a potential threat to human and animal health. This study aimed to investigate the protective effect of the natural polyphenol piceatannol (PIC) against DON-induced damage in porcine intestinal epithelial cells (IPEC-J2 cells) and the underlying mechanism. The results showed that PIC promotes IPEC-J2 cell proliferation in a dose-dependent manner. Moreover, it not only significantly relieved DON-induced decreases in cell viability and proliferation but also reduced intracellular reactive oxygen species (ROS) production. Further studies demonstrated that PIC alleviated DON-induced oxidative stress damage by increasing the protein expression levels of the antioxidant factors NAD(P)H quinone oxidoreductase-1 (NQO1) and glutamate-cysteine ligase modifier subunit (GCLM), and the mRNA expression of &lt;i>catalase&lt;/i> (&lt;i>CAT&lt;/i>), &lt;i>Superoxide Dismutase 1&lt;/i> (&lt;i>SOD1&lt;/i>), &lt;i>peroxiredoxin 3&lt;/i> (&lt;i>PRX3&lt;/i>), and &lt;i>glutathione S-transferase alpha 4&lt;/i> (&lt;i>GSTα4&lt;/i>). In addition, PIC inhibited the activation of the nuclear factor-B (NF-κB) pathway, downregulated the mRNA expression of interleukin-1β (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor α (TNF-α) to attenuate DON-induced inflammatory responses, and further mitigated DON-induced cellular intestinal barrier injury by regulating the protein expression of Occludin. These findings indicated that PIC had a significant protective effect against DON-induced damage. This study provides more understanding to support PIC as a feed additive for pig production.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2026-07-03T03:15:06.822Z</modification><creation>2026-07-03T03:10:17.298Z</creation></dates><accession>S-EPMC10891758</accession><cross_references><pubmed>38398607</pubmed><doi>10.3390/molecules29040855</doi></cross_references></HashMap>