丙二醛
脂多糖
铁蛋白
谷胱甘肽
谷胱甘肽过氧化物酶
抗氧化剂
脂质过氧化
GPX4
化学
超氧化物歧化酶
生物化学
生物
免疫学
酶
作者
Junjie Guo,Xiaoqian Chen,Mohan Zhou,Xin-Tian Yu,Huiling Zhu,Kan Xiao,Guoshun Chen,Yulan Liu
标识
DOI:10.1002/mnfr.202400199
摘要
Scope Ferroptosis has been demonstrated to play an important role in various tissue injuries and diseases. Flaxseed oil (FO) has been proven to have benefits for intestinal health. This study aims to explore whether FO relieved lipopolysaccharide (LPS)‐induced intestinal injury through modulating ferroptosis signaling pathway. Methods and results A total of 120 weaned piglets are fed diets with 3% soybean oil (SO) or 3% FO for 4 weeks. At the end of the trial, 24 piglets selected from two dietary treatment groups are used in a 2 × 2 factorial design with oil treatment (3% SO versus 3% FO) and LPS challenge (saline versus LPS). At 4 h postinjection with LPS, 24 piglets are slaughtered and intestinal samples are collected. FO improves growth performance of pigs. After LPS treatment, FO mitigates intestinal morphological damage and functional damage. Notably, FO reverses the typical ultra‐morphology and biochemical indexes of ferroptosis involving glutathione, malondialdehyde, and 4‐hydroxynonenal contents. Mechanistically, FO ameliorates the changes on mRNA or protein abundance of key ferroptosis signals including transferrin receptor protein 1 (TFR1), recombinant iron responsive element binding protein 2 (IREB2), FTL, HSPB1, ferritin heavy chain 1 (FTH1), ferroportin 1 (FPN1), SLC7A11, solute carrier family 3 member 2 (SLC3A2), glutathione peroxidase 4 (GPX4), and arachidonate‐15‐lipoxygenase (ALOX15). Conclusions FO improves growth performance and mitigates intestinal structural and functional damage, which is involved in regulating ferroptosis signaling pathway.
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