亚麻籽油通过调节仔猪 LPS 挑战后的铁突变信号通路减轻肠道损伤

IF 4.5 2区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY
Junjie Guo, Xiaoqian Chen, Mohan Zhou, Xintian Yu, Huiling Zhu, Kan Xiao, Guoshun Chen, Yulan Liu
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引用次数: 0

摘要

范围事实证明,铁蛋白沉积在各种组织损伤和疾病中发挥着重要作用。亚麻籽油(FO)已被证实对肠道健康有益。本研究旨在探讨亚麻籽油是否能通过调节铁突变信号通路缓解脂多糖(LPS)诱导的肠道损伤:共 120 头断奶仔猪连续 4 周饲喂含 3% 大豆油 (SO) 或 3% FO 的日粮。试验结束后,从两个日粮处理组中选出 24 头仔猪,采用 2 × 2 因子设计,即油处理组(3% SO 与 3% FO)和 LPS 挑战组(生理盐水与 LPS)。注射 LPS 后 4 小时,宰杀 24 头仔猪并采集肠道样本。FO 可提高猪的生长性能。在 LPS 处理后,FO 可减轻肠道形态损伤和功能损伤。值得注意的是,FO 逆转了铁中毒的典型超形态和生化指标,包括谷胱甘肽、丙二醛和 4-羟基壬烯醛含量。从机理上讲,FO 可改善关键铁变态反应信号(包括转铁蛋白受体蛋白 1(TFR1)、重组铁应答元件结合蛋白 2(IREB2))的 mRNA 或蛋白质丰度的变化、FTL、HSPB1、铁蛋白重链 1 (FTH1)、铁蛋白 1 (FPN1)、SLC7A11、溶质运载家族 3 成员 2 (SLC3A2)、谷胱甘肽过氧化物酶 4 (GPX4) 和花生四烯酸-15-脂氧合酶 (ALOX15)。结论FO 可改善生长性能,减轻肠道结构和功能损伤,这与调节铁蛋白沉积信号通路有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Flaxseed Oil Attenuates Intestinal Damage by Regulating Ferroptosis Signaling Pathway Following LPS Challenge in Piglets

Flaxseed Oil Attenuates Intestinal Damage by Regulating Ferroptosis Signaling Pathway Following LPS Challenge in Piglets

Flaxseed Oil Attenuates Intestinal Damage by Regulating Ferroptosis Signaling Pathway Following LPS Challenge in Piglets

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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来源期刊
Molecular Nutrition & Food Research
Molecular Nutrition & Food Research 工程技术-食品科技
CiteScore
8.70
自引率
1.90%
发文量
250
审稿时长
1.7 months
期刊介绍: Molecular Nutrition & Food Research is a primary research journal devoted to health, safety and all aspects of molecular nutrition such as nutritional biochemistry, nutrigenomics and metabolomics aiming to link the information arising from related disciplines: Bioactivity: Nutritional and medical effects of food constituents including bioavailability and kinetics. Immunology: Understanding the interactions of food and the immune system. Microbiology: Food spoilage, food pathogens, chemical and physical approaches of fermented foods and novel microbial processes. Chemistry: Isolation and analysis of bioactive food ingredients while considering environmental aspects.
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