Rutin attenuates zearalenone-induced ferroptosis of endometrial stromal cells in piglets through the p53 signaling pathway
文献类型： 外文期刊
作者： Wang, Chenlong 1 ; Chen, Chuangjiang 1 ; Wang, Mengya 1 ; Rahman, Sajid Ur 1 ; Wei, Bin 2 ; Ding, Hongyan 3 ; Huang, Wanyue 1 ; Wang, Xichun 1 ;
作者机构： 1.Anhui Agr Univ, Coll Vet Med, 130 West Changjiang Rd, Hefei 230036, Peoples R China
2.Huangyuan Cty Anim Husb & Vet Stn, Xining 812100, Qinghai, Peoples R China
3.Anhui Acad Agr Sci, Inst Anim Sci & Vet Med, Anhui Prov Key Lab Livestock & Poultry Prod Safety, Hefei 230031, Peoples R China
4.Anhui Prov Engn Lab Anim Food Qual & Biosafety, Hefei 230036, Peoples R China
关键词： ZEA; Rutin; ESCs; Ferroptosis; p53 signaling pathway
期刊名称：ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY （ 影响因子：6.1； 五年影响因子：6.4 ）
ISSN： 0147-6513
年卷期： 2025 年 290 卷
页码：
收录情况： SCI
摘要： Zearalenone (ZEA) is an environmentally widespread mycotoxin capable of posing a serious threat to food safety and public health, and porcine endometrial stromal cells (ESCs) are particularly sensitive to the toxic effects of ZEA. We hypothesized that Rutin, a flavonoid antioxidant, could significantly alleviate ZEA-induced ferroptosis through the p53 signaling pathway. In this study, we used porcine ESCs as a research model. When porcine ESCs were co-cultured with the addition of Rutin and ZEA following p53 gene silencing via siRNA transfection, Rutin significantly mitigated ZEA-induced mitochondrial damage, oxidative stress, and Fe2 + content through the p53 pathway. Additionally Rutin lowered the expression of p53, ALOX12, and ACSL4 while significantly improving cytokinesis, antioxidant enzyme activity, and SLC7A11, GPX4, Nrf2, FTH1, thereby inhibiting cellular ferroptosis. These findings suggested a novel programmed death mechanism for alleviating the cytotoxic effects of ZEA, involving the knockdown of p53.
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